The proliferation and differentiation of spermatogonial stem cells in the frist wave of spermatogenesis in rats with Trib3 gene knockout

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS ACS Applied Bio Materials Pub Date : 2024-07-03 DOI:10.1016/j.repbio.2024.100921
Jie Bai , Xia Yun , Xuguang Xu , Shanshan Liu , Sidegeer Zhang , Taodi Liu , Yan Zhang
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Abstract

This study explores the effects of Trib3 gene knockout on adult male rat spermatogenesis. Using CRISPR/Cas9, we knocked out the Trib3 gene in Wistar rats. Results indicate altered expression of PLZF, ID4, and c-KIT in knockout rats, suggesting impaired spermatogonial stem cell proliferation and differentiation. Histological analysis reveals reduced seminiferous tubule area and decreased spermatocyte numbers. Mating experiments demonstrate reduced offspring rates after the second self-mating in knockout rats. SYCP3, a meiosis marker, shows elevated expression in knockout rat testes at 14 days postpartum, suggesting an impact on reproductive processes. ELISA results indicate decreased testosterone, FSH, and FGF9 levels in knockout rat testicular tissues. In conclusion, Trib3 gene deletion may impede spermatogonial self-renewal and promote differentiation through the FSH-FGF9- c-KIT interaction and p38MAPK pathway, affecting reproductive capacity. These findings contribute to understanding the molecular mechanisms regulating spermatogenesis.

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Trib3基因敲除大鼠精子发生第一阶段精原干细胞的增殖与分化
本研究探讨了敲除 Trib3 基因对成年雄性大鼠精子发生的影响。我们利用 CRISPR/Cas9 技术敲除了 Wistar 大鼠的 Trib3 基因。结果表明,基因敲除大鼠体内 PLZF、ID4 和 c-KIT 的表达发生了改变,这表明精原干细胞的增殖和分化能力受损。组织学分析显示,曲细精管面积缩小,精母细胞数量减少。交配实验表明,基因敲除大鼠第二次自我交配后的后代率降低。SYCP3是一种减数分裂标记物,在产后14天,基因敲除大鼠睾丸中的SYCP3表达量升高,表明其对生殖过程有影响。酶联免疫吸附试验结果表明,基因敲除大鼠睾丸组织中的睾酮、前列腺素和前列腺生长因子9水平下降。总之,Trib3 基因缺失可能会阻碍精原细胞自我更新,并通过 FSH-FGF9- c-KIT 相互作用和 p38MAPK 通路促进分化,从而影响生殖能力。这些发现有助于了解精子发生的分子调控机制。
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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
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