Vernadakis A
Department of Psychiatry, University of Colorado School of Medicine, Denver 80262.
Int Rev Neurobiol. 1988;30:149-224.
Considerable progress in our understanding of neuron and glial cell interrelationships has emerged during the last decade from in vitro and in vivo studies. Neural culture systems have provided powerful tools to delineate cellular and molecular events. Moreover, the advances in development of immunocytochemical and biochemical specific cell markers has made possible the characterization of complex cell behaviors. Glial cells actively participate in several aspects of neuronal growth and differentiation both by providing cell-cell contact interactions and by secreting neuronal growth-promoting factors. In turn, neurons influence the cellular behavior of both astrocytes and oligodendrocytes, primarily by secreting substances into the microenvironment. Such substances as neurohormones and neurotransmitters have been shown to affect several glial functions including electrophysiological responses, energy metabolism, and ionic homeostasis. In several instances these effects appear to be mediated through receptors on glial cells. Astrocytes actively participate in the regulation of the ionic environment. They take up and release several neurotransmitter substances and can modulate the concentration of a neurotransmitter substance at the synaptic cleft and thus monitor neuronal activity. The evidence of neuron-astroglia synaptic contacts supports the view that such contacts are present during early neuroembryogenesis and thus may provide contact signals for neuronal growth. The process of myelination in the CNS appears to be regulated by both neuronal signals to the oligodendrocyte and also intrinsic programming in the oligodendrocytes to produce myelin components. The prevailing view that astrocytes impede regeneration appears to be shifting towards a more favorable notion of the role of these cells in promoting this process. Of interest is the concept that there is a critical period in the ability of astrocytes either to enhance regeneration or to form a gliotic scar and impede this process. The role of glial cells in the aging process of the neuron is only beginning to be appreciated. If glial cells are actively involved in the regulation of the microenvironment, then it follows that any changes in the behavior of glial cells with aging will ultimately affect neuronal function. It is abundantly clear from in vitro studies that glial cells are pluripotential cells with several functional capabilities. Their responsiveness to an environment in which neurons are maturing as compared to an environment where neurons are injured or aging clearly portrays the multifunctional role of the astrocyte.(ABSTRACT TRUNCATED AT 400 WORDS)
在过去十年中,体外和体内研究使我们对神经元与神经胶质细胞的相互关系有了相当大的进展。神经培养系统提供了强大的工具来描绘细胞和分子事件。此外,免疫细胞化学和生化特异性细胞标志物开发方面的进展使得表征复杂的细胞行为成为可能。神经胶质细胞通过提供细胞间接触相互作用以及分泌神经元生长促进因子,积极参与神经元生长和分化的多个方面。反过来,神经元主要通过向微环境中分泌物质来影响星形胶质细胞和少突胶质细胞的细胞行为。已证明神经激素和神经递质等物质会影响多种神经胶质细胞功能,包括电生理反应、能量代谢和离子稳态。在一些情况下,这些作用似乎是通过神经胶质细胞上的受体介导的。星形胶质细胞积极参与离子环境的调节。它们摄取和释放多种神经递质物质,并可调节突触间隙处神经递质物质的浓度,从而监测神经元活动。神经元与星形胶质细胞突触接触的证据支持了这样一种观点,即这种接触在神经胚胎发育早期就已存在,因此可能为神经元生长提供接触信号。中枢神经系统中的髓鞘形成过程似乎受神经元向少突胶质细胞发出的信号以及少突胶质细胞中产生髓鞘成分的内在程序的共同调节。认为星形胶质细胞会阻碍再生的主流观点似乎正转向对这些细胞在促进这一过程中作用的更有利看法。有趣的是,有这样一个概念,即星形胶质细胞增强再生或形成胶质瘢痕并阻碍这一过程的能力存在关键时期。神经胶质细胞在神经元衰老过程中的作用才刚刚开始被认识到。如果神经胶质细胞积极参与微环境的调节,那么随着衰老,神经胶质细胞行为的任何变化最终都会影响神经元功能。从体外研究中可以清楚地看出,神经胶质细胞是具有多种功能能力的多能细胞。与神经元受伤或衰老的环境相比,它们对神经元成熟环境的反应清楚地描绘了星形胶质细胞的多功能作用。(摘要截选至400字)