Tian Yixiang, Wu Xing, Zhang Zihao, Li Yijie, Hou Meng, Jiang Ruirui, Li Donghua, Zhang Yanhua, Guo Yulong, Li Guoxi, Liu Xiaojun, Kang Xiangtao, Tian Yadong, Li Wenting, Li Yuetao
College of Animal Science and Technology, Henan Institute of Science and Technology, Xinxiang 453003, China.
College of Animal Science and Technology, Henan Agricultural University, Zhengzhou 450046, China.
Poult Sci. 2025 Jan;104(1):104624. doi: 10.1016/j.psj.2024.104624. Epub 2024 Dec 7.
MiRNAs are typically reported to play a negative regulatory role in post-transcriptional expression of target genes and are widely involved in a variety of biological processes such as growth, metabolism and reproduction. However, research on the role of miRNAs in the ovulation process of chicken ovaries is still insufficient compared to that in mammals. Here, we investigated the regulatory mechanisms of gga-miR-6634-5p in the growth and steroid hormone secretion of chicken granulosa cells (GCs) by targeting MMP16. We found that gga-miR-6634-5p significantly down-regulated the mRNA levels of proliferation-related genes (CCND1, CDK1, and CDK6), decreased cell viability, the number of EdU-labelled positive cells, and the percentage of S-phase cells, as analysed by quantitative real time PCR (qRT-PCR), cell counting kit-8 (CCK-8), 5-ethynyl-2'deoxyuridine (EdU) and flow cytometry analyses (P < 0.01 or P < 0.05). qRT-PCR and enzyme-linked immunosorbent assay (ELISA) results demonstrated that gga-miR-6634-5p up-regulated the expression of steroid synthesis-related genes (CYP19A1, 3β-HSD, StAR and FSHR) (P < 0.01 or P < 0.05), as well as the secretion of estradiol (E2) and progesterone (P4) (P < 0.01 or P < 0.05). Furthermore, we found that MMP16 protein and gene expression can be down-regulated by gga-miR-6634-5p and demonstrated that MMP16 is a target gene of gga-miR-6634-5p by dual luciferase reporter assay (P < 0.05). In addition, we found that MMP16 stimulated the proliferation of GCs, significantly inhibited the expression of steroid synthesis related genes (CYP19A1, StAR, 3β-HSD and FSHR), and decreased the secretion of E2 and P4 (P < 0.01 or P < 0.05), which was consistent with the inhibitory effect of gga-miR-6634-5p. It was further found by functional enrichment analysis, qRT-PCR, western blot (WB) and ELISA that MMP16 may play a regulatory role in GCs proliferation as well as steroid hormone secretion through the mTOR signaling pathway and PPAR signaling pathway. Therefore, this study demonstrates that gga-miR-6634-5p modulates the proliferation of chicken GCs and the secretion of steroid hormones by targeting MMP16, which may contribute to a better understanding of the functional mechanisms of miRNAs in the ovarian development of laying hens.
通常报道称,微小RNA(miRNAs)在靶基因的转录后表达中发挥负调控作用,并广泛参与生长、代谢和繁殖等多种生物学过程。然而,与哺乳动物相比,关于miRNAs在鸡卵巢排卵过程中作用的研究仍不充分。在此,我们通过靶向基质金属蛋白酶16(MMP16)研究了gga-miR-6634-5p对鸡颗粒细胞(GCs)生长和类固醇激素分泌的调控机制。我们发现,通过定量实时荧光定量PCR(qRT-PCR)、细胞计数试剂盒-8(CCK-8)、5-乙炔基-2'-脱氧尿苷(EdU)和流式细胞术分析,gga-miR-6634-5p显著下调增殖相关基因(CCND1、CDK1和CDK6)的mRNA水平,降低细胞活力、EdU标记阳性细胞数量和S期细胞百分比(P<0.01或P<0.05)。qRT-PCR和酶联免疫吸附测定(ELISA)结果表明,gga-miR-6634-5p上调类固醇合成相关基因(CYP19A1、3β-羟基类固醇脱氢酶、类固醇生成急性调节蛋白和促卵泡激素受体)的表达(P<0.01或P<0.05),以及雌二醇(E2)和孕酮(P4)的分泌(P<0.01或P<0.05)。此外,我们发现gga-miR-6634-5p可下调MMP16蛋白和基因表达,并通过双荧光素酶报告基因测定证明MMP16是gga-miR-6634-5p的靶基因(P<0.05)。此外,我们发现MMP16刺激GCs增殖,显著抑制类固醇合成相关基因(CYP19A1、类固醇生成急性调节蛋白、3β-羟基类固醇脱氢酶和促卵泡激素受体)的表达,并降低E2和P4的分泌(P<0.01或P<0.05),这与gga-miR-6634-5p的抑制作用一致。通过功能富集分析、qRT-PCR、蛋白质免疫印迹(WB)和ELISA进一步发现,MMP16可能通过mTOR信号通路和PPAR信号通路在GCs增殖以及类固醇激素分泌中发挥调节作用。因此,本研究表明gga-miR-6634-5p通过靶向MMP16调节鸡GCs的增殖和类固醇激素的分泌,这可能有助于更好地理解miRNAs在蛋鸡卵巢发育中的功能机制。