Ma Liping, Yin Min, Wu Xuefei, Wu Chunhua, Yang Shuo, Sheng Jiansong, Ni Hengjian, Fukuda Michiko N, Zhou Jiawei
Institute of Biochemistry and Cell Biology, Shanghai Institute for Biological Sciences, Shanghai, 200031, China.
Eur J Neurosci. 2006 May;23(9):2265-76. doi: 10.1111/j.1460-9568.2006.04782.x.
In the adult brain, the subventricular zone (SVZ) is one of the regions where active neurogenesis occurs. Relatively few specific markers are available to distinguish different types of cells in the SVZ and rostral migratory stream (RMS) of adult brain. Here, we showed that trophinin and bystin, both of which are required for early embryo implantation during development, were expressed in the SVZ and RMS of the adult rat brain, but not in the brain of embryos and early postnatal animals. Trophinin-expressing cells were immunopositive for both Ki-67 and nestin in the SVZ. Some of the trophinin-positive cells did not express either the type A cell marker polysialylated weakly adhesive form of the neural cell adhesion molecule (PSA-NCAM) or the type B cell marker glial fibrillary acidic protein (GFAP). Double-label immunohistochemistry revealed that bystin-positive cells co-expressed GFAP, Ki-67 and nestin, but not PSA-NCAM, suggesting that they are likely type B cells. Intracerebroventricular infusion of cytosine-beta-d-arabiofuranoside (Ara-C) eliminated trophinin-positive cells in the SVZ. Following its depletion, however, the remaining bystin-positive cells continued to divide and generate actively dividing trophinin-positive cells that were negative for PSA-NCAM, leading to reconstruction of SVZ network. These characteristics indicate that this subset of trophinin-positive cells in the SVZ is type C cells. Conversely in the RMS, trophinin co-localized with nestin and PSA-NCAM, suggesting that it is expressed in neuroblasts. Cultured neural precursor cells derived from the adult SVZ also expressed both trophinin and bystin. These findings provide insight into the molecular basis of adult neurogenesis in the SVZ and RMS.
在成人大脑中,脑室下区(SVZ)是发生活跃神经发生的区域之一。相对较少的特异性标志物可用于区分成人大脑SVZ和吻侧迁移流(RMS)中的不同类型细胞。在此,我们发现,在发育过程中早期胚胎着床所必需的促受精素和胚泡附着蛋白,在成年大鼠脑的SVZ和RMS中表达,但在胚胎脑和出生后早期动物的脑中不表达。在SVZ中,表达促受精素的细胞对Ki-67和巢蛋白均呈免疫阳性。一些促受精素阳性细胞既不表达A型细胞标志物神经细胞黏附分子的多唾液酸化弱黏附形式(PSA-NCAM),也不表达B型细胞标志物胶质纤维酸性蛋白(GFAP)。双重标记免疫组织化学显示,胚泡附着蛋白阳性细胞共表达GFAP、Ki-67和巢蛋白,但不表达PSA-NCAM,提示它们可能是B型细胞。脑室内注入β-D-阿拉伯呋喃糖胞苷(Ara-C)可消除SVZ中的促受精素阳性细胞。然而,在其耗竭后,剩余的胚泡附着蛋白阳性细胞继续分裂,并产生对PSA-NCAM呈阴性的活跃分裂促受精素阳性细胞,从而导致SVZ网络的重建。这些特征表明,SVZ中这一促受精素阳性细胞亚群是C型细胞。相反,在RMS中,促受精素与巢蛋白和PSA-NCAM共定位,提示它在神经母细胞中表达。源自成年SVZ的培养神经前体细胞也表达促受精素和胚泡附着蛋白。这些发现为SVZ和RMS中成年神经发生的分子基础提供了见解。