Wrap your brain around precursor cells

Posted by on February 10th, 2012

A fully differentiated cell took a fascinating journey to become its present self.  For every cell, a precursor cell existed that gave rise to it.  And for every precursor cell, a stem cell existed that gave rise to it.  Understanding precursor cells is an important part in understanding stem cell biology.  Today’s image is from a recent paper in Development that discusses how neuron precursor cell divisions affect development of the cerebral cortex.

The cerebral cortex is the outermost layer or brain tissue, and is commonly referred to as “gray matter.”  During development, the different regions and layers of the cerebral cortex are formed from precursor cells.  These intermediate precursor cells (IPCs) arise from radial glial cells (RGCs), which come from neural stem cells. The different layers of the cortex are formed from radial migration of the postmitotic neurons produced by RGCs and IPCs.  The length of time each RGC or IPC cell resides in the cell cycle regulates the distance its daughter neuron can migrate—cells that exit the cell cycle earlier are able to migrate further, while neurons that are born later cannot migrate as far.  Exploring this connection between the cell cycle and formation of cortex layers, Mairet-Coello and colleagues recently published results showing how two different cyclin-dependent kinase inhibitors (CKIs) regulate different stages of precursor proliferation and affects development of the different layers.  Specifically, p57KIP2 regulates the cell cycle length of RGCs and IPCs, which in turn affects neurogenesis of layers 5 and 6.  p27KIP1, however, regulates the proliferation of IPCs, in turn affecting neurogenesis exclusively in layers 2-5.  In the images above, p57KIP2(red) is found in actively dividing precursor cells (PCNA, green) in two different proliferative zones in the developing mouse brain, labeled SV and SVZ.  The SV contains proliferating RGCs and IPCs, while the SVZ mostly contains proliferating IPCs.  Arrows point to p57KIP2-postitive proliferating cells.

For a more general description of this image, see my imaging blog within EuroStemCell, the European stem cell portal.

ResearchBlogging.org

Mairet-Coello, G., Tury, A., Van Buskirk, E., Robinson, K., Genestine, M., & DiCicco-Bloom, E. (2012). p57KIP2 regulates radial glia and intermediate precursor cell cycle dynamics and lower layer neurogenesis in developing cerebral cortex Development, 139 (3), 475-487 DOI: 10.1242/dev.067314
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This is what a scientist looks like

Posted by on February 8th, 2012

What do you look like? The website This Is What A Scientist Looks Like wants to know. The site, run by science writer Allie Wilkinson, is collecting photos of scientists to show people what we look like. It’s an attempt to combat the very stereotypical view of scientists many people have. Just do a Google Image search for the word “scientist”, and you’ll find many messy-haired men in white lab coats. While some scientists may indeed look like the stereotype, most others don’t! This Is What A Scientist Looks Like shows that scientists come in all shapes and sizes, have hobbies and families, and look like everyone else:



(If you’d like to submit your own photo to the project, submission info is on the site.)


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SDB Collaborative Resources (CoRe) Launched

Posted by on January 27th, 2012

The Society for Developmental Biology (SDB) has launched SDB Collaborative Resources (CoRe), an online collection of images, movies, and diagrams for learning and teaching developmental biology.  SDB CoRe is a free and open website developed to help increase understanding of developmental biology at all levels.




SDB CoRe is easily-searchable and can be browsed by topic, organism, or featured objects.  All objects have short descriptions aimed at helping users learn something about development with glossary words highlighted in green.  Object pages contain references as well as  links to related CoRe objects, links to reviews in the soon-to-be-launched WIREs Developmental Biology, and when relevant, to original research papers in SDB’s official journal Developmental Biology.  All users can create a My CoRe account in order to comment on an object or save it in their favorites.


SDB needs your help in building this community resource!  We are looking for visuals that help explain basic concepts in developmental biology across numerous plant and animal species.  Here are the guidelines for submitting to CoRe.  If you are an SDB member you can login to CoRe with your email address to submit.  Non-members that would like to submit to CoRe please contact me at info@sdbcore.org.  If you have any questions or suggestions for the site please email me as well.  Enjoy SDB CoRe!
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Shaggy hairs and stem cells

Posted by on January 10th, 2012

Our intestinal tissue doesn’t need a New Year’s resolution to keep up its amazing productivity.  Our intestinal epithelium is replenished at breakneck speed in an assembly line that begins with stem cells.  Today’s image is from a recent Development paper that discusses the importance of Notch signaling in stem cell self-renewal and intestinal homeostasis.



