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从靶细胞异质性探索自身免疫性肝病的发病机制。

Exploring the Pathogenesis of Autoimmune Liver Diseases from the Heterogeneity of Target Cells.

作者信息

Qiu Zi-Xuan, Huang Lin-Xiang, Wang Xiao-Xiao, Wang Zi-Long, Li Xiao-He, Feng Bo

机构信息

Peking University People's Hospital, Peking University Hepatology Institute, Beijing Key Laboratory of Hepatitis C and Immunotherapy for Liver Diseases, Beijing International Cooperation Base for Science and Technology on NAFLD Diagnosis, Beijing, China.

出版信息

J Clin Transl Hepatol. 2024 Jul 28;12(7):659-666. doi: 10.14218/JCTH.2023.00531. Epub 2024 May 28.

Abstract

The incidence of autoimmune liver diseases (ALDs) and research on their pathogenesis are increasing annually. However, except for autoimmune hepatitis, which responds well to immunosuppression, primary biliary cholangitis and primary sclerosing cholangitis are insensitive to immunosuppressive therapy. Besides the known effects of the environment, genetics, and immunity on ALDs, the heterogeneity of target cells provides new insights into their pathogenesis. This review started by exploring the heterogeneity in the development, structures, and functions of hepatocytes and epithelial cells of the small and large bile ducts. For example, cytokeratin (CK) 8 and CK18 are primarily expressed in hepatocytes, while CK7 and CK19 are primarily expressed in intrahepatic cholangiocytes. Additionally, emerging technologies of single-cell RNA sequencing and spatial transcriptomic are being applied to study ALDs. This review offered a new perspective on understanding the pathogenic mechanisms and potential treatment strategies for ALDs.

摘要

自身免疫性肝病(ALD)的发病率及其发病机制的研究每年都在增加。然而,除了对免疫抑制反应良好的自身免疫性肝炎外,原发性胆汁性胆管炎和原发性硬化性胆管炎对免疫抑制治疗不敏感。除了已知的环境、遗传和免疫对ALD的影响外,靶细胞的异质性为其发病机制提供了新的见解。本综述首先探讨了肝细胞以及肝内外胆管上皮细胞在发育、结构和功能上的异质性。例如,细胞角蛋白(CK)8和CK18主要在肝细胞中表达,而CK7和CK19主要在肝内胆管细胞中表达。此外,单细胞RNA测序和空间转录组学等新兴技术正被应用于ALD的研究。本综述为理解ALD的致病机制和潜在治疗策略提供了新的视角。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a32/11233981/fe6ebfd56b41/JCTH-12-659-g001.jpg

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