Davies Alun M
Department of Preclinical Veterinary Sciences, Royal (Dick) School of Veterinary Studies, Summerhall Square, Edinburgh EH9 1QH, UK.
EMBO J. 2003 Jun 2;22(11):2537-45. doi: 10.1093/emboj/cdg254.
Cell death is a prominent feature of the developing vertebrate nervous system, affecting neurons, glial cells and their progenitors. The most extensively studied and best understood phase of cell death occurs in populations of neurons shortly after they begin establishing connections with other neurons and/or non-neural tissues. This phase of cell death makes appropriate adjustments to the relative sizes of interconnected groups of neurons and matches the size of neuronal populations that innervate non-neural tissues to the optimal requirements of these tissues. The fate of neurons during this period of development is regulated by a variety of secreted proteins that either promote survival or bring about cell death after binding to receptors expressed on the neurons. These proteins may be derived from the targets the neurons innervate, the afferents they receive or from associated glial cells, or they may be secreted by the neurons themselves. In this review, I will outline the established and emerging principles that modulate neuronal number in the developing nervous system.
细胞死亡是发育中的脊椎动物神经系统的一个显著特征,影响神经元、神经胶质细胞及其祖细胞。细胞死亡研究最广泛且理解最深入的阶段发生在神经元群体开始与其他神经元和/或非神经组织建立连接后不久。这个细胞死亡阶段对相互连接的神经元群体的相对大小进行适当调整,并使支配非神经组织的神经元群体大小与这些组织的最佳需求相匹配。在这个发育时期,神经元的命运受多种分泌蛋白调节,这些蛋白与神经元上表达的受体结合后,要么促进存活,要么导致细胞死亡。这些蛋白可能来自神经元支配的靶标、它们接收的传入神经或相关的神经胶质细胞,也可能由神经元自身分泌。在这篇综述中,我将概述调节发育中神经系统神经元数量的既定原则和新出现的原则。