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Cell · 2021

Multi-organ proteomic landscape of COVID-19 autopsies.

Клиническое исследованиеСтатьяМногоцентровое исследованиеПоддержка исследования: вне правительства СШАНазвание и аннотация: Перевод в очереди
Обработка статьи · этапы, ошибки и управление
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Nie Xiu, Qian Liujia, Sun Rui, Huang Bo, Dong Xiaochuan, Xiao Qi, Zhang Qiushi, Lu Tian, Yue Liang, Chen Shuo, Li Xiang, Sun Yaoting, Li Lu, Xu Luang, Li Yan, Yang Ming, Xue Zhangzhi, Liang Shuang, Ding Xuan, Yuan Chunhui, Peng Li, Liu Wei, Yi Xiao, Lyu Mengge, Xiao Guixiang, Xu Xia, Ge Weigang, He Jiale, Fan Jun, Wu Junhua, Luo Meng, Chang Xiaona, Pan Huaxiong, Cai Xue, Zhou Junjie, Yu Jing, Gao Huanhuan, Xie Mingxing, Wang Sihua, Ruan Guan, Chen Hao, Su Hua, Mei Heng, Luo Danju, Zhao Dashi, Xu Fei, Li Yan, Zhu Yi, Xia Jiahong, Hu Yu, Guo Tiannan

Аннотация

The molecular pathology of multi-organ injuries in COVID-19 patients remains unclear, preventing effective therapeutics development. Here, we report a proteomic analysis of 144 autopsy samples from seven organs in 19 COVID-19 patients. We quantified 11,394 proteins in these samples, in which 5,336 were perturbed in the COVID-19 patients compared to controls. Our data showed that cathepsin L1, rather than ACE2, was significantly upregulated in the lung from the COVID-19 patients. Systemic hyperinflammation and dysregulation of glucose and fatty acid metabolism were detected in multiple organs. We also observed dysregulation of key factors involved in hypoxia, angiogenesis, blood coagulation, and fibrosis in multiple organs from the COVID-19 patients. Evidence for testicular injuries includes reduced Leydig cells, suppressed cholesterol biosynthesis, and sperm mobility. In summary, this study depicts a multi-organ proteomic landscape of COVID-19 autopsies that furthers our understanding of the biological basis of COVID-19 pathology.

Предметные рубрики MeSH

ИП Урсолов Владлен Сергеевич

ИНН 500118482352 · ОГРНИП 314500117700049

Реквизиты и контакты