Your browser doesn't support javascript.
loading
Ssc-miR-429 expression proliles and functions on inducing Leydig cells apoptosis.
Tang, Qi; Zhang, Yanghai; Yue, Linxiu; Ren, Hongying; Pan, Chuanying.
Afiliación
  • Tang Q; College of Animal Science and Technology, Northwest A&F University, Yangling, Shaanxi, 712100, PR China.
  • Zhang Y; Department of Animal and Dairy Sciences, University of Wisconsin-Madison, WI, 53706, United States.
  • Yue L; College of Animal Science and Technology, Northwest A&F University, Yangling, Shaanxi, 712100, PR China.
  • Ren H; College of Animal Science and Technology, Northwest A&F University, Yangling, Shaanxi, 712100, PR China.
  • Pan C; College of Animal Science and Technology, Northwest A&F University, Yangling, Shaanxi, 712100, PR China. Electronic address: chuanyingpan@126.com.
Theriogenology ; 216: 62-68, 2024 Mar 01.
Article en En | MEDLINE | ID: mdl-38157808
ABSTRACT
Leydig cells (LCs) play an indispensable role in testosterone synthesis, and their dysfunction can result in male reproductive disorders. Previous transcriptome sequencing revealed differential expression of MicroRNA-429 (miR-429) in both Leydig stem cells (SLCs) and LCs, indicating its potential regulatory function in LCs. In this study, we examined the expression of miR-429 in seven pig tissues (heart, liver, spleen, lung, kidney, testis, epididymis, brain) and investigated its impact on the proliferation and apoptosis of testicular interstitial cells using various techniques such as CCK-8, EdU, TUNEL, Western blot, among others. The results demonstrated that miR-429 exhibited lower expression levels in the testis, particularly in the LCs of testicular tissue. Upon upregulation of miR-429, TM3 cell density significantly increased, while downregulation led to a slight elevation in cell density. Further research indicated that the observed phenotype was due to miR-429-induced cell apoptosis, independent of cell proliferation. Additionally, a dual-luciferase reporter system revealed no targeting relationship between miR-429 and the predicted target genes (BMI1 and SOX5). Previous reports confirm Bcl2 as a known target of miR-429, leading us to hypothesize that miR-429 diminishes LCs' anti-apoptotic capability by inhibiting Bcl2. In summary, our findings suggest that miR-429 may induce LC apoptosis, supporting its potential as a biomarker for male reproductive disorders linked to Leydig cell dysfunction.
Asunto(s)
Palabras clave

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: MicroARNs / Células Intersticiales del Testículo Límite: Animals Idioma: En Revista: Theriogenology Año: 2024 Tipo del documento: Article Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: MicroARNs / Células Intersticiales del Testículo Límite: Animals Idioma: En Revista: Theriogenology Año: 2024 Tipo del documento: Article Pais de publicación: Estados Unidos