Wednesday, July 7, 2010

Looking at cilia

 
In a recent article in The Scientist, Peter Satir points out that the cilium was the very first distinct organelle ever directly observed by scientists--van Leeuwenhoek noted their existence in the 1660s.  But we are only now starting to fully understand these amazing and vital structures.

Until only the last decade or so, we thought that cilia were organs of cell motility--period.  But as I've noted in recent editions of my textbooks (e.g. Anatomy & Physiology, p.82-83), we now know that cilia play a critical role in a cell's ability to sense its surroundings.

Not only is this sensory function useful for, well, er, mediating senses such as hearing and equilibrium, it's also critical for cells to figure where to go (and when) during embryonic development.  In fact, it's been shown that situs inversus (the condition in which internal organs are flipped in their left-right orientation) is caused by a mutation affecting the structure of the primary cilium of developing cells in the embryo.

Cilia, it turns out, are centrally involved in a lot of different cell functions.

If you want a quick and interesting review of the history of cilia from one of the pioneers in cilia research, including answers to "why do we have to learn this stuff if I'm going to be a [insert health profession here]?," then check out this article:
Eyelashes Up Close
Peter Satir
The Scientist Volume 24 | Issue 7 | Page 30 2010-07-01
[Brief, well-illustrated review of what we know about cilia so far.  Includes great graphics and useful references.]
For more FREE images of cilia you can use in your course, see The A&P Professor website's FREE Image Library of Cell Structures.
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Monday, June 7, 2010

Sex differences in body fat distribution

When discussing sex differences in body fat distribution in my A&P course, I off-handedly refer to the roles of sex hormones in regulating the development that leads to these differences.  But how much do we really know about how that works?  Some recent work sheds a bit of light on that.

For example, a research review recently appearing in Obesity Reviews shows that indeed estrogen is responsible for promoting fat deposition in adult women.

Another recent article, this one in The International Journal of Obesity, suggests that there is a huge difference between the gene activity in male fat vs. female fat.  That is, the anatomy and physiology of male fat and female fat differs far more than anyone has yet realized.

Why Do Women Store Fat Differently From Men?.
University of New South Wales.
ScienceDaily 4 March 2009. 17 May 2010
[Brief synopsis of a research review from Obesity Reviews]

Does oestrogen allow women to store fat more efficiently? A biological advantage for fertility and gestation
A. J. O'Sullivan
Obesity Reviews Volume 10, Issue 2, Date: March 2009, Pages: 168-177
[Research review]

Belly Fat or Hip Fat: It Really Is All in Your Genes, Says Researcher.
UT Southwestern Medical Center.
ScienceDaily 16 May 2010. 17 May 2010

A microarray analysis of sexual dimorphism of adipose tissues in high-fat-diet-induced obese mice. 
K L Grove, et al.
International Journal of Obesity, 2010; DOI: 10.1038/ijo.2010.12
[Research article]

Sunday, May 30, 2010

FREE image of cerebral tracts

I recently posted a new image to the FREE Image Library at The A&P Professor website.  This one is an amazing map of white matter tracts in the cerebrum that was made using MRI (magnetic resonance imaging) tractography.  Click on the thumbnail to see the large version of the image (and the source with copyright/use info).

This image could be used in a PowerPoint slide in your class to make a dramatic point about the structure and function of the brain, eh?

If you want some background on how this image was made:
Estimating the Confidence Level of White Matter Connections Obtained with MRI Tractography.
Gigandet X, Hagmann P, Kurant M, Cammoun L, Meuli R, et al. 
PLoS ONE 2008 3(12): e4006. 
doi:10.1371/journal.pone.0004006 

Want more information on the FREE Image Library at The A&P Professor website . . . and tips on how to use it?  See my recent article in this blog.

Thursday, May 27, 2010

New blog feature


This blog now has a new feature . . . AnswerTips. If you double-click any word or phrase in this blog, a floating box will appear with additional information.

You can use this handy feature to:
  • look up the meaning of an unfamiliar term
  • find the acronym or abbreviation of a term (or, conversely, find the meaning of the acronym)
  • get a written and audio pronunciation guide for a term
  • find the word origin and word parts of a term
  • find related links
Try it right now by clicking this term . . . erythropoietin (used in a recent blog posting).

Now try it on ANY other word in this or any other post on this blog.

Yes . . . I've also added this feature to The A&P Professor website that serves as a resource-rich companion to this blog.

Oh, and another thing . . .YOU can add this feature to your online syllabus, class notes, blog, wiki, or other online resource for FREE!  It's incredibly easy. You can automatically and instantly give your students access to audio pronunciations (especially useful for ESL students) and definitions to unfamiliar terms.

If you want to see how that works, check out this example from my course website: Learning Outline for Skin.

And did I mention that AnswerLink is free? 

Just go to http://my-ap.us/bwkmpX to learn more.

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Saturday, May 22, 2010

Latest in blood doping

The subject of blood doping has come up a few times in this blog.  Recently, we heard the latest in the Floyd Landis blood doping story . . . now, after years of vigorous (and costly) denials, cycling champion Landis has now admitted that he DID dope to prepare for competitions.

Landis states the he used EPO (erythropoietin) to increase his hematocrit to improve performance during cycling events.(EPO is pictured here.)

He has also stated that Lance Armstrong, another champion cyclist, gave him EPO and discussed his own blood doping experiences with Landis.  Armstrong denies these claims.

