Kohno Ri-ichiro, Ikeda Yasuhiro, Yonemitsu Yoshikazu, Hisatomi Toshio, Yamaguchi Masahiro, Miyazaki Masanori, Takeshita Hiroko, Ishibashi Tatsuro, Sueishi Katsuo
Division of Pathophysiological and Experimental Pathology, Department of Pathology, Graduate School of Medical Sciences, Kyushu University, 3-1-1 Maidashi, Higashi-ku, Fukuoka 812-8582, Japan.
Brain Res. 2006 Jun 6;1093(1):54-70. doi: 10.1016/j.brainres.2006.03.093. Epub 2006 May 11.
It is well known that neural stem/progenitor cells of the central nervous system (CNS) can proliferate to form neurospheres (CNS-neurospheres) that are positive for nestin, an intermediate filament for neural progenitors. Retinal stem/progenitor properties were also isolated from the ciliary body (CB) of the eye where, as in the CNS, such stem/progenitors also form spheres and have been considered to expand only via expansion by their proliferation even from the single-cell level (called spheres of pigment cells from the ciliary margin: PCM-spheres). We here found a new and distinct process underlying the growth of CB cell-derived spheres (CB-spheres) that is unlike the mechanism of CNS- and PCM-sphere expansion; this new process is a cell proliferation-independent incorporation of neighbor spheres and cells cultured at high density (200 cells/mul). The majority of cells in CB-spheres consisted of nestin-negative epithelia-like cells and started to express nestin during the course of their expansion by high-density cultivation. The growth of CNS-neurospheres was sensitive to a cell-cycle inhibitor, whereas the growth of CB-spheres was not seriously affected by cell proliferation; rather, the spheres grew by incorporating other CB-spheres and nestin-negative adherent cells, the latter of which started to express nestin and lost the expression of epithelial markers after being incorporated. These results indicate that CB-spheres do not form by the accumulation of neural progenitors but rather by a reprogramming system from epithelia-like cells for neural differentiation, a clearly distinct mechanism from sphere formation by single-cell expansion of retinal stem/progenitor populations.
众所周知,中枢神经系统(CNS)的神经干细胞/祖细胞能够增殖形成对巢蛋白呈阳性的神经球(CNS-神经球),巢蛋白是神经祖细胞的一种中间丝。视网膜干细胞/祖细胞特性也从眼睛的睫状体(CB)中分离出来,在那里,与中枢神经系统一样,这种干细胞/祖细胞也形成球体,并且即使从单细胞水平开始也被认为仅通过增殖来扩大(称为来自睫状缘的色素细胞球体:PCM-球体)。我们在此发现了一种不同于中枢神经系统和PCM-球体扩张机制的、独特的CB细胞衍生球体(CB-球体)生长新过程;这个新过程是一种不依赖细胞增殖的、对高密度培养(200个细胞/微升)的相邻球体和细胞的合并。CB-球体中的大多数细胞由巢蛋白阴性的上皮样细胞组成,并在通过高密度培养进行扩张的过程中开始表达巢蛋白。CNS-神经球的生长对细胞周期抑制剂敏感,而CB-球体的生长不受细胞增殖的严重影响;相反,球体通过合并其他CB-球体和巢蛋白阴性的贴壁细胞而生长,后者在被合并后开始表达巢蛋白并失去上皮标志物的表达。这些结果表明,CB-球体不是由神经祖细胞的积累形成的,而是由上皮样细胞重编程为神经分化的系统形成的,这是一种与视网膜干细胞/祖细胞群体单细胞扩张形成球体的机制明显不同的机制。