School of Biological Sciences, University of Auckland, Auckland, New Zealand.
IUBMB Life. 2010 Dec;62(12):878-85. doi: 10.1002/iub.405.
Over the past decade, following the discovery of the human heme protein neuroglobin, many studies have searched for evidence for this protein's mechanism of action. Much data has accrued showing that high levels of neuroglobin will protect cells from apoptotic cell death, following a wide range of challenges. Various explanations of its actions, based on measured reactivity with oxygen, nitric oxide, or free radicals, have been proposed, but none have, as yet, been substantiated in vivo. Following preliminary experiments, it was previously hypothesised that "the central role of neuroglobin in highly metabolically active cells and retinal and brain neurons is to reset the trigger level of mitochondrial cytochrome c release necessary to commit the cells to apoptosis" (I.U.M.B.M. Life (2008) 60, 398). In this article, we review the evidence, which has accumulated to support this hypothesised mechanism of action of neuroglobin and integrate this data, with other reported intracellular functions of neuroglobin, to suggest a plausible central role for neuroglobin in the control of apoptosis.
在过去的十年中,随着人类血红素蛋白神经球蛋白的发现,许多研究都在寻找该蛋白作用机制的证据。大量数据表明,高水平的神经球蛋白可以保护细胞免受多种挑战引起的细胞凋亡。基于与氧、一氧化氮或自由基的反应性,已经提出了许多关于其作用的解释,但尚未在体内得到证实。在初步实验之后,之前假设“神经球蛋白在高度代谢活跃的细胞和视网膜和脑神经元中的核心作用是重置线粒体细胞色素 c 释放的触发水平,这是使细胞凋亡的必要条件”(国际生物医学研究组织生命(2008)60,398)。在本文中,我们回顾了支持神经球蛋白这种作用机制的证据,并将这些数据与神经球蛋白的其他报道的细胞内功能整合在一起,提出神经球蛋白在凋亡控制中的核心作用的可能性。