Skip to main content
. 2012 Oct 5;31(21):4103–4105. doi: 10.1038/emboj.2012.281

Figure 1.

Figure 1

Molecular model integrating both niche/environmental and cell autonomous theories of stem cell aging. Left: low level of niche-derived FGF2 permits spry1-dependent stem cell quiescence. Right: age-induced high FGF2 causes downregulation of spry1, which in turn leads to a cell autonomous alteration in the functionality of satellite cells and ultimately translates into stem cell decline.