Differences in transcriptomic profiles of human cumulus cells isolated from oocytes at GV, MI and MII stages after in vivo and in vitro oocyte maturation

被引:69
作者
Ouandaogo, Zamalou Gisele [1 ,2 ]
Frydman, Nelly [3 ]
Hesters, Laetitia [3 ]
Assou, Said [1 ,2 ]
Haouzi, Delphine [1 ,2 ]
Dechaud, Herve [1 ,2 ,4 ]
Frydman, Rene [3 ]
Hamamah, Samir [1 ,2 ,4 ,5 ]
机构
[1] Hop St Eloi, CHU Montpellier, Inst Res Biotherapy, F-34295 Montpellier, France
[2] INSERM, U1040, F-34295 Montpellier, France
[3] Hop Antoine Beclere, Serv Gynecol Obstet, Clamart, France
[4] Univ Montpellier I, UFR Med, F-34295 Montpellier, France
[5] Hop Arnaud Villeneuve, CHU Montpellier, Dept Biol Reduct, UAM,AMP DPI, F-34295 Montpellier 5, France
关键词
cumulus cells; DNA microarray; gene expression profile; maturation condition; GENE-EXPRESSION PROFILES; HEAT-SHOCK RESPONSE; FANCONI-ANEMIA; DEVELOPMENTAL COMPETENCE; BOVINE OOCYTES; GROWTH-FACTOR; PIG OOCYTES; LH; OVULATION; FOLLICLE;
D O I
10.1093/humrep/des172
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Oocyte maturation and competence to development depends on its close relationship with cumulus cells (CCs). However, the maturation conditions of human cumulusoocyte complexes (COCs) might affect gene expression in both oocyte and CCs. We thus compared the transcriptome profiles of CCs isolated from in vivo and in vitro matured COCs at different nuclear maturation stages. Three groups of CCs from patients who underwent ICSI were included: CCs of patients with polycystic ovary syndrome (PCOS) referred for in vitro maturation (IVM), CCs from patients with PCOS for in vivo maturation (used as controls) and CCs from normal responders referred for in vivo maturation. CCs were isolated from COCs at the germinal vesicle, metaphase I and metaphase II stages. Microarray technology was used to analyse the global gene expression and significance analysis of microarray to compare the expression profiles of CCs from COCs at different nuclear maturation stages following IVM or in vivo maturation. Selected genes were validated by RT-qPCR. In CCs isolated after IVM, genes related to cumulus expansion and oocyte maturation, such as EREG, AREG and PTX3, were down-regulated, while cell cycle-related genes were up-regulated in comparison with CCs from in vivo matured COCs from PCOS and normal responder patients. Moreover, irrespective of the stage of oocyte maturation, genes involved in DNA replication, recombination and repair were up-regulated in CCs after IVM. The CC transcriptomic signature varies according to both the oocyte maturation stage and the maturation conditions. Our findings suggest a delay in the acquisition of the mature CC phenotype following IVM, opening a new perspective for the improvement in IVM conditions.
引用
收藏
页码:2438 / 2447
页数:10
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