4.7 Article

Regulation of neural progenitor cell state by ephrin-B

期刊

JOURNAL OF CELL BIOLOGY
卷 181, 期 6, 页码 973-983

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ROCKEFELLER UNIV PRESS
DOI: 10.1083/jcb.200708091

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资金

  1. NICHD NIH HHS [HD25326, R01 HD025326, R37 HD025326] Funding Source: Medline
  2. NINDS NIH HHS [R01 NS052388, NS52388] Funding Source: Medline

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Maintaining a balance between self-renewal and differentiation in neural progenitor cells during development is important to ensure that correct numbers of neural cells are generated. We report that the ephrin-B-PDZ-RGS3 signaling pathway functions to regulate this balance in the developing mammalian cerebral cortex. During cortical neurogenesis, expression of ephrin-B1 and PDZ-RGS3 is specifically seen in progenitor cells and is turned off at the onset of neuronal differentiation. Persistent expression of ephrin-B1 and PDZ-RGS3 prevents differentiation of neural progenitor cells. Blocking RGS-mediated ephrin-B1 signaling in progenitor cells through RNA interference or expression of dominant-negative mutants results in differentiation. Genetic knockout of ephrin-B1 causes early cell cycle exit and leads to a concomitant loss of neural progenitor cells. Our results indicate that ephrin-B function is critical for the maintenance of the neural progenitor cell state and that this role of ephrin-B is mediated by PDZ-RGS3, likely via interacting with the noncanonical G protein signaling pathway, which is essential in neural progenitor asymmetrical cell division.

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