Listen to the story from NPR:

I have an article on doping at The A&P Professor website that includes a lot of resources, as well as tips on using the topic of doping to engage students in a deeper understanding of human structure and function.
Doping
K. Patton
The A&P Professor, accessed May 21, 2010
[Tips and resources regarding doping for A&P courses.]
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Thursday, May 20, 2010

Artificial life?

Once they "get" the basic idea of molecular genetics, my A&P students become fascinated with those teeny-weeny molecules can have such huge impacts on the structure and function of the body.  On the drive home from campus today, I heard a great story on NPR about the announcement by Craig Venter that his team has successfully created a living, reproducing cell using completely synthetic DNA.  

They did this by using yeast cells to assemble smaller, synthesized bits of DNA and transferring it to living cells, which then reproduced the genome in offspring cells. 

While this is a long way from the claims (and concerns) of "creating artificial life," it is a huge discovery.

If you want to hear more about this, listen to the story yourself at Scientists Reach Milestone On Way to Artificial Life.

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Monday, May 17, 2010

Encouraging students to start their library

Today, I posted an entry at The A&P Student blog encouraging students to begin a personal library of professional books.  I encouraged them to start with their A&P textbook.

Many students sell their textbooks back to the bookstore as a regular thing . . . without stopping to realize that SOME textbooks should be going into their individual professional library.
 
A professional library is the set of references that a student can begin to build NOW and continually add to throughout their professional career. Such individual libraries serve as indispensable tools to help professionals survive and excel in a health-related career.

For health professionals, the A&P textbook will be needed for  upcoming health professions courses and clinicals/practicums. It will also serve well later, when students finally begin their careers.

You may want to post one or more of these links to share with your students:
[Recent blog post from The A&P Student]
[Blog post from The A&P Student from May 2009]

[Brief article from my Lion Den collection of Study Tips and Tools]


Thursday, April 1, 2010

Nature and Science to merge?

Will it be called Natural Science or Science Nature?   You can vote on it when the esteemed journals Science and Nature combine to form a new, open-access journal.

Want to know more?

Science, Nature Team Up on New Journal
John Travis
Science NOW, 1 April 2010

I hope you all have a crazy April 1!

Friday, February 26, 2010

Crazy artificial genetish

This is just crazy.  I'm still not decided whether it's mad-scientist, what-could-they-possibly-be-thinking? crazy or it's brilliant, why-didn't-they-think-of-this-sooner, life-is-now-complete crazy.

According to a recent post at TheScientist.com, scientists have recently created an artificial system in which a bizarre, created ribosome reads codons in mRNA that are four bases long. You read the correctly . . . instead of reading bases three at a time (like in real life), these little monsters can read a whole different form of genetic language—or genetish, as author Matt Ridley calls it.

This breakthrough allows scientists to build a whole new system of creating proteins—one in which there could be up to 256 different possible amino acids available.  This means that instead of being limited to using only the 22 naturally-occurring amino acids currently available for playing around to produce crazy new proteins, scientists can now also use synthetically modified amino acids with a variety of chemical properties. Modified or synthetic amino acids have no 3-base codons to represent them in natural genetish.

Just a few months ago, we were lauding the Nobel laureates who helped us figure out the structure of the ribosome.  Now we're seeing the creation of artificial ribosomes that translate artificial genetish. I guess this is a huge breakthrough for chemists hoping to synthesize new types of proteins.  It may also provide opportunities for synthetic biologists (scientists attempting to create artificial cells, tissues, and organisms).  It certainly is a great starting point for a sci-fi novel!

Want to know more?

Genetic coding revamp
Jef Akst
TheScientist.com 14 Feb 2010
[Summary of development of a new genetic language.]

Some background from the primary literature:

A chemical toolkit for proteins — an expanded genetic code
Jianming Xie et al.
Nature Reviews Molecular Cell Biology 7, 775-782 (October 2006) doi:10.1038/nrm2005


An evolved ribosome for genetic code expansion
Caroline Köhrer et al.
Nature Biotechnology 25, 745 - 746 (2007) doi:10.1038/nbt0707-745


A network of orthogonal ribosome·mRNA pairs
Oliver Rackham et al.
Nature Chemical Biology 1, 159 - 166 (2005) doi:10.1038/nchembio719

Monday, February 22, 2010

FREE digestion images

http://bit.ly/ciKu0T
Although there's still a lot more to go, I have recently updated the library of images for digestion in the FREE Image Library at The A&P Professor website.


In a previous post I outlined a few of the many ways you could use supplemental images like these.  In this batch, there are some dramatic images of gall stones, laparoscopic views of digestive organs that I may use to spice up our classroom discussions a bit.

Thursday, February 18, 2010

New discovery about sperm's ability to swim

Scientists have found the trigger that gets sperm swimming in the female reproductive tract.

Sperm cells in the testis are pretty quiet . . . they don't seem very interested in swimming.  However, after they are ejaculated into the female reproductive tract they become activated and get with the program. We already knew that the sperm cells need to raise their pH in order to kick into their swimming mode . . . but we didn't know how that is actually done.

In an article in the journal Cell, researchers report that they have the answer . . . one-way proton (H+) channels called Hv1 that open when sperm enter the female reproductive tract.  Increasing the intracellular pH triggers the influx of calcium ions, which in turn activate the sperm flagellum.  And they're off!

The increase in intracellular sperm pH also enables the sperm's acrosome to become activated and get ready to do its job, too.

Hv1 may be a key to triggering the hyperactivation and capacitation of sperm necessary for male fertility.

