Heterogeneity of Radial Glia‐Like Cells in the Adult Hippocampus. (4th January 2016)
- Record Type:
- Journal Article
- Title:
- Heterogeneity of Radial Glia‐Like Cells in the Adult Hippocampus. (4th January 2016)
- Main Title:
- Heterogeneity of Radial Glia‐Like Cells in the Adult Hippocampus
- Authors:
- Gebara, Elias
Bonaguidi, Michael Anthony
Beckervordersandforth, Ruth
Sultan, Sébastien
Udry, Florian
Gijs, Pieter‐Jan
Lie, Dieter Chichung
Ming, Guo‐Li
Song, Hongjun
Toni, Nicolas - Abstract:
- Abstract: Adult neurogenesis is tightly regulated by the neurogenic niche. Cellular contacts between niche cells and neural stem cells are hypothesized to regulate stem cell proliferation or lineage choice. However, the structure of adult neural stem cells and the contact they form with niche cells are poorly described. Here, we characterized the morphology of radial glia‐like (RGL) cells, their molecular identity, proliferative activity, and fate determination in the adult mouse hippocampus. We found the coexistence of two morphotypes of cells with prototypical morphological characteristics of RGL stem cells: Type α cells, which represented 76% of all RGL cells, displayed a long primary process modestly branching into the molecular layer and type β cells, which represented 24% of all RGL cells, with a shorter radial process highly branching into the outer granule cell layer‐inner molecular layer border. Stem cell markers were expressed in type α cells and coexpressed with astrocytic markers in type β cells. Consistently, in vivo lineage tracing indicated that type α cells can give rise to neurons, astrocytes, and type β cells, whereas type β cells do not proliferate. Our results reveal that the adult subgranular zone of the dentate gyrus harbors two functionally different RGL cells, which can be distinguished by simple morphological criteria, supporting a morphofunctional role of their thin cellular processes. Type β cells may represent an intermediate state in theAbstract: Adult neurogenesis is tightly regulated by the neurogenic niche. Cellular contacts between niche cells and neural stem cells are hypothesized to regulate stem cell proliferation or lineage choice. However, the structure of adult neural stem cells and the contact they form with niche cells are poorly described. Here, we characterized the morphology of radial glia‐like (RGL) cells, their molecular identity, proliferative activity, and fate determination in the adult mouse hippocampus. We found the coexistence of two morphotypes of cells with prototypical morphological characteristics of RGL stem cells: Type α cells, which represented 76% of all RGL cells, displayed a long primary process modestly branching into the molecular layer and type β cells, which represented 24% of all RGL cells, with a shorter radial process highly branching into the outer granule cell layer‐inner molecular layer border. Stem cell markers were expressed in type α cells and coexpressed with astrocytic markers in type β cells. Consistently, in vivo lineage tracing indicated that type α cells can give rise to neurons, astrocytes, and type β cells, whereas type β cells do not proliferate. Our results reveal that the adult subgranular zone of the dentate gyrus harbors two functionally different RGL cells, which can be distinguished by simple morphological criteria, supporting a morphofunctional role of their thin cellular processes. Type β cells may represent an intermediate state in the transformation of type α, RGL stem cells, into astrocytes. Stem Cells 2016;34:997–1010 Abstract : Model of the lineage relationship of type α and type β cells in the adult mouse hippocampus under basal conditions. Type α cells can self‐renew (1) and also generate type 2 neural progenitors (2), type β cells (3) and astrocytes (4). Type β cells do not divide, but may revert to type α cell (??) or transform into astrocytes (5). Also shown are marker expression. … (more)
- Is Part Of:
- Stem cells. Volume 34:Number 4(2016:Apr.)
- Journal:
- Stem cells
- Issue:
- Volume 34:Number 4(2016:Apr.)
- Issue Display:
- Volume 34, Issue 4 (2016)
- Year:
- 2016
- Volume:
- 34
- Issue:
- 4
- Issue Sort Value:
- 2016-0034-0004-0000
- Page Start:
- 997
- Page End:
- 1010
- Publication Date:
- 2016-01-04
- Subjects:
- Adult stem cells -- Nervous system -- Neural stem cell -- Somatic stem cells -- Stem cell‐microenvironment interactions
Cloning -- Periodicals
Clone cells -- Periodicals
Stem cells -- Periodicals
Cell Differentiation -- Periodicals
Cell Division -- Periodicals
Clone Cells -- Periodicals
Hematopoietic Stem Cells -- Periodicals
Stem Cells -- Periodicals
571.84 - Journal URLs:
- https://academic.oup.com/stmcls ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/stem.2266 ↗
- Languages:
- English
- ISSNs:
- 1066-5099
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 8464.133510
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 563.xml