Carletti Barbara, Rossi Ferdinando
Department of Neuroscience and Rita Levi Montalcini Centre for Brain Repair, University of Turin, Corso Raffaello 30, I-10125 Turin, Italy.
Eur J Neurosci. 2005 Sep;22(5):1001-12. doi: 10.1111/j.1460-9568.2005.04314.x.
Cell replacement after neuronal degeneration in the adult CNS depends on the availability of specific cues to direct specification, differentiation and integration of newly born neurons into mature circuits. Following recent reports indicating that neurogenic signals may be reactivated in the adult injured CNS, here we asked whether such signals are expressed in the cerebellum after Purkinje cell degeneration. Thus, we compared the fate of embryonic cerebellar cells transplanted to the cerebella of adult wild-type and Purkinje cell degeneration (pcd) mutant mice. Donor cells were dissected from beta-actin-enhanced green fluorescent protein (EGFP) transgenic mice and transplanted as a single cell suspension. In both hosts, grafted cells generated all major cerebellar phenotypes, with a precise localization in the recipient cortex or white matter. Nevertheless, the phenotypic distributions showed striking quantitative differences. Most notably, in the pcd cerebellum there was a higher amount of Purkinje cells, while other phenotypes were less frequent. Analysis of cell proliferation by 5-bromo-2'-deoxyuridine (BrDU) incorporation revealed that in both hosts mitotic activity was strongly reduced shortly after transplantation, and virtually all donor Purkinje cells were actually generated before grafting. Together, these results indicate that some compensatory mechanisms operate in the pcd environment. However, the very low mitotic rate of transplanted cells suggests that the adult cerebellum, either wild-type or mutant, does not provide instructive neurogenic cues to direct the specification of uncommitted progenitors. Rather, specific replacement in mutant hosts is achieved through selective mechanisms that favour the survival and integration of donor Purkinje cells at the expense of other phenotypes.
成体中枢神经系统(CNS)中神经元变性后的细胞替代取决于特定信号的可用性,这些信号可指导新生神经元的特化、分化以及融入成熟神经回路。近期有报道表明,在成体受伤的中枢神经系统中神经源性信号可能会重新激活,在此我们探究在浦肯野细胞变性后的小脑是否表达此类信号。因此,我们比较了移植到成年野生型和浦肯野细胞变性(pcd)突变型小鼠小脑中的胚胎小脑细胞的命运。供体细胞取自β-肌动蛋白增强型绿色荧光蛋白(EGFP)转基因小鼠,并作为单细胞悬液进行移植。在两种宿主中,移植的细胞均产生了所有主要的小脑表型,并精确地定位于受体皮质或白质中。然而,表型分布显示出显著的数量差异。最值得注意的是,在pcd小鼠的小脑中,浦肯野细胞的数量较多,而其他表型则较少见。通过5-溴-2'-脱氧尿苷(BrDU)掺入法分析细胞增殖情况,结果显示在两种宿主中,移植后不久有丝分裂活性均大幅降低,实际上所有供体浦肯野细胞都是在移植前产生的。综上所述,这些结果表明在pcd环境中存在一些补偿机制。然而,移植细胞极低的有丝分裂率表明,无论是野生型还是突变型的成年小脑,都不会提供指导性的神经源性信号来指导未分化祖细胞的特化。相反,突变宿主中的特异性替代是通过选择性机制实现的,这些机制有利于供体浦肯野细胞的存活和整合,而以牺牲其他表型为代价。