The researchers also found that a chemical similar to the active ingredient in marijuana inhibits the Hv1 channels and thus reduced fertility.  Perhaps this explains low fertility among males who are chronic users of marijuana.  And perhaps this opens the door to discovering chemicals that can be used to regulate the sperm fertility.

Want to know more?
Science News web edition : Thursday, February 4th, 2010
[Summary article includes a cool fluorescent micrograph.]

Acid extrusion from human spermatozoa is mediated by flagellar voltage-gated proton channel. 
Lishko, P.V. et al.
Cell Volume 140, Issue 3, 327-337, 5 February 2010
[Original research article with some fabulous images in the graphical abstract and an excellent movie that features the scientists explaining their discovery. ]

Sunday, February 14, 2010

Any dopes in Vancouver?


If you're like me, I mention the concept of blood doping when covering the life cycle of red blood cells (RBCs) and the homeostatic mechanisms that regulate the population numbers of RBCs.

In 2008 and 2009,  beginning around the time of the Beijing Olympics, I wrote a series of articles on doping in this blog and an extended version at The A&P Professor website.

I recently updated that extended doping article with a link to a recent news story from the Canadian Press service regarding the possibility of doping with the experimental anemia drug Hematide.

The doping issue is a great way to tie an unfortunately unending series of "real life" high-profile cases to the concepts of blood physiology.

Check out my Doping article, which includes several resources from major anti-doping agencies plus hints for incorporating doping issues in your A&P course.

You may also be interested in the PBS video Doping for Gold, which chronicles doping in a generation of European athletes. In the 1970s, female East German athletes came from nowhere to dominate international sport. Behind their success lay a secret, state-sponsored doping program that distributed untested steroids to athletes as young as 12. Many of these girls had no knowledge that they were being doped, and now, their damaged bodies and psyches deal with the cruelty of a government that pursued international glory at the expense of its most acclaimed citizens.

Wednesday, February 10, 2010

Prions are our friends

OK, let's see if I can remember what I just read about prion proteins (PrPs) . . . I think I read that they can help us store memories.  Oh yeah, that's right . . . and it turns out that they are needed to maintain the insulating myelin sheath around neurons that enables proper conduction of action potentials.

In my Anatomy & Physiology textbook I define a prion as
a term that is short for “proteinaceous infectious particles,” which are proteins that convert normal proteins of the nervous system into abnormal proteins, causing loss of nervous system function; the abnormal form of the protein also may be inherited; a newly discovered type of pathogen, not much is known about how the prion works; see bovine spongiform encephalopathy, variant Creutzfeldt-Jakob Disease (vCJD)


Well, it turns out that prions are not all bad, after all.  In a recent article in Nature Neuroscience, scientists report that certain prions are needed for the axonal signaling to Schwann cells that is needed to maintain the myelin sheath (pictured) and thus maintain normal conduction of nerve impulses.

In another finding reported in the journal Cell, scientists working with prions in sensory neurons of the sea slug found that the clumping of prions that we previously associated only with prion diseases plays a role in preserving memory.  Typically, when prions clump, they for tangles called amyloid plaques in a cell. Apparently, the clumping of certain prions at synapses increase the length of time that a memory is stored at that synapse.

Researchers also found that the neurotransmitter serotonin promotes the formation of the memory-preserving clumps.

More work needs to be done, of course, but these findings may lead to the discovery of a central role for prions in retaining long-term memories.

Want to know more?
Axonal prion protein is required for peripheral myelin maintenance. 
Bremer, J., et al.
Nature Neuroscience. 24 January 2010. doi:10.1038/nn.2483
[Original research article]

Prion protein is not all bad
Tina Hesman Saey
Science News February 13th, 2010; Vol.177 #4 (p. 17) 
[Summary article describing the role of prions in maintaining the myelin sheath, as well as some general insights on the emerging new view of prions.]
Aplysia CPEB Can Form Prion-like Multimers in Sensory Neurons that Contribute to Long-Term Facilitation
Kausik Si, et al.
Cell Volume 140, Issue 3, 421-435, 5 February 2010
[Original research article included a nifty graphical summary of the central findings.]
Click here for an audio interview with the scientist about this breakthrough

Protein clumps like a prion, but proves crucial for long-term memory
Tina Hesman Saey
Science News web edition : Thursday, February 4th, 2010
[Summary article explaining new research findings and their importance.]

Saturday, February 6, 2010

FREE respiratory images


You already know that I'm slowly adding to the Free Image Library at The A&P Professor website.  I've recently added a few images related to the Respiratory System to the collection.

All the images are either copyright-free or provide a free license to re-use them with permission.  So you can use them to . . .
  • Add them to your PowerPoint slides.

  • Use them in handouts or outlines.

  • Use them in tests or worksheets. Many of them have numbered and/or unlabeled versions that make this easy for you.

  • Provide them to students to use for their reports, projects, or concept maps.

  • Use them as icons for your website or learning management system.

  • Illustrate case studies with medical images or clinical procedures.

  • Use pathology images to hammer home concepts of normal anatomy and physiology.

  • Make your own anatomy T-shirts using iron-on transfer paper to print the images.

  • Receive inspiration to become a scientific illustrator.  (Then call me, I can use your help!)
Why not just use the images provided by the publisher of your textbook?
  • No textbook contains all the variations of how to draw a structure or concept.  Use alternate images to help drive home a particular point.

  • Students aren't really learning their anatomy and physiology if they memorize a particular diagram.  Using alternate diagrams on worksheets and tests pushes them to learn where things really are in the body. . . not where they happen to be labeled in the book.

