Zanjani H S, Vogel M W, Delhaye-Bouchaud N, Martinou J C, Mariani J
Laboratoire de Neurobiologie du Développement, Institut des Neurosciences et URA CNRS 1488, Université Pierre et Marie Curie, Paris, France.
J Comp Neurol. 1996 Oct 21;374(3):332-41. doi: 10.1002/(SICI)1096-9861(19961021)374:3<332::AID-CNE2>3.0.CO;2-2.
The Purkinje cell is a primary organizer in the development of the cerebellum. Purkinje cells may provide positional information cues that regulate afferent innervation, and Purkinje cell target size controls the adult number of afferent olivary neurons and granule cells. While Purkinje cells are necessary for the survival of olivary neurons and granule cells during periods of programmed cell death, little is known about the survival requirements of Purkinje cells in vivo. To determine if Purkinje cells are subject to programmed cell death during development we have analyzed Purkinje cell numbers in two lines of transgenic mice that overexpress a human gene for bcl-2 (Hu-bcl-2). Bcl-2 is a protooncogene that inhibits apoptosis in many cell types. Overexpression of bcl-2 in vitro and in vivo rescues neurons from trophic factor deprivation or naturally occurring cell death. In the mice analyzed in this study, transgene expression is driven by the neuron-specific enolase promoter that is first expressed embryonically in most regions of the brain in one line and postnatally in the second line. We have counted Purkinje cells in three adult control mice, five early overexpressing transgenics, and three late expressing transgenics. The number of Purkinje cells in the Hu-bcl-2 transgenic mice is significantly increased above control numbers, with an increase of 43% in the embryonically overexpressing line and an increase of 27% in the postnatally overexpressing line. Because bcl-2 overexpression has been shown to rescue other neurons from programmed cell death, the increase in Purkinje cell numbers in overexpressing bcl-2 transgenics suggests that Purkinje cells undergo a period of cell death during normal development.
浦肯野细胞是小脑发育过程中的主要组织者。浦肯野细胞可能提供调节传入神经支配的位置信息线索,并且浦肯野细胞靶标的大小控制终末传入橄榄核神经元和颗粒细胞的数量。虽然在程序性细胞死亡期间,浦肯野细胞对于橄榄核神经元和颗粒细胞的存活是必需的,但关于浦肯野细胞在体内的存活需求却知之甚少。为了确定浦肯野细胞在发育过程中是否会发生程序性细胞死亡,我们分析了两种过表达人类bcl-2基因(Hu-bcl-2)的转基因小鼠品系中的浦肯野细胞数量。Bcl-2是一种原癌基因,可抑制多种细胞类型中的细胞凋亡。在体外和体内过表达bcl-2可使神经元免受营养因子剥夺或自然发生的细胞死亡。在本研究中分析的小鼠中,转基因表达由神经元特异性烯醇化酶启动子驱动,该启动子在一个品系中首先在胚胎期在大脑的大多数区域表达,在第二个品系中在出生后表达。我们对三只成年对照小鼠、五只早期过表达转基因小鼠和三只晚期表达转基因小鼠中的浦肯野细胞进行了计数。Hu-bcl-2转基因小鼠中的浦肯野细胞数量显著高于对照数量,胚胎期过表达品系增加了43%,出生后过表达品系增加了27%。由于已证明过表达bcl-2可使其他神经元免受程序性细胞死亡,过表达bcl-2转基因小鼠中浦肯野细胞数量的增加表明浦肯野细胞在正常发育过程中经历了一个细胞死亡阶段。