A novel role for Gab2 in bFGF-mediated cell survival during retinoic acid-induced neuronal differentiation

Yingwei Mao, Angel W.M. Lee

Research output: Contribution to journalArticle

39 Scopus citations

Abstract

Gab proteins amplify and integrate signals stimulated by many growth factors. In culture and animals, retinoic acid (RA) induces neuronal differentiation. We show that Gab2 expression is detected in neurons in three models of neuronal differentiation: embryonic carcinoma (EC) stem cells, embryonic stem cells, and primary neural stem cells (NSCs). RA treatment induces apoptosis, countered by basic FGF (bFGF). In EC cells, Gab2 silencing results in hypersensitivity to RA-induced apoptosis and abrogates the protection by bFGF. Gab2 suppression reduces bFGF-dependent G activation of AKT but not ERK, and constitutively active AKT, but not constitutively active MEK1, reverses the hypersensitization. Thus, Gab2-mediated AKT activation is required for bFGF's protection. Moreover, Gab2 silencing impairs the differentiation of EC cells to neurons. Similarly, in NSCs, Gab2 suppression reduces bFGF-dependent proliferation as well as neuronal survival and production upon differentiation. Our findings provide the first evidence that Gab2 is an important player in neural differentiation, partly by acting downstream of bFGF to mediate survival through phosphoinositide 3 kinase-AKT.

Original languageEnglish (US)
Pages (from-to)305-316
Number of pages12
JournalJournal of Cell Biology
Volume170
Issue number2
DOIs
Publication statusPublished - Jul 1 2005

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All Science Journal Classification (ASJC) codes

  • Cell Biology

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