MicroRNA-19a靶向成纤维细胞生长因子诱导分子14并预防脓毒性AKI的小管损伤。

IF 2.6 4区 医学 Q3 CELL BIOLOGY Analytical Cellular Pathology Pub Date : 2020-07-01 eCollection Date: 2020-01-01 DOI:10.1155/2020/2894650
Jun Hong, Bang-Chuan Hu, Liang Xu, Yang Zheng, Zi-Qiang Shao, Run Zhang, Xiang-Hong Yang, Ren-Hua Sun, Shi-Jing Mo
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引用次数: 7

摘要

成纤维细胞生长因子诱导分子14 (Fn14)在脓毒性急性肾损伤(AKI)中触发肾小管损伤中起主要作用。在这里,我们探讨了脓毒性AKI中Fn14失调的机制。我们发现Fn14是miR-19a的真正靶标,它直接结合Fn14的3' UTR,独立于miR-19a下游的去泛素酶(DUB),抑制柱状瘤病(CYLD),从而拮抗lps诱导的小管细胞凋亡。基因消融Fn14,而不是CYLD,消除了miR-19a通过脂多糖(LPS)拮抗小管凋亡的能力。在小鼠中,miR-19a的全身递送可以保护小鼠免受脓毒性AKI的侵害。我们的研究结果表明,miR-19a可能是预防脓毒性AKI的一种有希望的治疗候选药物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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MicroRNA-19a Targets Fibroblast Growth Factor-Inducible Molecule 14 and Prevents Tubular Damage in Septic AKI.
Fibroblast growth factor-inducible molecule 14 (Fn14) plays a principal role in triggering tubular damage during septic acute kidney injury (AKI). Here, we explore the mechanism underlying Fn14 deregulation in septic AKI. We identify Fn14 as a bona fide target of miR-19a, which directly binds to 3′ UTR of Fn14 for repression independent of cylindromatosis (CYLD), the deubiquitinase (DUB) downstream of miR-19a, and thereby antagonizes the LPS-induced tubular cell apoptosis. Genetic ablation of Fn14, but not of CYLD, abolishes the ability of miR-19a to antagonize the tubular apoptosis by lipopolysaccharide (LPS). In mice, systemic delivery of miR-19a confers protection against septic AKI. Our findings implicate that miR-19a may serve as a promising therapeutic candidate in the prevention of septic AKI.
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来源期刊
Analytical Cellular Pathology
Analytical Cellular Pathology ONCOLOGY-CELL BIOLOGY
CiteScore
4.90
自引率
3.10%
发文量
70
审稿时长
16 weeks
期刊介绍: Analytical Cellular Pathology is a peer-reviewed, Open Access journal that provides a forum for scientists, medical practitioners and pathologists working in the area of cellular pathology. The journal publishes original research articles, review articles, and clinical studies related to cytology, carcinogenesis, cell receptors, biomarkers, diagnostic pathology, immunopathology, and hematology.
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