OONO-/MMP2/MMP9 pathway-mediated apoptosis of porcine granulosa cells is associated with DNA damage.
Kun LeiQuanwei WeiYing ChengZhe WangHaoze WuFang ZhaoWei DingFangxiong ShiPublished in: Reproduction (Cambridge, England) (2023)
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.
Keyphrases
- dna damage
- oxidative stress
- induced apoptosis
- dna repair
- cell migration
- endoplasmic reticulum stress
- poor prognosis
- nitric oxide
- signaling pathway
- cell death
- computed tomography
- type diabetes
- magnetic resonance imaging
- magnetic resonance
- mass spectrometry
- binding protein
- dna damage response
- hydrogen peroxide
- heat stress
- dna binding
- liquid chromatography