Dissecting integrin-dependent regulation of neural stem cell proliferation in the adult brain

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Abstract

Controlling neural stem and progenitor cell (NSPC) proliferation is critical to maintain neurogenesis in the mammalian brain throughout life. However, it remains poorly understood how niche-derived cues such as β1-integrin-mediated signaling are translated into NSPCintrinsic molecular changes to regulate NSPC activity. Here we show that genetic deletion of integrin-linked kinase (ILK) increases NSPC proliferation through PINCH1/2-dependent enhancement of c-Jun N-terminal protein kinase activity in both neurogenic regions of the adult mouse brain. This effect downstream of ILK signaling is mediated through loss of Ras suppressor unit-1 (RSU-1), as virus-based reconstitution of RSU-1 expression rescued the ILK-dependent effects on NSPC proliferation. Thus, we here identified an intracellular signaling cascade linking extrinsic integrin-mediated signaling to NSPC proliferation and characterized a novel mechanism that regulates NSPC activity in the adult mammalian brain. © 2014 the authors.

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Porcheri, C., Suter, U., & Jessberger, S. (2014). Dissecting integrin-dependent regulation of neural stem cell proliferation in the adult brain. Journal of Neuroscience, 34(15), 5222–5232. https://doi.org/10.1523/JNEUROSCI.4928-13.2014

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