Yamada Tatsuya, Adachi Yoshihiro, Fukaya Masahiro, Iijima Miho, Sesaki Hiromi
Department of Cell Biology, Johns Hopkins University School of Medicine, Baltimore, Maryland.
Department of Anatomy, Kitasato University School of Medicine, Sagamihara, Kanagawa, Japan.
Am J Pathol. 2016 Nov;186(11):2798-2802. doi: 10.1016/j.ajpath.2016.06.025. Epub 2016 Sep 15.
Mitochondria are dynamic organelles that divide and fuse to modulate their number and shape. We have previously reported that the loss of dynamin-related protein 1 (Drp1), which mediates mitochondrial division, leads to the degeneration of cerebellar Purkinje cells in mice. Because Drp1 has been shown to be important for apoptosis and necroptosis, it is puzzling how Purkinje neurons die in the absence of Drp1. In this study, we tested whether neurodegeneration involves necrotic cell death by generating Purkinje cell-specific Drp1-knockout (KO) mice that lack the receptor-interacting protein kinase 3 (Rip3), which regulates necroptosis. We found that the loss of Rip3 significantly delays the degeneration of Drp1-KO Purkinje neurons. In addition, before neurodegeneration, mitochondrial tubules elongate because of unopposed fusion and subsequently become large spheres as a result of oxidative damage. Surprisingly, Rip3 loss also helps Drp1-KO Purkinje cells maintain the elongated morphology of the mitochondrial tubules. These data suggest that Rip3 plays a role in neurodegeneration and mitochondrial morphology in the absence of mitochondrial division.
线粒体是动态细胞器,可进行分裂和融合以调节其数量和形态。我们之前报道过,介导线粒体分裂的动力相关蛋白1(Drp1)缺失会导致小鼠小脑浦肯野细胞退化。由于Drp1已被证明对凋亡和坏死性凋亡很重要,因此在没有Drp1的情况下浦肯野神经元如何死亡令人费解。在本研究中,我们通过构建缺乏调节坏死性凋亡的受体相互作用蛋白激酶3(Rip3)的浦肯野细胞特异性Drp1基因敲除(KO)小鼠,来测试神经退行性变是否涉及坏死性细胞死亡。我们发现,Rip3缺失显著延迟了Drp1-KO浦肯野神经元的退化。此外,在神经退行性变之前,线粒体小管因无对抗的融合而延长,随后由于氧化损伤而变成大球体。令人惊讶的是,Rip3缺失也有助于Drp1-KO浦肯野细胞维持线粒体小管的延长形态。这些数据表明,在没有线粒体分裂的情况下,Rip3在神经退行性变和线粒体形态中发挥作用。