Retinoic acid is required early during adult neurogenesis in the dentate gyrus

Sharoni Jacobs, D. Chichung Lie, Kathleen L. DeCicco, Yanhong Shi, Luigi M. DeLuca, Fred H. Gage, Ronald M. Evans

Research output: Contribution to journalArticlepeer-review

196 Scopus citations


Retinoic acid (RA) is commonly used in vitro to differentiate stem cell populations including adult neural stem cells into neurons; however, the in vivo function of RA during adult neurogenesis remains largely unexplored. We found that depletion of RA in adult mice leads to significantly decreased neuronal differentiation within the granular cell layer of the dentate gyrus. RA contribution to neurogenesis occurs early, for RA deficiency also results in a decrease in newborn cells expressing an immature neuronal marker. Furthermore, although proliferation is unaffected during RA absence, cell survival is significantly reduced. Finally, a screen for retinoid-induced genes identifies metabolic targets including the lipid transporters, CD-36 and ABCA-1, the lipogenic master regulator SREBP1c as well as components of the Wnt signaling pathway. Our results reveal RA as a crucial contributor to early stages of adult neurogenesis and survival in vivo.

Original languageEnglish (US)
Pages (from-to)3902-3907
Number of pages6
JournalProceedings of the National Academy of Sciences of the United States of America
Issue number10
StatePublished - Mar 7 2006
Externally publishedYes


  • Hippocampus
  • Neural stem cells
  • Retinoic acid receptor
  • Vitamin A

ASJC Scopus subject areas

  • General


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