C-X-C motif chemokine ligand 12 improves the developmental potential of bovine oocytes by activating SH2 domain-containing tyrosine phosphatase 2 during maturation

In vitro maturation of mammalian oocytes is an important means in assisted reproductive technology. Most bovine immature oocytes complete nuclear maturation, but less than half develop to the blastocyst stage after fertilization. Thus, inefficient in vitro production is mainly caused by a suboptimal...

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Veröffentlicht in:Biology of reproduction 2023-09, Vol.109 (3), p.282-296
Hauptverfasser: Zhang, Min, Zhang, Jingcheng, Wang, Debao, Liu, Zhengqing, Xing, Kangning, Wang, Yongsheng, Jiao, Mei, Wang, Yong, Shi, Binqiang, Zhang, Hexu, Zhang, Yong
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Sprache:eng
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Zusammenfassung:In vitro maturation of mammalian oocytes is an important means in assisted reproductive technology. Most bovine immature oocytes complete nuclear maturation, but less than half develop to the blastocyst stage after fertilization. Thus, inefficient in vitro production is mainly caused by a suboptimal in vitro culture process, in which oocyte quality appears to be the limiting factor. In our study, a potential maternal regulator, C-XC motif chemokine ligand 12, was identified by analyzing transcriptome data. C-X-C motif chemokine ligand 12 supplementation promoted the developmental potential of oocytes by improving protein synthesis and reorganizing cortical granules and mitochondria during in vitro maturation, which eventually increased blastocyst formation efficiency and cell number after parthenogenesis, fertilization, and cloning. All these promoting effects by C-X-C motif chemokine ligand 12 were achieved by activating SH2 domain-containing tyrosine phosphatase 2, thereby promoting the mitogen-activated protein kinase signaling pathway. These findings provide an in vitro maturation system that closely resembles the maternal environment to provide high-quality oocytes for in vitro production. Summary Sentence CXCL12 improves the developmental potential of bovine oocytes by activating SHP2 during maturation. Graphical Abstract
ISSN:0006-3363
1529-7268
1529-7268
DOI:10.1093/biolre/ioad079