Role of p57KIP2 in Stem and Progenitor Leydig Cells of Mouse Testes.

IF 4 3区 医学 Q1 ANDROLOGY World Journal of Mens Health Pub Date : 2024-04-12 DOI:10.5534/wjmh.230299
Seung Hyun Park, Kyung Noh Yoon, Yang Xu, Myung Chan Gye
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引用次数: 0

Abstract

Purpose: Precise control of proliferation and differentiation of Leydig cells is important for gonadal androgenesis and spermatogenesis. Though cyclin-dependent kinase inhibitors are crucial for cell proliferation and differentiation, their role in the development of early adult Leydig cells (ALCs) remained unanswered. To understand mechanism for ALC development, functional expression of p57KIP2 (cdkn1c) was investigated in the stem Leydig cells (SLCs) and progenitor Leydig cells (PLCs) in mice.

Materials and methods: The roles of p57KIP2 in the proliferation, differentiation, apoptosis, and steroidogenesis in SLCs and PLCs were investigated by antibodies and bromodeoxyuridine (BrdU) labeling in the early neonatal testes and p57kip2 siRNA in the isolated SLCs and PLCs. Steroidogenic differentiation of PLCs was examined by progesterone and testosterone production in cell culture.

Results: From postnatal day (PND) 1 to 14, p57KIP2(+) spindle-shaped cells in the testis interstitium were α-smooth muscle actin (αSMA)(-), a peritubular myoid cells marker, suggesting that they are SLCs and PLCs. Besides, p57KIP2 was also expressed in HSD3β(+) fetal Leydig cells. From PND1 to 14, BrdU(+)/αSMA(-), Ki67(+)/p57KIP2(+), and BrdU(+)/p57KIP2(+) spindle-shaped cells were gradually decreased. From PND1 to 14, p57KIP in the αSMA(-)/p57KIP2(+) cells was peaked at PND7 and decreased thereafter. In THY1(+) isolated SLCs, p57kip2 siRNA significantly increased ki67 and pcna mRNA and pdgfrα mRNA, a differentiation marker and decreased nestin mRNA, a SLC marker. No significant difference in apoptosis related genes mRNA was found after p57kip2 siRNA treatment. In HSD3β(+) PLCs, p57kip2 siRNA increased proapoptotic genes mRNA, annexin V(+) early-apoptotic cells. Importantly, p57kip2 siRNA significantly decreased hsd3β6 and cyp17a1 mRNA and progesterone production.

Conclusions: p57KIP2 may suppress proliferation and support stemness of SLCs. In PLCs, p57KIP2 may suppress apoptosis and potentiate the steroidogenic differentiation.

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p57KIP2 在小鼠睾丸的干细胞和原生精原细胞中的作用
目的:精确控制 Leydig 细胞的增殖和分化对性腺雄激素生成和精子发生非常重要。尽管细胞周期蛋白依赖性激酶抑制剂对细胞的增殖和分化至关重要,但它们在早期成体雷迪格细胞(ALC)发育过程中的作用仍未得到解答。为了了解ALC的发育机制,研究人员调查了p57KIP2(cdkn1c)在小鼠干Leydig细胞(SLCs)和祖Leydig细胞(PLCs)中的功能表达:用抗体和溴脱氧尿苷(BrdU)标记新生小鼠早期睾丸,用p57kip2 siRNA标记分离的SLCs和PLCs,研究p57KIP2在SLCs和PLCs的增殖、分化、凋亡和类固醇生成过程中的作用。通过在细胞培养中产生黄体酮和睾酮检验了PLC的类固醇分化情况:结果:从出生后第1天到第14天,睾丸间质中的p57KIP2(+)纺锤形细胞均为α-平滑肌肌动蛋白(αSMA)(-),而α-平滑肌肌动蛋白(αSMA)是睾丸周围肌细胞的标记,这表明它们是SLCs和PLCs。此外,p57KIP2也在HSD3β(+)胎儿Leydig细胞中表达。从PND1到14,BrdU(+)/αSMA(-)、Ki67(+)/p57KIP2(+)和BrdU(+)/p57KIP2(+)纺锤形细胞逐渐减少。从 PND1 到 14,αSMA(-)/p57KIP2(+)细胞中的 p57KIP 在 PND7 达到峰值,之后逐渐下降。在THY1(+)分离的SLC中,p57kip2 siRNA能显著增加ki67和pcna mRNA以及分化标志物pdgfrα mRNA,并降低SLC标志物nestin mRNA。p57kip2 siRNA处理后,凋亡相关基因mRNA无明显差异。在 HSD3β(+) PLCs 中,p57kip2 siRNA 增加了促凋亡基因 mRNA、annexin V(+) 早期凋亡细胞。重要的是,p57kip2 siRNA能显著降低hsd3β6和cyp17a1 mRNA及孕酮的产生。结论:p57KIP2可抑制SLCs的增殖并支持其干性,在PLCs中,p57KIP2可抑制凋亡并促进类固醇生成分化。
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来源期刊
World Journal of Mens Health
World Journal of Mens Health Medicine-Psychiatry and Mental Health
CiteScore
7.60
自引率
2.10%
发文量
92
审稿时长
6 weeks
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