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miR-7 通过 JAK/STAT3 信号通路靶向 KLF4 促进鸡颗粒细胞凋亡和自噬。

miR-7 promotes apoptosis and autophagy of granulosa cells by targeting KLF4 via JAK/STAT3 signaling pathway in chickens.

机构信息

Key Laboratory of Livestock and Poultry Multi-omics, Ministry of Agriculture and Rural Affairs, College of Animal Science and Technology, Sichuan Agricultural University, Chengdu, 611130, Sichuan, China; Farm Animal Genetic Resources Exploration and Innovation Key Laboratory of Sichuan Province, Sichuan Agricultural University, Chengdu, 611130, Sichuan, China.

Animal Breeding and Genetics Key Laboratory of Sichuan Province, Sichuan Animal Science Academy, Chengdu, 610066, China.

出版信息

Theriogenology. 2024 Dec;230:322-329. doi: 10.1016/j.theriogenology.2024.09.032. Epub 2024 Sep 29.

Abstract

Granulosa cell (GC) death, which leads to follicular atresia, primarily occurs through apoptosis and autophagy. miRNAs are known to be key regulators of autophagy and apoptosis. Although miR-7 acting as a key regulator of follicular atresia, its precise role in granulosa cell autophagy and apoptosis remains to be fully elucidated. In this study, we found that miR-7 was highly expressed in the follicle based on qPCR analysis. Subsequently, transfection of miR-7 inhibitors and mimics downregulated or upregulated the expression of miR-7 and promoted autophagic and apoptotic processes in chicken follicle granulosa cells. Mechanistically, through dual-luciferase reporter gene assays, we validated that KLF4 is a target gene of miR-7. Contrarily, KLF4 was found to negatively regulate autophagy and apoptosis in follicular granulosa cells as evidenced by genetic intervention of KLF4 silencing and overexpression. Furthermore, JAK/STAT3 signaling pathway was confirmed to mediate the regulation of miR-7-KLF4 axis on GC autophagy and apoptosis. These findings offer evidences of the crucial involvement of the miR-7-KLF4 signaling axis in determining autophagy and apoptosis of GCs. This study could offer an important theoretical basis for the use of molecular-assisted breeding in chickens.

摘要

颗粒细胞 (GC) 死亡导致卵泡闭锁,主要通过细胞凋亡和自噬发生。miRNA 是自噬和凋亡的关键调节因子。尽管 miR-7 作为卵泡闭锁的关键调节因子,但它在颗粒细胞自噬和凋亡中的精确作用仍有待充分阐明。在这项研究中,我们发现 qPCR 分析表明 miR-7 在卵泡中高表达。随后,miR-7 抑制剂和模拟物的转染下调或上调了 miR-7 的表达,并促进了鸡卵泡颗粒细胞的自噬和凋亡过程。通过双荧光素酶报告基因检测,我们验证了 KLF4 是 miR-7 的靶基因。相反,通过沉默和过表达 KLF4 的遗传干预,发现 KLF4 负调控卵泡颗粒细胞中的自噬和凋亡。此外,证实 JAK/STAT3 信号通路介导了 miR-7-KLF4 轴对 GC 自噬和凋亡的调节。这些发现为 miR-7-KLF4 信号轴在决定 GC 自噬和凋亡中的关键作用提供了证据。这项研究可为鸡的分子辅助育种提供重要的理论基础。

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