Ilsong Institute of Life Science, Hallym University, Anyang, Gyeonggi-do, Republic of Korea.
Department of Biomedical Gerontology, Graduate School of Hallym University, Chuncheon, Gangwon-do, Republic of Korea.
Neuropathol Appl Neurobiol. 2020 Dec;46(7):751-769. doi: 10.1111/nan.12620. Epub 2020 May 1.
Vimentin citrullination, the calcium (Ca )-dependent peptidylarginine deiminase (PAD)-mediated conversion of an arginine residue of vimentin to a citrulline residue, has emerged as a pathophysiological outcome of autoimmune diseases and neurodegeneration. However, the roles, functions, and expression of citrullinated vimentin have not yet been elucidated because available antibodies are limited.
We developed mouse monoclonal IgG1 and IgM specific for vimentin citrullinated at position R440 or R450 and applied Western blotting, immunohistochemistry, and immunofluorescent staining to investigate the pathogenesis of prion diseases in animal models, in patients with prion diseases, and in vitro.
Vimentin was found to be highly citrullinated at R440 and R450, and these citrullinated forms were mainly expressed in reactive astrocytes in the brain tissues of scrapie-infected mice. Full-length and cleaved forms of citrullinated vimentin were found in the cerebral cortices of sporadic Creutzfeldt-Jakob disease (sCJD) patients. The distribution of citrullinated vimentin was mainly confirmed in vimentin-, GFAP-, and YKL-40-positive reactive astrocytes. Biochemically, citrullination promoted resistance to the caspase-3- and caspase-9-mediated fragmentation of vimentin. Additionally, citrullination led to increased cytoplasmic and integral membrane/organelle vimentin enrichment, which indicated changes in the intrinsic solubility and distribution of vimentin.
Our observations suggest that citrullinated vimentin acts as a specific indicator for the reactive state of astrocytes under abnormal neurological conditions. In addition, these novel antibodies will be helpful for studying the role of citrullinated vimentin in the pathogenesis of human disorders.
波形蛋白瓜氨酸化是一种病理生理结果,由钙(Ca )依赖性肽基精氨酸脱亚氨酶(PAD)介导,将波形蛋白的精氨酸残基转化为瓜氨酸残基,它已成为自身免疫性疾病和神经退行性变的发病机制。然而,由于可用的抗体有限,瓜氨酸化波形蛋白的作用、功能和表达尚未阐明。
我们开发了针对位置 R440 或 R450 瓜氨酸化的波形蛋白的小鼠单克隆 IgG1 和 IgM,并应用 Western blot、免疫组织化学和免疫荧光染色来研究动物模型、朊病毒病患者和体外的朊病毒病的发病机制。
发现波形蛋白在 R440 和 R450 高度瓜氨酸化,这些瓜氨酸化形式主要在朊病毒感染小鼠的脑组织中的反应性星形胶质细胞中表达。全长和裂解形式的瓜氨酸化波形蛋白在散发性克雅氏病(sCJD)患者的大脑皮质中被发现。瓜氨酸化波形蛋白的分布主要在波形蛋白、GFAP 和 YKL-40 阳性反应性星形胶质细胞中被证实。从生物化学角度来看,瓜氨酸化促进了波形蛋白对 caspase-3 和 caspase-9 介导的片段化的抵抗。此外,瓜氨酸化导致细胞质和完整膜/细胞器波形蛋白丰度增加,表明波形蛋白的内在可溶性和分布发生变化。
我们的观察结果表明,瓜氨酸化波形蛋白作为异常神经条件下星形胶质细胞反应状态的特异性指标。此外,这些新的抗体将有助于研究瓜氨酸化波形蛋白在人类疾病发病机制中的作用。