The Solomon H. Snyder Department of Neuroscience, Johns Hopkins University, Baltimore, MD 21205, USA.
Cell Rep. 2013 Sep 12;4(5):890-7. doi: 10.1016/j.celrep.2013.08.001. Epub 2013 Sep 5.
Huntington's disease (HD) is an autosomal-dominant neurodegenerative disease caused by the expansion of polyglutamine repeats in the gene for huntingtin (Htt). In HD, the corpus striatum selectively degenerates despite the uniform expression of mutant huntingtin (mHtt) throughout the brain and body. Striatal selectivity reflects the binding of the striatal-selective protein Rhes to mHtt to augment cytotoxicity, but molecular mechanisms underlying the toxicity have been elusive. Here, we report that the Golgi protein acyl-CoA binding domain containing 3 (ACBD3) mediates mHtt cytotoxicity via a Rhes/mHtt/ACBD3 complex. ACBD3 levels are markedly elevated in the striatum of HD patients, in a striatal cell line harboring polyglutamine repeats, and in the brains of HD mice. Moreover, ACBD3 deletion abolishes HD neurotoxicity, which is increased by ACBD3 overexpression. Enhanced levels of ACBD3 elicited by endoplasmic reticulum, mitochondrial, and Golgi stresses may account for HD-associated augmentation of ACBD3 and neurodegeneration.
亨廷顿病(HD)是一种常染色体显性神经退行性疾病,由亨廷顿基因(Htt)中多聚谷氨酰胺重复扩展引起。在 HD 中,尽管突变型亨廷顿蛋白(mHtt)在大脑和全身均匀表达,但纹状体选择性退化。纹状体选择性反映了纹状体选择性蛋白 Rhes 与 mHtt 的结合,以增强细胞毒性,但毒性的分子机制一直难以捉摸。在这里,我们报告高尔基蛋白酰基辅酶 A 结合域包含 3(ACBD3)通过 Rhes/mHtt/ACBD3 复合物介导 mHtt 细胞毒性。ACBD3 水平在 HD 患者的纹状体、携带多聚谷氨酰胺重复的纹状体细胞系和 HD 小鼠的大脑中明显升高。此外,ACBD3 缺失可消除 HD 神经毒性,而 ACBD3 过表达则增加了神经毒性。内质网、线粒体和高尔基应激引起的 ACBD3 水平升高可能解释了与 HD 相关的 ACBD3 增加和神经退行性变。