  • Textbooks must conserve space to remain a practical tool.  There are many images that would be great to show students . . . such as medical images, portraits of A&P heroes or sources of eponyms, or amazing micrographs . . . that are simply not appropriate for a beginning-level textbook.


This image of an iron lung is not appropriate for a textbook, perhaps, but it might help you explain the concept of how pressure affects the mechanics of breathing.

Please send me your ideas for images that you need (maybe I can find them for you).

I'll be updating you when I add more topics to the Free Image Library.

If you have any suggestions for additional subjects for images, let me know and I'll try to find them for you.

Tuesday, February 2, 2010

Lipid rafts


Having lived most of my life near the river banks at the confluence of the Mississippi and Missouri Rivers, I guess I have a special place in my heart for rafts. A few years ago, when scientists discovered organized domains within cell membranes and named them rafts, I guess it all felt pretty obvious to me . . . and comfortable.

I was thinking about rafts today when I received this month's issue of  The Scientist, which features a cover story on the evolution of the lipid raft concept.

My Life on a Raft
Kai Simmons
The Scientist Volume 24 Issue 2  Page 24 February 2010
[Brief article by a pioneer in the discovery and study of lipid rafts]

In my textbook Anatomy & Physiology I define a membrane raft as . . .
"a structure made up of groupings of molecules (cholesterol, certain phospholipids, proteins) within a cell membrane that travel together on the surface of the cell, something like a log raft on a lake; also called lipid raft"
 When I first added the concept of lipid rafts to our introductory chapter on cellular structure a number of years ago, some of my colleagues were a bit put off by this addition.  Some reviewers suggested that I drop it because it wasn't, well, standard in the texts with which they were familiar.

First, I think that when we form our own cohesive idea of what a cell is, it's hard to break that apart easily to accommodate changes and (especially) radical new concepts.  It's even harder to imagine that any new concepts of cell structure and function have any place in an introductory conversation about cells. 

Second, it isn't always immediately clear that a beginning student is really going to encounter significant applications of such a new concept in their studies . . . or in their practice.

With lipid rafts, the concept was used several times in other parts of the book to understand such central ideas as endocytosis.  As a science, we continue to learn about significant medical application opportunities, such as a possible effective therapy for HIV infection and other viral conditions (for example, see New non-drug fix for HIV).

Similarly, come colleagues question my textbook's coverage of the cytoskeleton and motor molecules, when this dynamic system seems to play a basic, central (and increasingly well understood) role in many mechanisms typically covered in a beginning A&P course . . . not to mention applications in clinical science.

So updating a textbook can be quite challenging when it comes to deciding how to handle new ideas that come along. 

When, if ever, is a new biological concept ready to be put into an introductory textbook?  If one puts it in early, then some users are alienated by the unfamiliar.  Some may even be suspect of something different than the orthodox and time-tested A&P curriculum. If one waits until everyone has already become familiar with the new idea, then isn't it a bit late to be first introducing into a textbook?

For me, the central question is, "Do textbook authors have any responsibility to introduce new concepts into the curriculum?"   I think the answer is yes.  Of course, curriculum issues are guided by more than just textbook content.  Many agents interacting on many levels help guide the evolution of curriculum in anatomy and physiology (and any other discipline).  I think textbook authors are in an unusual . . . and sometimes scary . . . position of offering some of the latest ideas available.

Of course, introducing additional concepts has to be balanced with the concern that too much information, no matter how up-to-date or relevant, may make it hard for the beginning learner to establish a meaningful foundation upon which to build later, fuller understanding of human structure and function.  Another difficult and scary task, then, is to determine what is essential at the beginning level and what can be held off for a later time when the additional information will be more easily incorporated into a student's understanding.


I'd love to hear your comments!   What is the role of the textbook author when in comes to incorporating new or changed concepts in the A&P curriculum?  How can one determine which concepts are better left for later learning?

NOTE: Get some FREE images of lipid rafts to use for your class at The A&P Professor FREE Image Library.

Wednesday, January 27, 2010

FREE Neuroscience Workshop at Univ of Missouri



Those of you with easy access to the heart of America (Missouri) may be interested in the

Fourth Annual Summer Workshop on ‘Experiments and Models for Teaching Undergraduate Neuroscience’, 4-6 Aug 2010

I attended this workshop the summer before last a had a great time . . . and I learned a lot.  Besides some interesting perspectives and a really cool earthworm-based lab experiment I was able to expand my network of other colleagues interested in learning better ways to teach.  Besides the actual hands-on learning and demonstrations, you'll get a rare chance to observe the recordings of action potentials in a state of the art neuroscience laboratory.


The University of Missouri—Columbia (MU) Colleges of Engineering and Biological Sciences are sponsoring this two-day workshop focused on novel curriculum development in neuroscience that will be held Wednesday, Thursday, and Friday, August 4, 5 & 6, 2010, on the Columbia campus. The Workshop is targeted to undergraduate faculty from biological sciences, psychology, physics and engineering with an interest in teaching and learning more about neuroscience.

The workshop was initiated by a National Science Foundation grant to MU to develop undergraduate curriculum in the area of computational neuroscience. This is the fourth time we are offering this annual workshop, incorporating input from past years.

For more information, go to
http://engineering.missouri.edu/neuro/outreach-programs/neuro-workshop.php

If you are interested in applying to the workshop, send an email stating your interest to my new friend Satish Nair at MU: NairS@missouri.edu

FREE cardio images for your A&P course

Although the images in the textbook I use are excellent, I often want to supplement my presentations or outlines with additional images.  

