Silva Jillian M, Wong Alice, Carelli Valerio, Cortopassi Gino A
Department of Molecular Biosciences, University of California, Davis, 95616, USA.
Neurobiol Dis. 2009 May;34(2):357-65. doi: 10.1016/j.nbd.2009.02.005. Epub 2009 Feb 20.
Maternal inheritance of a pathogenic point mutation within complex I of the mitochondrial genome causes Leber's hereditary optic neuropathy (LHON), resulting in the neurodegeneration and demyelination of the optic nerve. The integrated stress response (ISR), a signaling pathway that responds to various stresses by activating a common set of genes, has been linked to both mitochondrial defects and demyelinating diseases. Therefore, we wanted to determine whether mitochondrial dysfunction induced by complex I inhibition with rotenone can activate the ISR, specifically by the ER kinase PERK, in oligodendroglial cells. Our complex I-deficient oligodendroglial model reproduced similar biochemical defects as in LHON by decreasing ATP synthesis and ATP levels. The same doses of rotenone that reduced ATP production also induced dose-dependent increases in PERK and eIF2alpha phosphorylation as well as activated the ISR stress genes, ATF4 and CHOP. In addition, complex I inhibition at these same concentrations induced a PERK-dependent activation of the cell death kinase, JNK, and inhibited oligodendroglial proliferation. Taken together, our results demonstrate that activation of the ISR may be one example of mitochondrial retrograde signaling in response to complex I deficiency and we suggest that this response mechanism may be relevant to the pathophysiology of LHON.
线粒体基因组复合体I内致病点突变的母系遗传会导致Leber遗传性视神经病变(LHON),进而引起视神经的神经变性和脱髓鞘。整合应激反应(ISR)是一种通过激活一组共同基因来应对各种应激的信号通路,它与线粒体缺陷和脱髓鞘疾病都有关联。因此,我们想确定用鱼藤酮抑制复合体I所诱导的线粒体功能障碍是否能在少突胶质细胞中激活ISR,特别是通过内质网激酶PERK来激活。我们的复合体I缺陷少突胶质细胞模型通过降低ATP合成和ATP水平,再现了与LHON中相似的生化缺陷。降低ATP生成的相同剂量鱼藤酮还诱导了PERK和eIF2α磷酸化的剂量依赖性增加,并激活了ISR应激基因ATF4和CHOP。此外,在这些相同浓度下抑制复合体I会诱导细胞死亡激酶JNK的PERK依赖性激活,并抑制少突胶质细胞增殖。综上所述,我们的结果表明,ISR的激活可能是线粒体对复合体I缺陷的逆行信号传导的一个例子,并且我们认为这种反应机制可能与LHON的病理生理学相关。