MiR-223 inhibits proliferation and steroid hormone synthesis of ovarian granulosa cell via the AKT signaling pathway by targeting CRIM1 in chicken

被引:2
|
作者
Xiang, Jialin [1 ,2 ]
Shen, Xiaoxu [1 ,2 ]
Zhang, Yao [1 ,2 ]
Zhu, Qing [1 ,2 ]
Yin, Huadong [1 ,2 ]
Han, Shunshun [1 ,2 ]
机构
[1] Sichuan Agr Univ, Coll Anim Sci & Technol, Key Lab Livestock & Poultry Multiom, Minist Agr & Rural Affairs, Chengdu 611130, Sichuan, Peoples R China
[2] Sichuan Agr Univ, Farm Anim Genet Resources Explorat & Innovat Key L, Chengdu 611130, Sichuan, Peoples R China
关键词
miR-223; CRIM1; proliferation; steroid hormone synthesis; AKT signaling pathway; FOLLICULAR-GROWTH; CYTOCHROME B(5); EXPRESSION;
D O I
10.1016/j.psj.2024.103910
中图分类号
S8 [畜牧、 动物医学、狩猎、蚕、蜂];
学科分类号
0905 ;
摘要
Within the poultry industry, hens' reproductive performance is of great economic significance. The development and growth of follicles is a key aspect of hen egg production, and ovarian follicle growth and development are closely associated with granulosa cells (GCs) proliferation and the synthesis of steroid hormones. It has been confirmed by numerous studies that microRNAs (miRNAs) play important roles in the steroid hormone synthesis and proliferation of GCs. In this study, we examined the main miRNAs influencing hens' ability to reproduce, identified the miR-223 that is mainly expressed in atretic follicles based on sequencing, and investigated its role in GCs. Then, we used miR-223 mimic and inhibitor to knockdown or overexpress miR223 expression. The result showed that miR-223 significantly inhibits both the steroid hormone synthesis and the proliferation of GCs. Subsequently, the results of the dual luciferase reporter experiment and bioinformatics prediction demonstrated that cysteine rich transmembrane BMP regulator 1 (CRIM1) was a downstream target gene of miR-223, and overexpression of miR-223 prevented CRIM1 expression. The function of CRIM1 was further investigated, and we observed a significant reduction in the synthesis of steroid hormones and the proliferation of GCs after transfection with CRIM1 siRNA. The opposite function of miR-223 was observed for CRIM1 in our study. Additionally, we demonstrated the involvement of the miR-223/ CRIM1 axis in GCs through modulation of the AKT signaling pathway. Our data demonstrate the pivotal role of the miR-223 in the proliferation and steroid hormone synthesis of chicken GCs, which helps to explain how non-coding RNA (ncRNA) affects chicken reproductive function.
引用
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页数:12
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