For example, a photo of Karl Landsteiner working in his lab can add a bit to the discussion about blood types.  An unlabeled heart diagram might be just the thing I need to add an alternate question to my online test bank.  Dramatic micrographs, medical images, and animations can spark and hold the interest of my students.

I've recently added a few more FREE images to the Image Library at The A&P Professor website in these areas:
Click on any link above to get to these images.

This is a work in progress, so I don't have a huge number of images yet.  Check back frequently to look for more images as I add them.

If you have any additional images to suggest, send the source URL to me and I'll add it.  If you have images of your own that you are willing to donate to the image library, let me know that, too.  Just contact me at kevin@theapprofessor.org

Sunday, January 24, 2010

Now's the time for FREE student bookmarks!


It's time once again to get our students thinking about ways to organize their time and implement some study strategies and learning shortcuts so they can survive and thrive in a new semester of A&P.

What better way to start a new semester than with the blog that's all about student survival and success . . . The A&P Student?

Just send them to theAPstudent.org for tips, tricks, resources, and secrets to success in A&P.

To help them find it (and remember it) . . . and start off the semester by giving them gifts . . . why not order some FREE eyeball bookmarks to give them?  Just go to the EYEBALL BOOKMARK page at The A&P Professor to order yours now!

Even if your students don't use the blog with all the FREE learning resources, at least they'll have a cool anatomy bookmark to use, eh?

And don't forget to tell them about the handy Survival Guide For Anatomy And Physiology: Tips, Techniques And Shortcuts

More graduate biology courses at the HAPS Conference


OK, so you missed out on that cool cadaver class presented by HAPS Institute (HAPS-I) in San Diego this winter . . . because it filled up faster than I could tell you about it!  But now's your second chance for some great graduate biology courses especially for teachers of human anatomy and physiology courses:

1. Advances in Anatomy and Physiology 2010  (Ellen Arnestad and Kevin Patton)

2. Advanced Cardiovascular Physiology: The Heart at Work and at Rest (Robert Carroll)

3. Concepts in Human Embryology (Valerie O'Loughlin)

4. Molecular and Cellular Basis of Disease (Kelly McDonald)
These are great courses that feature both useful content about human A&P and experience with best practices in teaching these subjects.  These are courses that are MEANINGFUL to what you do every day in your own teaching.  And you'll be there with folks just like you . . . who teach secondary, college, and university A&P.

Each course earns you 2 graduate credits from the Biology Department of the University of Washington (Seattle). 

These courses begin with online work on April 13, involve seminars and/or workshops during the Denver HAPS Conference (May 29 - June 3), and continue with online work through August 19.  Each syllabus has additional details.  Conference registration (plus lodging, meals, and transportation, if needed) is required (in addition to HAPS-I course fees). 

Want to know more? 

Remember . . . THESE COURSES FILL EARLY.  So you want to get on this ASAP.  I mean it this time!

In fact, some spots have already been taken by past HAPS-I Scholars and by members of the HAPS-I Update email list, who all received notice of these course openings a few days ago.  (If you want prior notice of HAPS-I courses, go to http://www.hapsweb.org/displaycommon.cfm?an=1&subarticlenbr=234 to subscribe to either the HAPS-I Scholars Google Group or the HAPS-I Update Google Group.)

Registration is now open at http://www.hapsweb.org/displayconvention.cfm?conventionnbr=7898

For more information on the HAPS Annual Conference in Denver, go to http://www.hapsweb.org/displayconvention.cfm?conventionnbr=7450

EARLY BIRD CONFERENCE RATES APPLY UNTIL 2/1/2010!

Wednesday, December 9, 2009

Another posterior pituitary hormone


A recent paper in the Proceedings of the National Academy of Science shows that that the posterior pituitary (neurohypophysis ) secretes another hormone besides antidiuretic hormone (ADH; vasopressin) and oxytocin (OT).  It is the hormone secretin.

Secretin is already known to be secreted from the intestinal lining, having a variety of effects in regulating stomach and pancreatic function during the digestive process.  New findings indicate, however, that secretin is also secreted by the posterior pituitary.

Neurohypophysial release of secretin is triggered by plasma hyperosmolality—as in dehydration of the body. Secretin then promotes the expression and release of ADH, which in turn promotes water conservation by the kidney.  Secretin also appears to have direct water-conserving effects in the kidney as well.

Want to know more?

Secretin as a neurohypophysial factor regulating body water homeostasis
Jessica Y. S. Chu, et al. 
Proceedings of the National Academy of Science  September 15, 2009 vol. 106 no. 37 15961-15966 
doi: 10.1073/pnas.0903695106
[Abstract of the recent paper.]

Highlights From The Literature
Physiology 2009 24:322-324
doi:10.1152/physiol.00037.2009
[Summary of the significance of this discovery.] 


Click here for a FREE 3D see-through image of the pituitary's location that you can use in your course.

Too late for cadaver class!


I had hoped to tell you all about a great new course offered by HAPS Institute . . . Anatomy of the Abdomen and Thorax . . . but it filled up in less than half a day!

Lucky for us (and the dozen or so folks on the waitlist), this is the first in a series of several courses that center around a weekend workshop in a cadaver lab with expert dissectors.

The Anatomy of the Abdomen and Thorax course held in February in San Diego is just the first in a series of courses that will be held at various locations in North America in the coming months and years.

