Kaul Sunil C, Deocaris Custer C, Wadhwa Renu
National Institute of Advanced Industrial Science and Technology, Tsukuba, Central 4, 1-1-1 Higashi, Tsukuba, Ibaraki 305 8562, Japan.
Exp Gerontol. 2007 Apr;42(4):263-74. doi: 10.1016/j.exger.2006.10.020. Epub 2006 Dec 22.
Mortalin was first cloned as a mortality factor that existed in the cytoplasmic fractions of normal, but not in immortal, mouse fibroblasts. A decade of efforts have expanded its persona from a house keeper protein involved in mitochondrial import, energy generation and chaperoning of misfolded proteins, to a guardian of stress that has multiple binding partners and to a killer protein that contributes to carcinogenesis on one hand and to old age disorders on the other. Being proved to be an attractive target for cancer therapy, it also warrants attention from the perspectives of management of old age diseases and healthy aging.
mortalin最初被克隆为一种存在于正常小鼠成纤维细胞胞质部分而非永生小鼠成纤维细胞中的死亡因子。经过十年的研究,它的角色从一种参与线粒体导入、能量生成和错误折叠蛋白伴侣功能的管家蛋白,扩展为一种具有多个结合伴侣的应激守护者,以及一种一方面促进致癌作用、另一方面导致老年疾病的杀手蛋白。由于被证明是癌症治疗的一个有吸引力的靶点,它也值得从老年疾病管理和健康老龄化的角度加以关注。