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TC1(C8orf4)是一种新型的内皮炎症调节因子,可增强核因子κB活性。

TC1(C8orf4) is a novel endothelial inflammatory regulator enhancing NF-kappaB activity.

作者信息

Kim Jungtae, Kim Yunlim, Kim Hyun-Taek, Kim Dong Wook, Ha Yunhi, Kim Jihun, Kim Cheol-Hee, Lee Inchul, Song Kyuyoung

机构信息

Asan Institute for Life Sciences, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea.

出版信息

J Immunol. 2009 Sep 15;183(6):3996-4002. doi: 10.4049/jimmunol.0900956. Epub 2009 Aug 14.

Abstract

Endothelial inflammation is regulated by a complex molecular mechanism. TC1(C8orf4) is a novel regulator implicated in cancer and inflammation. It is a small protein conserved well among vertebrates. In zebrafish embryos, it is mostly expressed in angio-hematopoietic system and the overexpression induces edema. In human aortic endothelial cells and umbilical vein endothelial cells, TC1 transfection up-regulates key inflammatory cytokines, enzymes, and adhesion proteins including IL-6, IL-1alpha, COX-2, CXCL1, CCL5, CCL2, IL-8, ICAM1, VCAM1, and E-selectin, while TC1 knockdown down-regulates them. TC1 also enhances inflammatory parameters such as monocyte-endothelial adhesion and endothelial monolayer permeability. TC1 is up-regulated by IL-1beta, TNF-alpha, LPS, and phorbol ester, and the up-regulation is inhibited by I-kappaB-kinase inhibitors. TC1, in turn, enhances the nuclear translocation of RelA and the DNA binding activity, suggesting a biological role of amplifying NF-kappaB signaling via a positive feedback. Our findings suggest that TC1 is a novel endothelial inflammatory regulator that might be implicated in inflammatory vascular diseases.

摘要

内皮细胞炎症受复杂的分子机制调控。TC1(C8orf4)是一种涉及癌症和炎症的新型调节因子。它是一种在脊椎动物中保守性良好的小蛋白。在斑马鱼胚胎中,它主要在血管造血系统中表达,过表达会诱导水肿。在人主动脉内皮细胞和脐静脉内皮细胞中,转染TC1会上调关键的炎症细胞因子、酶和黏附蛋白,包括IL-6、IL-1α、COX-2、CXCL1、CCL5、CCL2、IL-8、ICAM1、VCAM1和E-选择素,而敲低TC1则会下调它们。TC1还会增强诸如单核细胞-内皮细胞黏附以及内皮单层通透性等炎症参数。TC1会被IL-1β、TNF-α、LPS和佛波酯上调,且这种上调会被I-κB激酶抑制剂抑制。反过来,TC1会增强RelA的核转位和DNA结合活性,这表明它通过正反馈放大NF-κB信号传导具有生物学作用。我们的研究结果表明,TC1是一种新型的内皮细胞炎症调节因子,可能与炎症性血管疾病有关。

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