These courses carry three graduate credits from the University of Washington (Seattle) biology department. All HAPS-I courses are meant for folks who already teach anatomy and physiology (high-school through graduate levels) fill in their background in various topics within human biology . . . or simply to brush up on the lastest concepts.  Even if you already have a graduate degree and "don't need the credit" you'll find these courses to be both fun and useful.

All HAPS-I courses also involve emerging methods of active learning and thus showcase methods of teaching and learning that participants can adapt into their own courses.

Want to know more about HAPS-I and its courses? Click here for more information.

However, when new HAPS-I courses open up . . . ACT QUICKLY because they DO fill quickly!

Sunday, November 8, 2009

Bacterial microbiomes on human skin

Nearly a year ago, I shared results of a study of the bacteria that live on human skin, including these fun facts:
  • Females have a higher diversity of bacteria on their hands than males . . . perhaps due to a slightly higher skin pH in women, or perhaps the mix of sebum, sweat, and lotions, or maybe even hormonal differences . . . they couldn't really say for sure at this point
  • Females have more bacteria living under the surface film of skin than males
  • 4, 742 different species of bacteria were found in the whole group of subjects
  • The species each of has on our hands is a rather unique mix--only 5 (out of 4,742) species were found on every hand in the group
  • Most of the 150 or so different species of bacteria found on skin of an individual hand are beneficial or harmless . . . only a small minority are pathogenic
  • The diversity of bacteria differs between a person's right hand and left hand
  • Hand washing (as practiced in this group) did not remove many of the bacteria (or the populations recovered rapidly after washing)
Recently, another study was published that gives us an even more complete picture of the micro-ecology of human skin.  The report, published online a few days ago by the journal Science, provides an inventory of what organisms live where on the human skin.

A few fun facts about the bacteria, viruses, and fungi of the human skin gleaned from the new study:
  • Microbes on the skin outnumber human cells by at least 10 times (about 100 trillion microbial symbionts)

  • Microbial community composition is determined primarily by habitat (well, of course!)

  • The composition of microbial communities varies widely from one person to another

  • The compostion of microbial communities for an individual human do not vary much over time

  • Some locations of the skin harbor more diverse communities than even the mouth or gut
Want to know more?
Bacterial Community Variation in Human Body Habitats Across Space and Time.
Elizabeth K. Costello, et al. 
Science Express, 5 November 2009, online .
doi: 10.1126/science.1177486
[Recent study on human flora]

Bacteria Flourish in Favorite Ecosystems on the Human Body
Laura Sanders
Science News November 5, 2009
[Nice summary of the study's importance and implications]

Variation In Bacterial Populations From Person To Person Surprises Researchers

C. Paddock
Medical News Today 6 November 2009
[Press release about the new study]

Skin Ecology
K. Patton
The A&P Professor 18 November 2008
[My previous article on the topic.  Includes links to other articles.]

Why cells cooperate


Here's a nice little "animated clay" video that zeroes in on the "society of cells" concept that lies at the heart of homeostasis.   Because it goes on to emphasize the role of reproductive cells in a multicellular organism, it may be useful to help our A&P students connect reproduction to the concept of overall body homeostasis.

I saw this video on public radio's Science Friday website, where they have a weekly video recommendation.

The video comes from a collection of videos at creaturecast.org that are truly amazing.  Not very many directly relate to human anatomy and physiology . . . but, wow, they are fascinating.  For example, a recent posting discusses how mitochondria and other erstwhile endosymbionts can play a variety of roles such as acting as lenses for simple animals. I teach the serial endosymbiosis theory (SET)  in my A&P course . . . so this little factoid may help spice up that discussion.

So watch the FREE video about cell cooperation in a multicellular organism and let me know what you think!


H1N1 teaching moments


Although the typical A&P class is not focused primarily on pathology, we certainly do use pathology frequently as a tool to illustrate "normal" structure and function by looking at what goes wrong in injury and disease.  This works especially well when a disease or injury . . . or affected celebrity . . . is in the current news.  The current pandemic H1N1 outbreak gives us opportunities to teach some important concepts:
  • what do "public health" scientists do, and how do they do it?
  • what is a virus and how does it affect cell and body function?
  • how do vaccines protect the body?
  • why do some infections have a greater affect on some people than others?
  • how are viral infections spread?  how are they treated?
A recent news release posted at Science Daily summarizes a striking issue related to the flu vaccinations.  It highlights a paper recently published in The Lancet, which concludes that vaccination campaigns can be underminded by the public's tendency to link coincidental health events with vaccination campaigns.

Haven't we all see and heard of such associations?  They are even promoted by some otherwise trustworthy media outlets.  For example, many people are convinced of the strong relationship between certain vaccine preservatives and autism . . . even though thorough scientific investigation has shown no link.  An "outbreak" of Guillain–Barré Syndrome during the 1976-77 swine flu vaccination program turns out to be consistent with the number of people expected to contract this syndrome whether or not a vaccination program occurred.

In short, people get sick all the time and we should not automatically conclude that coincidental events are necessarily cause-and-effect scenarios . . . or even related at all.  And yet . . . we do.

This information is useful in teaching about how the scientific method can be used to answer questions.  In addition, the CDC's current surveillance methodology can be explored to illustrate how a scientific approach can be used in practical ways to watch for actual problems that could arise in a vaccination program.


In a somewhat related development, psychologists recently reported in Psychological Science that seeing and hearing a person sneeze can trigger fear or a "doom-and-gloom" attitude in healthy individuals.  I guess we should be cautious when exposed to sneezes, but the study showed that we tend to take such stimuli far more seriously than we realized.

