Possible involvement of a MEG3-miR-21-SPRY1-NF-κB feedback loop in spermatogenic cells proliferation, autophagy, and apoptosis

  • iScience. 2024 Sep 10;27(10):110904. doi: 10.1016/j.isci.2024.110904.
Xingyu Fang  1 Xiaotong Lu  1 Yujie Ma  1 Ning Sun  1 Yunyun Jiao  1 Hui Meng  2 Mengjiao Song  1 Haixia Jin  1 Guidong Yao  1 Ning Song  1 Zhaoting Wu  1 Shuang Wen  1 Haoran Guo  3 Haosen Xiong  2 Wenyan Song  1
Affiliations
  • 1. Center for Reproductive Medicine, The First Affiliated Hospital of Zhengzhou University, Zhengzhou 450052, China.
  • 2. Department of Pathology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou 450052, China.
  • 3. School of Basic Medical Sciences, Academy of Medical Sciences, Zhengzhou University, Zhengzhou, China.
Abstract

Non-obstructive azoospermia (NOA) is the most incurable form of male infertility with a complex etiology. Long non-cording RNAs (lncRNAs) were associated with regulating spermatogenesis. Herein, differentially expressed lncRNAs between NOA and control male were screened by RNA-seq analysis. MEG3 was upregulated in NOA tissues and inhibited cell proliferation and promoted cell Autophagy and Apoptosis in vitro. Through RNA immunoprecipitation (RIP), biotin pull-down assays, and dual-luciferase reporter assays, MEG3 was proved to act as a competing endogenous RNA of MicroRNA (miR)-21 and thus influenced the SPRY1/ERK/mTOR signaling pathway. Additionally, bioinformatic prediction and chip assay revealed that MEG3 was possibly regulated by nuclear factor κB (NF-κB) and SPRY1/NF-κB/MEG3 formed a feedback loop. Seminiferous tubule microinjection further investigated the effects of MEG3 on testes in vivo. These findings demonstrated that MEG3-miR-21-SPRY1-NF-κB probably acted as a feedback loop leading to azoospermia. Our study might provide a target and theoretical basis for diagnosing and treating NOA.

Keywords
Cell biology; Molecular biology.
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