Structural and metabolic cumulus cell alteration affects oocyte quality in underweight women.
Hong JiQing ZhangLu DingRongjuan ChenFu LiuPing LiPublished in: Zygote (Cambridge, England) (2023)
This study aimed to investigate the structural and metabolic changes in cumulus cells of underweight women and their effects on oocyte maturation and fertilization. The cytoplasmic ultrastructure was analyzed by electron microscopy, mitochondrial membrane potential by immunofluorescence, and mitochondrial DNA copy number by relative quantitative polymerase chain reaction. The expression of various proteins including the oxidative stress-derived product 4-hydroxynonenal (4-HNE) and autophagy and apoptosis markers such as Vps34, Atg-5, Beclin 1, Lc3-I, II, Bax, and Bcl-2 was assessed and compared between groups. Oocyte maturation and fertilization rates were lower in underweight women ( P < 0.05), who presented with cumulus cells showing abnormal mitochondrial morphology and increased cell autophagy. Compared with the mitochondrial DNA copies of the control group, those of the underweight group increased but not significantly. The mitochondrial membrane potential was similar between the groups ( P = 0.8). Vps34, Atg-5, Lc3-II, Bax, and Bcl-2 expression and 4-HNE levels were higher in the underweight group compared with the control group ( P < 0.01); however, the Bax/Bcl-2 ratio was lower in the underweight group compared with the control group ( P = 0.031). Additionally, Beclin 1 protein levels were higher in the underweight group compared with the control group but without statistical significance. In conclusion, malnutrition and other conditions in underweight women may adversely affect ovulation, and the development, and fertilization of oocytes resulting from changes to the intracellular structure of cumulus cells and metabolic processes. These changes may lead to reduced fertility or unsatisfactory reproduction outcomes in women.
Keyphrases
- mitochondrial dna
- induced apoptosis
- oxidative stress
- copy number
- endoplasmic reticulum stress
- polycystic ovary syndrome
- cell cycle arrest
- signaling pathway
- cell death
- pregnancy outcomes
- poor prognosis
- stem cells
- dna damage
- mass spectrometry
- diabetic rats
- ischemia reperfusion injury
- type diabetes
- genome wide
- single cell
- cervical cancer screening
- adipose tissue
- high resolution
- cell therapy
- breast cancer risk
- binding protein
- dna methylation
- mesenchymal stem cells
- bone marrow
- small molecule
- simultaneous determination
- metabolic syndrome
- weight loss
- long non coding rna