Verkhratsky A, Toescu E C
The University of Manchester, School of Biological Sciences, Manchester, United Kingdom.
J Cell Mol Med. 2003 Oct-Dec;7(4):351-61. doi: 10.1111/j.1582-4934.2003.tb00238.x.
The endoplasmic reticulum (ER) is a universal signalling organelle, which regulates a wide range of neuronal functional responses. Calcium release from the ER underlies various forms of intracellular Ca(2+) signalling by either amplifying Ca(2+) entry through voltage-gated Ca(2+) channels by Ca(2+)-induced Ca(2+) release (CICR) or by producing local or global cytosolic calcium fluctuations following stimulation of metabotropic receptors through inositol-1,4,5-trisphosphate-induced Ca(2+) release (IICR). The ER Ca(2+) store emerges as a single interconnected pool, thus allowing for a long-range Ca(2+) signalling via intra-ER tunnels. The fluctuations of intra-ER free Ca(2+) concentration regulate the activity of numerous ER resident proteins responsible for post-translational protein folding and modification. Disruption of ER Ca(2+) homeostasis results in the developing of ER stress response, which in turn controls neuronal survival. Altered ER Ca(2+) handling may be involved in pathogenesis of various neurodegenerative diseases including brain ischemia and Alzheimer dementia.
内质网(ER)是一种普遍存在的信号细胞器,它调节多种神经元功能反应。内质网释放钙是各种形式细胞内钙信号的基础,其方式包括通过钙诱导的钙释放(CICR)放大通过电压门控钙通道的钙内流,或者在通过肌醇-1,4,5-三磷酸诱导的钙释放(IICR)刺激代谢型受体后产生局部或整体胞质钙波动。内质网钙库呈现为一个单一的相互连接的池,从而允许通过内质网内通道进行远程钙信号传递。内质网游离钙浓度的波动调节许多负责翻译后蛋白质折叠和修饰的内质网驻留蛋白的活性。内质网钙稳态的破坏导致内质网应激反应的发生,进而控制神经元的存活。内质网钙处理的改变可能参与包括脑缺血和阿尔茨海默病痴呆在内的各种神经退行性疾病的发病机制。