Our intestinal epithelium is folded and shaped into finger-like villi (“shaggy hair” in Latin) that increase the surface area of the tissue for more nutrient absorption.  Each villus has several populations of cells in homeostasis in order to maintain function and constant replenishment.  This production of epithelium starts with the actively-dividing crypt base columnar (CBC) stem cells that sit in the crypts.  Although the identity of these cells has been known for a while, the factors regulating CBC stem cell self-renewal and differentiation were not well understood.  A recent Development paper discusses the role for Notch signaling in CBC stem cell function.  According to VanDussen and colleagues, Notch signaling is required for CBC stem cell self-renewal and survival.  Notch inhibition caused a decrease in the number CBC cells, as well as precocious differentiation of more specialized intestinal cell types.  VanDussen and colleagues showed that Notch regulates CBC cell self-renewal and cell fate choice through different pathways and by targeting different cell populations.  In the images above, intestinal tissue was stained for a marker of CBC stem cells (Lgr5, green) and for proliferating cells (Ki67, red).  In normal tissue (left), CBC stem cells were found at the base of the crypts, some of which were also actively dividing (arrows).  Notch inhibition (right) resulted in a misshapen morphology of CBC stem cells, a decrease in the CBC cell marker, and a drop in the number of CBC cells that were actively dividing (arrowheads on left).

For a more general description of this image, see my imaging blog within EuroStemCell, the European stem cell portal.

ResearchBlogging.orgVanDussen, K., Carulli, A., Keeley, T., Patel, S., Puthoff, B., Magness, S., Tran, I., Maillard, I., Siebel, C., Kolterud, A., Grosse, A., Gumucio, D., Ernst, S., Tsai, Y., Dempsey, P., & Samuelson, L. (2011). Notch signaling modulates proliferation and differentiation of intestinal crypt base columnar stem cells Development, 139 (3), 488-497 DOI: 10.1242/dev.070763
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Celestial or Cellular?

Posted by on December 26th, 2011

The Cell: An Image Library™ offers you a little fun this week. Please enjoy our quiz, Celestial or Cellular?
Take a look at the images and see if you can tell whether they are of cellular or celestial origin.
Take your best shot, and enter your answers at http://asterisk.apod.com/viewtopic.php?f=29&t=26228. Visit again each day this week for a new quiz and the correct answers to the previous day’s quiz.
Enjoy, and please share this with your friends.
Visit The Cell: An Image Library and learn how to submit your images.
Reuse of quiz images may be subject to licensing restrictions, which will be revealed with the identity of the image on the day following the quiz.
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Repulsive signals: bad breath, rude manners, and ephrin ligands

Posted by on December 7th, 2011

Satellite cells are muscle stem cells that regenerate injured muscle (remember this earlier post?).  They are highly motile cells that may be able to travel in order to repair injured muscle far away, and a recent paper in Development describes the role of Eph/ephrin signaling in satellite cell motility and patterning.


One of the most well-understood guidance pathways is the Eph/ephrin pathway, which has major roles in cell migration and axon guidance throughout development.  In this pathway, Eph receptors on one cell interact with ephrin ligands bound to another cell’s membrane.  This interaction typically causes rapid changes in the Eph-expressing cell’s adhesion and cytoskeletal organization, and frequently causes the cells to repel each other.  A recent paper describes the role of Eph/ephrin signaling in satellite cell motility and patterning.  Stark and colleagues showed that ephrin ligands are differentially localized to healthy and regenerating muscle tissue, and used a well-established “stripe assay” to show that ephrins can repel mouse satellite cells.  As seen in the images above (increasing magnification from left to right), stripes of ephrin-B1 ligand (bottom row, blue stripes) repulsed the satellite cells, compared to the distribution of cells on control stripes (top row).  In addition, Stark and colleagues explanted mouse satellite cells into the hindbrain of developing quail embryos, from which neural crest cells emigrate using Eph/ephrin signaling.  Some satellite cells migrated along with the neural crest cells and conformed to the same boundaries.

For a more general description of this image, see my imaging blog within EuroStemCell, the European stem cell portal.

ResearchBlogging.orgStark, D., Karvas, R., Siegel, A., & Cornelison, D. (2011). Eph/ephrin interactions modulate muscle satellite cell motility and patterning Development, 138 (24), 5279-5289 DOI: 10.1242/dev.068411
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December desktop calendar

Posted by on November 29th, 2011

And here it is: the last of the desktop wallpaper calendars. In June we celebrated our first birthday, and decided to give all our readers a virtual gift. It ended up being six gifts: one desktop calendar wallpaper for each remaining month of 2011. If you want to see all the images, or download the latest one, visit the calendar page. All images were chosen from either the intersection image contest or from the images we’ve featured from the Woods Hole Embryology 2010 course.

december_thumbnailOn the december calendar wallpaper, a dorsal view of the central nervous system of a Drosophila embryo.
This image, taken by Joshua Clanton of Vanderbilt University, was one of the candidates in the third Development cover image voting round of images taken at the 2010 Woods Hole Embryology course.

