Morshead C M, Reynolds B A, Craig C G, McBurney M W, Staines W A, Morassutti D, Weiss S, van der Kooy D
University of Toronto, Department of Anatomy and Cell Biology, Ontario, Canada.
Neuron. 1994 Nov;13(5):1071-82. doi: 10.1016/0896-6273(94)90046-9.
Dissection of the subependyma from the lateral ventricle of the adult mouse forebrain is necessary and sufficient for the in vitro formation of clonally derived spheres of cells that exhibit stem cell properties such as self-maintenance and the generation of a large number of progeny comprising the major cell types found in the central nervous system. Killing the constitutively proliferating cells of the subependyma in vivo has no effect on the number of stem cells isolated in vitro and induces a complete repopulation of the subependyma in vivo by relatively quiescent stem cells found within the subependyma. Depleting the relatively quiescent cell population within the subependyma in vivo results in a corresponding decrease in spheres formed in vitro and in the final number of constitutively proliferating cells in vivo, suggesting that a relatively quiescent subependymal cell is the in vivo source of neural stem cells.
从成年小鼠前脑侧脑室分离室管膜下区,对于体外形成具有干细胞特性(如自我维持以及产生大量包含中枢神经系统中主要细胞类型的子代细胞)的克隆衍生细胞球而言,是必要且充分的条件。在体内杀死室管膜下区持续增殖的细胞,对体外分离的干细胞数量没有影响,反而会促使室管膜下区中相对静止的干细胞在体内完全重新填充室管膜下区。在体内耗尽室管膜下区相对静止的细胞群,会导致体外形成的细胞球数量相应减少,以及体内持续增殖细胞的最终数量减少,这表明相对静止的室管膜下细胞是神经干细胞的体内来源。