Hara Makoto R, Snyder Solomon H
The Solomon H. Snyder Department of Neuroscience, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA.
Annu Rev Pharmacol Toxicol. 2007;47:117-41. doi: 10.1146/annurev.pharmtox.47.120505.105311.
The past few decades have revealed that cell death can be precisely programmed with two principal forms, apoptosis and necrosis. Besides pathophysiological alterations, physiologic processes, such as the pruning of neurons during normal development and the involution of the thymus, involve apoptosis. This review focuses on the role of inter- and intracellular signaling systems in cell death, especially in the nervous system. Among neurotransmitters, glutamate and nitric oxide have been most extensively characterized and contribute to cell death in excitotoxic damage, especially in stroke and possibly in neurodegenerative diseases. Within cells, calcium, the most prominent of all intracellular messengers, mediates diverse forms of cell death with actions modulated by many proteins, including IP3 receptors, calcineurin, calpain, and cytochrome c.
在过去几十年里发现,细胞死亡可通过两种主要形式精确编程,即凋亡和坏死。除了病理生理改变外,诸如正常发育过程中神经元的修剪以及胸腺退化等生理过程也涉及凋亡。本综述重点关注细胞间和细胞内信号系统在细胞死亡中的作用,尤其是在神经系统中的作用。在神经递质中,谷氨酸和一氧化氮得到了最广泛的研究,并且在兴奋性毒性损伤中导致细胞死亡,尤其是在中风以及可能在神经退行性疾病中。在细胞内,钙作为所有细胞内信使中最突出的一种,介导多种形式的细胞死亡,其作用受到许多蛋白质的调节,包括肌醇三磷酸受体、钙调神经磷酸酶、钙蛋白酶和细胞色素c。