Follicle Biology Laboratory (FOBI), Vrije Universiteit Brussel (VUB) Jette Campus, Laarbeeklaan 103, 1090, Brussels, Belgium.
Laboratory of Cellular Biochemistry, Department of Biochemistry, ICBS, Federal University of Rio Grande do Sul (UFRGS), (RS), Porto Alegre, 90035003, Brazil.
J Assist Reprod Genet. 2023 Dec;40(12):2851-2863. doi: 10.1007/s10815-023-02940-7. Epub 2023 Sep 30.
Glucose and redox metabolism characterization in mouse antral follicles with meiotically blocked oocytes, after in vitro follicle culture (IFC) from the early secondary stage.
Following IFC (10 days), oocytes, corresponding cumulus (CC), and granulosa cells (GC) were collected from antral follicles: (i) on day 9-immature, germinal vesicle (GV) stage; (ii) on day 10, after hCG/EGF stimulation-mature, metaphase II (MII) stage and meiotically blocked (MB) immature GV stage. The metabolic profiles of all samples (GV, MII, and MB) were compared by measuring changes in metabolites involved in glycolysis, tricarboxylic acid (TCA) cycle, pentose phosphate pathway (PPP), and redox activity via enzymatic spectrophotometric assays in each cell type.
Within MB follicles, GCs drive higher levels of glycolysis and lactic acid fermentation (LAF) while oocytes exert more PPP activity. MB-oocytes had significantly larger diameters compared to day 9 GVs. MB follicles revealed limited metabolic changes in the somatic compartment compared to their GV counterparts (before stimulation). MB-CCs showed increased aconitase and glucose-6-phosphate dehydrogenase activities with lower malate levels comparted to GV-CCs. MB and MII in vitro grown follicles displayed comparable metabolic profiles, suggesting culture induces metabolic exhaustion regardless of the maturation stage.
Current results suggest that in addition to impaired nuclear maturation, metabolic disruption is present in MB follicles. MB follicles either compensate with high levels of TCA cycle and PPP activities in CCs, or are unable to drive proper levels of aerobic metabolism, which might be due to the current culture conditions.
在体外卵泡培养(IFC)从早期次级阶段后,研究减数分裂阻断卵母细胞的小鼠腔前卵泡的葡萄糖和氧化还原代谢特征。
在 IFC(10 天)后,从腔前卵泡中收集卵母细胞、相应的卵丘(CC)和颗粒细胞(GC):(i)第 9 天-未成熟,生发泡(GV)阶段;(ii)第 10 天,在 hCG/EGF 刺激后-成熟,中期 II(MII)阶段和减数分裂阻断(MB)未成熟 GV 阶段。通过测量参与糖酵解、三羧酸(TCA)循环、磷酸戊糖途径(PPP)和每个细胞类型中还原活性的代谢物变化,比较所有样品(GV、MII 和 MB)的代谢谱。
在 MB 卵泡中,GC 驱动更高水平的糖酵解和乳酸发酵(LAF),而卵母细胞发挥更多的 PPP 活性。MB 卵母细胞的直径明显大于第 9 天的 GV。与 GV 对应物(刺激前)相比,MB 卵泡的体细胞区室显示出有限的代谢变化。MB-CCs 显示出增加的乌头酸酶和葡萄糖-6-磷酸脱氢酶活性,以及与 GV-CCs 相比更低的苹果酸水平。MB 和体外生长的 MII 卵泡显示出可比的代谢谱,表明培养诱导代谢衰竭,无论成熟阶段如何。
目前的结果表明,除了核成熟受损外,MB 卵泡中还存在代谢紊乱。MB 卵泡要么通过 CCs 中高水平的 TCA 循环和 PPP 活性来代偿,要么无法驱动适当水平的需氧代谢,这可能是由于目前的培养条件所致。