HucMSC-EVs Facilitate In Vitro Development of Maternally Aged Preantral Follicles and Oocytes.
Ying-Yi ZhangWeijie YangYi ZhangZhanhong HuYingyan ChenYerong MaAnran YangZhan ShiHanjing ZhouPeipei RenLibing ShiJiamin JinYan RongXiaomei TongYin-Li ZhangSong-Ying ZhangPublished in: Stem cell reviews and reports (2023)
Follicle developmental capacity and oocyte quality decline with advanced maternal age. Extracellular vesicles from human umbilical cord mesenchymal stem cells (HucMSC-EVs) act as a potential therapeutic product in the treatment of age-related ovarian dysfunction. In vitro culture (IVC) of preantral follicles is a useful method for understanding the mechanism of follicle development and is a promising means for improving female fertility. However, whether HucMSC-EVs have beneficial effects on aged follicle development during IVC has not yet been reported. Our research demonstrated that follicular development with single-addition withdrawal of HucMSC-EVs was better than that with continuous treatment with HucMSC-EVs. HucMSC-EVs facilitated the survival and growth of follicles, promoted the proliferation of granulosa cells (GCs), and improved the steroid hormone secretion of GCs during IVC of aged follicles. Both GCs and oocytes could uptake HucMSC-EVs. Moreover, we observed elevated cellular transcription in GCs and oocytes after treatment with HucMSC-EVs. The RNA sequencing (RNA-seq) results further validated that the differentially expressed genes are related to the promotion of GC proliferation, cell communication, and oocyte spindle organization. Additionally, the aged oocytes displayed a higher maturation rate, presented less aberrant spindle morphology, and expressed a higher level of the antioxidant protein Sirtuin 1 (SIRT1) after treatment with HucMSC-EVs. Our findings suggested that HucMSC-EVs can improve the growth and quality of aged follicles and oocytes in vitro through the regulation of gene transcription, which provides evidence for HucMSC-EVs as potential therapeutic reagents to restore female fertility with advanced age.
Keyphrases
- mesenchymal stem cells
- umbilical cord
- single cell
- rna seq
- oxidative stress
- inferior vena cava
- endothelial cells
- genome wide
- gene expression
- pregnant women
- bone marrow
- type diabetes
- dna methylation
- transcription factor
- metabolic syndrome
- induced apoptosis
- cell therapy
- combination therapy
- pulmonary embolism
- quality improvement
- weight loss
- protein protein
- weight gain
- small molecule
- amino acid
- liquid chromatography
- birth weight
- genome wide identification
- free survival
- childhood cancer