Sayer Rod J
Department of Physiology, University of Otago, PO Box 913, Dunedin, New Zealand.
Adv Exp Med Biol. 2002;513:183-96. doi: 10.1007/978-1-4615-0123-7_6.
Intracellular Ca2+ is regulated within three major compartments: the cytosol, the endoplasmic reticulum and mitochondria. This Chapter reviews the mechanisms involved in handling of Ca2+ within these compartments with reference to potential strategies for neuroprotection. In the cytosol, Ca2+ buffering has a major influence on Ca2+ signals. Cytosolic Ca(2+)-binding proteins such as CB28 participate in Ca2+ buffering and may have a role in resistance to neurotoxicity. In the endoplasmic reticulum, a number of proteins are involved in Ca2+ uptake, lumenal buffering or release, and these may be of value as potential targets for therapeutic intervention. Mitochondria are receiving increasing attention for their role in Ca2+ storage and signaling, and as key players in the processes leading to cell death following Ca2+ overload. An improved understanding of how Ca2+ is controlled within these intracellular compartments, and how these compartments interact, will be important for neuroprotective strategies.
细胞质、内质网和线粒体。本章回顾了这些区室内钙离子处理所涉及的机制,并参考了神经保护的潜在策略。在细胞质中,钙离子缓冲对钙离子信号有重大影响。细胞质中的钙离子结合蛋白如CB28参与钙离子缓冲,可能在抵抗神经毒性方面发挥作用。在内质网中,许多蛋白质参与钙离子的摄取、腔室缓冲或释放,这些可能作为治疗干预的潜在靶点具有价值。线粒体因其在钙离子储存和信号传导中的作用,以及作为钙离子过载后导致细胞死亡过程中的关键参与者而受到越来越多的关注。更好地理解这些细胞内区室中钙离子是如何被控制的,以及这些区室如何相互作用,对于神经保护策略至关重要。