Want to know more?
Pandemic Flu Vaccine Campaigns May Be Undermined By Coincidental Medical Events.
Cincinnati Children's Hospital Medical Center ScienceDaily. (2009, November 6)
[News release summarizing conclusions of a scientific study]

Importance of background rates of disease in assessment of vaccine safety during mass immunisation with pandemic H1N1 influenza vaccines
Black, S. et al.
The Lancet (early online publication) 31 October 2009
doi:10.1016/S0140-6736(09)61877-8
[Original peer-reviewed article]
Sneezes Provoke Fears Beyond Illness
Karen Hopkin
Sceintific American Online November 4, 2009
[Link to the podcast version or read the text summary]
[Here's an interesting clip to add to your PowerPoint or course web page . . . the first filmed sneeze ever recorded!  It was made with Thomas Edison's kinetoscope and was the first motion picture copyrighted in the United States.  Click here to see it http://bit.ly/j0Mzf ]

Monday, October 26, 2009

Revisiting the spleen


I'll never forget that snowy day all those years ago when my friend Keith slammed his sled into a laundry pole and ruptured his spleen.  Perhaps as an expression of our shock and concern for him as he lay in his hospital bed after his splenectomy, we spent an afternoon wondering to each other, "what IS a spleen . . . and how can you live without one?" 

As we all know, the spleen has a number of functions including acting as a blood reservoir and as a site of lymphocyte development and activity.  Research published a few months ago has now expanded our understanding of this odd organ.

According to the new research, another function of the spleen is to serve as a reservoir of monocytes that can be called upon during tissue injury in other locations of the body.  The splenic monocytes, which far outnumber the monocytes circulating in the bloodstream, form clusters in the cords of red pulp just under the capsule (wall of the organ).  From there, they move in a group out of the spleen and to the site of injury.  There they help remove and repair damaged tissue. 


This is a FREE image (click for source).
You can use it in your course.



Want to know more?
Identification of Splenic Reservoir Monocytes and Their Deployments to Inflammatory Sites
Swirski, F. K. et al.
Science 31 July 2009: Vol. 325, no. 5940, pp. 612-616
DOI: 10.1126/science.1175202
[The original research article.  A particularly clear abstract.]

Dispensible But Not Irrelevant
Jia T. et al.
Science 31 July 2009: Vol. 325. no. 5940, pp. 549 - 550
DOI: 10.1126/science.1178329

[Editor's summary of the implications of the original research.  Full text version includes a great diagram of this newly discovered role of the spleen.]

Finally, the Spleen Gets Some Respect
N. Angier
The New York Times 3 August 2009
[Article summarizing the new findings.]

While we're on the subject of the spleen, have you seen the images of a pelvic spleen published recently in the New England Journal of Medicine?  The piece in the NEJM briefly documents the case of a rare condition in which the spleen my drop into the pelvic cavity when there is problem with the suspensory ligaments of the spleen.

Pelvic Spleen: Images in Clinical Medicine
Tseng and Chou
New England Journal of Medicine 361 (13): 1291, Figure 1
[Images.  Includes link to FREE PowerPoint slide for subscribers]


 For a few FREE images of the spleen, go to the Lymphatic Image Library at The A&P Professor website

Keeping time


Finally . . . a physiological explanation for why I have such hard time keeping time when trying to dance.  Any of you who have seen me on the dance floor at a Human Anatomy and Physiology Society (HAPS) conference know what I mean!

It turns out that there are time-keeping neurons in our brains.  Specifically in the prefrontal cortex and striatum of the cerebrum. Discovered recently in the brains of monkeys by researchers at MIT, these time-keeping neurons fire consistently at certain rhythms . . . thus helping our brains to figure out when things are happening.  This helps us with rhythmic activities, of course, but also with any number of tasks and memories that rely on knowing what came first, in what order, and so on. 

Researchers speculate that damage to these neurons, or damage to the mechanisms that read the timing pattern, may contribute to disorders (such as Parkinson Disease) that involve ill-timed movements and other functions.  And perhaps may explain why Kevin has a such a hard time dancing.

In their paper, researchers failed to speculate whether this is why A&P students know exactly when to start slamming their books shut moments before a class is scheduled to end.

Want to know more?

Neural representation of time in cortico-basal ganglia circuits
Jin, DZ et al.
Proceedings of the National Academy of Sciences, 22 Oct 2009


[Original research article]




Time-keeping Brain Neurons Discovered

Massachusetts Institute of Technology (2009, October 23).
[Press release summarizing the context of the discovery.]

Monday, October 19, 2009

Why the Golgi apparatus looks so funny

Did you ever wonder why the Golgi apparatus looks so odd, compared to other membranous organelles of the cell?  I mean, really, wouldn't you think that the forces causing other membrane-bound structures to form more of a globular shape would cause the cisternae (sacs) of the Golgi apparatus to be more, well, round?

A few days ago, the journal Cell published an article that answers that question . . . revealing an elegant mechanism resulting from the primary function of the Golgi apparatus.

As we know, the Golgi apparatus "processes and packages" proteins that arrive from the endoplasmic reticulum (ER) by way of ER vesicles. The central structure of the organelles is the Golgi stack or dictyosome, which resembles a stack of hollow pancakes. Vesicles pinch off of the first cisterna (cis face) and move to the next cisterna, then the next, and finally to the final cisterna (trans face).  Then a vesicle pinches off and moves to the plasma membrane, where it fuses and releases (secretes) it contents to the outside of the cell (exocytosis).

