Division of Glial Disease and Therapeutics, Center for Translational Neuromedicine, Department of Neurosurgery, University of Rochester Medical Center, Rochester, NY 14642, USA.
Cell Calcium. 2010 Feb;47(2):140-9. doi: 10.1016/j.ceca.2009.11.010. Epub 2009 Dec 31.
The evolution of the central nervous system (CNS) resulted in an appearance of highly specialised neuronal networks optimised for rapid information transfer. In the course of this specialisation neuronal cells lost their metabolic independence and the ability to survive in the absence of homeostatic systems. These homeostatic systems, represented by neuroglia regulate all aspects of CNS function in physiological and pathological conditions. The neurological diseases should be therefore considered as primary gliopathologies, which determine the progression and outcome of neuropathological process. Glial function is intimately regulated by cellular calcium signalling that underlies the specific form of "glial calcium excitability". Glial Ca2+ signals are triggered by activation of multiple receptors, and are primarily driven by Ca2+ release from the endoplasmic reticulum. In this review we summarise the role of glial calcium signalling in various forms of pathological processes including neurological and psychiatric disorders and neurodegeneration.
中枢神经系统(CNS)的进化导致了高度专业化的神经元网络的出现,这些网络优化了快速信息传递。在这个专业化的过程中,神经元细胞失去了代谢独立性和在没有体内平衡系统的情况下生存的能力。这些体内平衡系统由神经胶质细胞代表,调节 CNS 在生理和病理条件下的所有功能方面。因此,应该将神经疾病视为原发性神经胶质病理学,这决定了神经病理过程的进展和结果。胶质细胞功能受到细胞钙信号的密切调节,而钙信号是特定形式的“胶质钙兴奋性”的基础。胶质细胞 Ca2+信号由多种受体的激活触发,主要由内质网 Ca2+释放驱动。在这篇综述中,我们总结了胶质细胞钙信号在包括神经和精神障碍以及神经退行性变在内的各种病理过程中的作用。
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