College of Animal Science and Technology, Nanjing Agricultural University, Nanjing, China.
Institute of Animal Science, Jiangsu Academy of Agricultural Sciences, Nanjing, China.
Reproduction. 2023 Mar 15;165(4):431-443. doi: 10.1530/REP-22-0295. Print 2023 Apr 1.
The apoptosis of granulosa cells (GCs) is the main reason for porcine follicular atresia. This study provides a novel mechanism for peroxynitrite anion-mediated GC apoptosis and follicular atresia in porcine ovary.
Granulosa cells play a crucial role in the development of follicles, and their cell apoptosis in the porcine ovary is a major contributor to follicular atresia. Here, we provide a new mechanism for follicular atresia by describing a crucial mechanism by which peroxynitrite anion (OONO-) may cause GC death. We discovered that nitric oxide, oxidative stress level, and OONO- were positively correlated with porcine follicular atresia, which was accompanied by high expression of matrix metalloproteinase 2 (MMP2) and MMP9. We created a model of OONO--induced apoptosis in GCs and discovered that OONO- could boost the expression of MMP2 and MMP9 and increase the expression of pro-apoptotic proteins and DNA damage. Furthermore, by inhibiting the activities of MMP2 and MMP9, we found that SB-3CT (a specific inhibitor for MMP2 and MMP9) alleviated the decrease in cell survival rates and DNA damage caused by OONO-, which may have been impacted by reducing the cleavage of PARP1 by MMP2 and MMP9. Therefore, our findings imply that OONO- can cause DNA damage to GCs, participating in mediating the expression of pro-apoptotic proteins and inhibiting DNA repair by preventing the activity of PARP1 through MMP2 and MMP9. These results help explain how OONO-/MMP2/MMP9 affects porcine follicular atresia and GC apoptosis.
颗粒细胞(GCs)的凋亡是猪卵泡闭锁的主要原因。本研究为过氧亚硝酸盐阴离子介导的猪卵巢 GC 凋亡和卵泡闭锁提供了新的机制。
颗粒细胞在卵泡发育中起关键作用,其在猪卵巢中的细胞凋亡是卵泡闭锁的主要原因。在这里,我们通过描述过氧亚硝酸盐阴离子(OONO-)可能导致 GC 死亡的关键机制,提供了一种新的卵泡闭锁机制。我们发现一氧化氮、氧化应激水平和 OONO-与猪卵泡闭锁呈正相关,同时伴随着基质金属蛋白酶 2(MMP2)和 MMP9 的高表达。我们创建了一个 OONO-诱导 GCs 凋亡的模型,发现 OONO-可以上调 MMP2 和 MMP9 的表达,并增加促凋亡蛋白和 DNA 损伤的表达。此外,通过抑制 MMP2 和 MMP9 的活性,我们发现 SB-3CT(MMP2 和 MMP9 的特异性抑制剂)减轻了 OONO-引起的细胞存活率和 DNA 损伤的降低,这可能是通过减少 MMP2 和 MMP9 对 PARP1 的切割来实现的。因此,我们的研究结果表明,OONO-可以对 GCs 造成 DNA 损伤,通过 MMP2 和 MMP9 抑制 PARP1 的活性,参与介导促凋亡蛋白的表达和抑制 DNA 修复。这些结果有助于解释 OONO-/MMP2/MMP9 如何影响猪卵泡闭锁和 GC 凋亡。