Embryo Biotechnology and Reproduction Laboratory, Institute of Animal Sciences, Chinese Academy of Agricultural Sciences, Beijing 100193, China.
Int J Mol Sci. 2022 Oct 30;23(21):13222. doi: 10.3390/ijms232113222.
This study aims to investigate the effects of CLAUDIN-6 (CLDN6) on cell apoptosis and proliferation of bovine cumulus cells (CCs). Immunofluorescence staining was used to localize CLDN6 protein in CCs. Three pairs of siRNA targeting CLDN6 and one pair of siRNA universal negative sequence as control were transfected into bovine CCs. Then, the effective siRNA was screened by real-time quantitative PCR (RT-qPCR) and Western blotting. The mRNA expression levels of apoptosis related genes (CASPASE-3, BAX and BCL-2) and proliferation related genes (PCNA, CDC42 and CCND2) were evaluated by RT-qPCR in CCs with CLDN6 knockdown. Cell proliferation, apoptosis and cell cycle were detected by flow cytometry with CCK-8 staining, Annexin V-FITC staining and propidium iodide staining, respectively. Results showed that the CLDN6 gene was expressed in bovine CCs and the protein was localized in cell membranes and cytoplasms. After CLDN6 was knocked down in CCs, the cell apoptosis rate significantly decreased and the pro-apoptotic genes BAX and CASPASE-3 were down-regulated significantly, whereas the anti-apoptotic gene BCL-2 was markedly up-regulated (p < 0.05). Additionally, CLDN6 knockdown significantly enhanced cell proliferation of CCs at 72 h after siRNA transfection. The mRNA levels of proliferation-related genes PCNA, CCND2 and CDC42 increased obviously in CCs with CLDN6 knockdown (p < 0.05). After CLDN6 was down-regulated, the percentage of CCs at S phase was significantly increased (p < 0.05). However, there was no remarkable difference in the percentages of cells at the G0/G1 phase and G2/M phase between CCs with or without CLDN6 knockdown (p > 0.05). Therefore, the expression of CLDN6 and its effects on cell proliferation, apoptosis and cell cycle of bovine CCs were first studied. CLDN6 low expression inhibited cell apoptosis, induced cell proliferation and cell cycle arrest of bovine CCs.
本研究旨在探讨 Claudin-6 (CLDN6) 对牛卵丘细胞 (CCs) 凋亡和增殖的影响。免疫荧光染色用于定位 CCs 中的 CLDN6 蛋白。针对 CLDN6 的三对 siRNA 和一对作为对照的通用负序列 siRNA 被转染到牛 CCs 中。然后,通过实时定量 PCR (RT-qPCR) 和 Western 印迹筛选有效 siRNA。用 CLDN6 敲低的 CCs 评估凋亡相关基因 (CASPASE-3、BAX 和 BCL-2) 和增殖相关基因 (PCNA、CDC42 和 CCND2) 的 mRNA 表达水平。用 CCK-8 染色、Annexin V-FITC 染色和碘化丙啶染色分别通过流式细胞术检测细胞增殖、凋亡和细胞周期。结果表明,CLDN6 基因在牛 CCs 中表达,蛋白定位于细胞膜和细胞质。CCs 中的 CLDN6 敲低后,细胞凋亡率显著降低,促凋亡基因 BAX 和 CASPASE-3 显著下调,而抗凋亡基因 BCL-2 明显上调 (p<0.05)。此外,CLDN6 敲低后,siRNA 转染 72 小时后 CCs 的增殖明显增强。CCs 中 CLDN6 敲低后增殖相关基因 PCNA、CCND2 和 CDC42 的 mRNA 水平明显升高 (p<0.05)。CLDN6 下调后,CCs 处于 S 期的比例显著增加 (p<0.05)。然而,CCs 中处于 G0/G1 期和 G2/M 期的细胞比例在有无 CLDN6 敲低之间没有显著差异 (p>0.05)。因此,首次研究了 CLDN6 的表达及其对牛 CCs 增殖、凋亡和细胞周期的影响。CLDN6 低表达抑制细胞凋亡,诱导牛 CCs 增殖和细胞周期停滞。