Kerever Aurelien, Mercier Frederic, Nonaka Risa, de Vega Susana, Oda Yuka, Zalc Bernard, Okada Yohei, Hattori Nobutaka, Yamada Yoshihiko, Arikawa-Hirasawa Eri
Research Institute for Diseases of Old Age, Juntendo University Graduate School of Medicine, Tokyo, Japan.
Department of Tropical Medicine and Infectious Diseases, John A. Burns School of Medicine, University of Hawaii, Honolulu, HI, USA.
Stem Cell Res. 2014 Mar;12(2):492-505. doi: 10.1016/j.scr.2013.12.009. Epub 2013 Dec 28.
In the adult subventricular zone (neurogenic niche), neural stem cells double-positive for two markers of subsets of neural stem cells in the adult central nervous system, glial fibrillary acidic protein and CD133, lie in proximity to fractones and to blood vessel basement membranes, which contain the heparan sulfate proteoglycan perlecan. Here, we demonstrate that perlecan deficiency reduces the number of both GFAP/CD133-positive neural stem cells in the subventricular zone and new neurons integrating into the olfactory bulb. We also show that FGF-2 treatment induces the expression of cyclin D2 through the activation of the Akt and Erk1/2 pathways and promotes neurosphere formation in vitro. However, in the absence of perlecan, FGF-2 fails to promote neurosphere formation. These results suggest that perlecan is a component of the neurogenic niche that regulates FGF-2 signaling and acts by promoting neural stem cell self-renewal and neurogenesis.
在成体脑室下区(神经发生微环境),神经干细胞对成体中枢神经系统神经干细胞亚群的两种标志物呈双阳性,即胶质纤维酸性蛋白和CD133,它们位于纤维束和血管基底膜附近,血管基底膜含有硫酸乙酰肝素蛋白聚糖多配体蛋白。在此,我们证明多配体蛋白缺乏会减少脑室下区GFAP/CD133阳性神经干细胞以及整合到嗅球中的新神经元的数量。我们还表明,FGF-2处理通过激活Akt和Erk1/2信号通路诱导细胞周期蛋白D2的表达,并在体外促进神经球形成。然而,在缺乏多配体蛋白的情况下,FGF-2无法促进神经球形成。这些结果表明,多配体蛋白是神经发生微环境的一个组成部分,它调节FGF-2信号传导,并通过促进神经干细胞自我更新和神经发生发挥作用。