Author
Listed:
- Zaman Mirzadeh
(Barrow Neurological Institute)
- Yael Kusne
(Barrow Neurological Institute)
- Maria Duran-Moreno
(Laboratory of Comparative Neurobiology, Instituto Cavanilles, CIBERNED, Universidad de Valencia)
- Elaine Cabrales
(Barrow Neurological Institute)
- Sara Gil-Perotin
(Laboratory of Comparative Neurobiology, Instituto Cavanilles, CIBERNED, Universidad de Valencia)
- Christian Ortiz
(Cell and Developmental Biology, University of California)
- Bin Chen
(Cell and Developmental Biology, University of California)
- Jose Manuel Garcia-Verdugo
(Laboratory of Comparative Neurobiology, Instituto Cavanilles, CIBERNED, Universidad de Valencia)
- Nader Sanai
(Barrow Neurological Institute)
- Arturo Alvarez-Buylla
(University of California)
Abstract
Multiciliated ependymal (E1) cells line the brain ventricles and are essential for brain homeostasis. We previously identified in the lateral ventricles a rare ependymal subpopulation (E2) with only two cilia and unique basal bodies. Here we show that E2 cells form a distinct biciliated epithelium extending along the ventral third into the fourth ventricle. In the third ventricle floor, apical profiles with only primary cilia define an additional uniciliated (E3) epithelium. E2 and E3 cells’ ultrastructure, marker expression and basal processes indicate that they correspond to subtypes of tanycytes. Using sonic hedgehog lineage tracing, we show that the third and fourth ventricle E2 and E3 epithelia originate from the anterior floor plate. E2 and E3 cells complete their differentiation 2–3 weeks after birth, suggesting a link to postnatal maturation. These data reveal discrete bands of E2 and E3 cells that may relay information from the CSF to underlying neural circuits along the ventral midline.
Suggested Citation
Zaman Mirzadeh & Yael Kusne & Maria Duran-Moreno & Elaine Cabrales & Sara Gil-Perotin & Christian Ortiz & Bin Chen & Jose Manuel Garcia-Verdugo & Nader Sanai & Arturo Alvarez-Buylla, 2017.
"Bi- and uniciliated ependymal cells define continuous floor-plate-derived tanycytic territories,"
Nature Communications, Nature, vol. 8(1), pages 1-12, April.
Handle:
RePEc:nat:natcom:v:8:y:2017:i:1:d:10.1038_ncomms13759
DOI: 10.1038/ncomms13759
Download full text from publisher
Corrections
All material on this site has been provided by the respective publishers and authors. You can help correct errors and omissions. When requesting a correction, please mention this item's handle: RePEc:nat:natcom:v:8:y:2017:i:1:d:10.1038_ncomms13759. See general information about how to correct material in RePEc.
If you have authored this item and are not yet registered with RePEc, we encourage you to do it here. This allows to link your profile to this item. It also allows you to accept potential citations to this item that we are uncertain about.
We have no bibliographic references for this item. You can help adding them by using this form .
If you know of missing items citing this one, you can help us creating those links by adding the relevant references in the same way as above, for each refering item. If you are a registered author of this item, you may also want to check the "citations" tab in your RePEc Author Service profile, as there may be some citations waiting for confirmation.
For technical questions regarding this item, or to correct its authors, title, abstract, bibliographic or download information, contact: Sonal Shukla or Springer Nature Abstracting and Indexing (email available below). General contact details of provider: http://www.nature.com .
Please note that corrections may take a couple of weeks to filter through
the various RePEc services.