The new data suggest that the budding of vesicles and their movement toward the plasma membrane rely on the function of a protein called GOLPH3.  This tiny protein connects special phospholipid molecules [PtdIns(4)P] in the Golgi membrane to myosin molecules (MYO18A).  The myosin, in turn, is attached to F-actin filaments of cytoskeleton.  Well, you know what that means, right?  Yes . . . the myosin is a motor molecule that pulls the attached Golgi membrane along the F-actin filament, stretching it out into its familiar elongated shape.  Then thwap! . . . a vesicle pinches off and is carried away.

In short, the Golgi membranes flatten out because they are being pulled outward by the cytoskeleton in a process that produces budding of vesicles.  As simple as that!  Now, when you're describing this amazing little organelle in your A&P class, you have a new little twist to add to the story! 


By the way, the terms Golgi complex and Golgi apparatus, which are synonyms, are among the rare eponyms that appear in the Terminologia Histologica (TH). As you recall, the TH is the "official" list of microscopic anatomy terms produced by the FIPAT (Federative International Programme on Anatomical Terminologies).  It is named for its discoverer Camillo Golgi, who was at first ridiculed for believing it to be a distinct organelle.

(For a video on international terminology that you can share with students, go to http://www.youtube.com/watch?v=94PU6J3Y9mA)

Now for the next question to be answered . . . what mechanism pulled Golgi's mustache out into that crazy handlebar shape?
 
GOLPH3 bridges phosphatidylinositol-4-phosphate and actomyosin to stretch and shape the golgi to promote budding. 
Dippold, H.C. et al. 
Cell 139 (Oct. 16) 2009. 
DOI 10.1016/j.cell.2009.07.052
[The original paper. The "supplemental material" icludes a video showing the stretching of the Golgi]

Golgi's Job Stretches it Thin
Lisa Grossman
Science News October 19, 2009
[Summary article explains the context and importance of the discovery]

[For more FREE images of the Golgi apparatus, visit the FREE Image Library at The A&P Professor website.]

Flu facts . . . the basics about H1N1

The CDC tells us that there is widespread 2009 novel H1N1 influenza activity in 41 states and that the number of cases, hospitalizations, and deaths continue to increase.
 
Many of you have begun implementing strategies on your campus to minimize the spread of the flu, including self-isolation of faculty, staff, and students with flu-like symptoms.  The CDC suggests that nearly all flu cases right now are 2009 novel H1N1 infections.

Recently, I published a brief article in a publication called The Global Pages on my home campus that lays out the basic science needed to understand what's going on.  It's not a detailed report of the current status or all the complicated virology and epidemiology involved.  It's just a basic foundation of essential terms and key concepts about viruses, public health management, and this particular flu strain.  And why it's not really "swine flu" in the strictest sense, anyway.  It's directed at the average student (not particularly science students).


I'm sharing it because it may help you answer those inevitable questions that your students may have.  Feel free to share it with your students.

Novel H1N1--A Global Health Threat
Kevin Patton
The Global Pages Vol. 10 (No. 1) Fall 2009 St. Charles Community College
[A PDF-format handout that you can read and/or share with your students.  Click here for a SWF-format file that you can embed in a PowerPoint slide or a course web page.] 
 

Action potential in action


I recently found a really nice FREE animation of the action potential. It's from Harvard's outreach program and it does a great job of breaking down the essential processes of this hard-to-learn, hard-to-teach concept.

I've just added it to my own course outline so that my students can access it easily. One might also use it during class, or a tutoring session with students, to reinforce understanding of the action potential's mechanisms. Hmmm . . . this could also be a good thing to go through with my students in my A&P 1 Supplement course, eh?
Action Potential Animation
[Interactive animation]

Action Potential Video
[Another nice, animated explanation of the action potential]

Action Potential Diagram
[A free diagram of the action potential. Compares the ideal "schematic" to a recorded action potential.]

Monday, October 12, 2009

Virtual autopsies


Wow, this goes on my wish list for the holiday season. Take a look at the Virtual Autopsy system at visualiseringscenter.se

After scanning a body, users can manipulate the images on what my editor, Jeff Downing, calls "an iPhone on steroids." It's a big table-top, touch-screen monitor that shows high-resolution 3D images of the scanned body.

The creators tout their project as a potential solution to situations where traditional autopsies cannot be performed (for example, in areas where cultural taboos prohibit it). It can also be a complement to traditional autopsies because it can show things that may not be visible during the routine type of examination.

Besides the gee-whiz, ain't that cool factor you'll experience when you check it out, you may want to consider showing one of the FREE video clips to your students to show them what's happening out there on the cutting edge of anatomy applications. This might be a great bit to add to your "first lecture" dog-and-pony show to get your students engaged and excited about human A&P.

There are also some cool case study ideas included at the demo page.

If you get one of these things, let me know. I want to come and play with it!

Visual Analogy Guides


Well, it's "book order" time here at my college and I'm going to be recommending a series of student supplements for A&P that I've found to be really, really helpful. The Visual Analogy Guide series has been used by my students for a couple of years now and my students love them.

Created by my friend Paul Krieger at Grand Rapids Community College (GRCC), the Visual Analogy Guides really meet the students where they are at to help them master some of those little tricks for learning the core concepts of an A&P course.

Using his considerable skills as an illustrator and his great talent as a teacher, Paul has put together some great tools that help students focus their study time by using visual and kinesthetic processes to help them learn "the hard parts" of A&P.

Check out his video
, in which he explains how the Visual Analogy Guides work.