Visit the calendar page to select the resolution you need for your screen.
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Hair follicle stem cells – the hairy truth

Posted by on November 10th, 2011



Next time you curse your hair for your bad hair day, consider thanking it instead.  The hair follicle has populations of stem cells that aid in skin regeneration after injury, and a recent Development paper unravels a new role for the transcription factor Lhx2 in this process.

Populations of epithelial stem cells in hair follicles serve to rebuild the hair bulb during the normal hair cycle throughout our lives, but they also can migrate to wounded skin in order to aid in skin regeneration.   This ability is quite handy—when the skin in a hairy area is injured, it heals faster and more efficiently than a wound on skin without hair.  Recently, a research group illuminated the importance of the transcription factor Lhx2 in the repair of injured skin by hair follicle stem cells.  Lhx2 functions in organ development, cell fate determination, and stem cell activity in some organs.  In hair follicles, Lhx2 was previously known to regulate the switch between stem cell maintenance and activity.  In their recent report, Mardaryev and colleagues found that Lhx2+ hair follicle cells co-express several stem cell markers.  Following injury, proliferating cells in the adjacent hair follicle were positive for Lhx2 expression, as seen in the images above.  Lhx2 (magenta) expression increases by days 3 and 5 following injury.  Most of the dividing cells (green) also are Lhx2+.  In addition, cell proliferation following injury was reduced in heterozygous Lhx2 knockout (+/–) mice.   Lhx2 ensures wound re-epithelization through its regulation of Sox9 and Tcf4, while at the same time inhibiting normal hair follicle cycling via Lgr5 regulation.

For a more general description of this image, see my imaging blog within EuroStemCell, the European stem cell portal.

 
ResearchBlogging.orgMardaryev, A., Meier, N., Poterlowicz, K., Sharov, A., Sharova, T., Ahmed, M., Rapisarda, V., Lewis, C., Fessing, M., Ruenger, T., Bhawan, J., Werner, S., Paus, R., & Botchkarev, V. (2011). Lhx2 differentially regulates Sox9, Tcf4 and Lgr5 in hair follicle stem cells to promote epidermal regeneration after injury Development, 138 (22), 4843-4852 DOI: 10.1242/dev.070284
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November desktop calendar

Posted by on October 28th, 2011

It’s that time of the month again, when we upload the desktop calendar for next month. This time an image that you may remember from April - either from the contest on the Node or from the pub quiz at the BSDB meeting.

november_thumbnailIt’s a sea biscuit during metamorphosis from larval to adult stage. This image, taken by Bruno Vellutini of the Marine Biology Center of University of São Paulo, was the runner up in the Intersection Image Competition held earlier this year.

Visit the calendar page to select the resolution you need for your screen. The page will be updated at the end of each month with a new image, and all images are chosen from either the intersection image contest or from the images we’ve featured from the Woods Hole Embryology 2010 course.
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Aging stem cells

Posted by on October 12th, 2011

There are so many factors for a stem cell to consider when deciding cell fates.  A recent paper from Development discusses how the age of a stem cell can affect its future.



Neurons and glial cells are two major cell types in the nervous system, and both come from the many divisions of neural stem cells (NSCs).  The amazing plastic characteristics of NSCs drive a lot of excitement over their future use in regenerative medicine, but the complex gene network in vertebrates makes understanding NSC plasticity difficult.  Flici and colleagues recently published a paper on NSC cell fate decision-making in the simple CNS of fruit flies.  The transcription factor Gcm was already known to drive glial fate in NSCs.  Flici and colleagues found that overexpression of Gcm in NSCs forced a complete conversion to glial cells.  In addition, NSCs plasticity is affected by age—as NSCs get older, their ability to drive glial cell fates decreases.  After NCSs fell into a quiescent state at old age, Gcm overexpression was no longer able to force glial cell conversion, suggesting that temporal cues, not mitotic potential, drive NSC plasticity.  Finally, Flici and colleagues found that the Gcm-glial cell fate pathway leads to low levels of H3K9ac, which is similar to the low levels of histone acetylation seen in vertebrate glial cells.  In the images above, fly embryos are labeled to show neurons (green) and glial cells (purple).  Control embryos (left) have few glial cells, while embryos with Gcm overexpression (right) have many glial cells.  The longer the Gcm overexpression, the more glial cells develop at the expense of neurons (top is early, bottom is late).  Arrowheads show cells with markers for both glial cells and neurons, an intermediate stage in the conversion towards glial fate.

For a more general description of this image, see my imaging blog within EuroStemCell, the European stem cell portal.

ResearchBlogging.org

Flici, H., Erkosar, B., Komonyi, O., Karatas, O., Laneve, P., & Giangrande, A. (2011). Gcm/Glide-dependent conversion into glia depends on neural stem cell age, but not on division, triggering a chromatin signature that is conserved in vertebrate glia Development, 138 (19), 4167-4178 DOI: 10.1242/dev.070391

 
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