天津医药 ›› 2026, Vol. 54 ›› Issue (2): 132-138.doi: 10.11958/20252366

• 专题研究·生殖系统疾病 • 上一篇    下一篇

糖脂互作在卵母细胞与胚胎发育中的研究进展

朱琳1,2(), 张雪玲1,2, 吴纭祺1,2, 史若锦1,2, 范勇1,2,3,4, 金龙1,2,3,4,()   

  1. 1 广州医科大学附属第三医院妇产科(邮编510150)
    2 广东省产科重大疾病重点实验室
    3 广东省妇产疾病临床医学研究中心
    4 粤港澳母胎医学高校联合实验室
  • 收稿日期:2025-06-26 修回日期:2025-08-24 出版日期:2026-02-15 发布日期:2026-02-12
  • 通讯作者: 金龙 E-mail:154540991@qq.com;kinglonvip@hotmail.com
  • 作者简介:朱琳(1995),女,硕士在读,主要从事卵母细胞成熟与胚胎发育方面研究。E-mail:154540991@qq.com
  • 基金资助:
    国家重点研发计划重点专项(2024YFC2706604)

Research progress in understanding glycolipid interactions during oocyte and embryo development

ZHU Lin1,2(), ZHANG Xueling1,2, WU Yunqi1,2, SHI Ruojin1,2, FAN Yong1,2,3,4, JIN Long1,2,3,4,()   

  1. 1 Department of Obstetrics and Gynecology, the Third Affiliated Hospital, Guangzhou Medical University, Guangzhou 510150, China
    2 Guangdong Provincial Key Laboratory of Major Obstetric Diseases
    3 Guangdong Provincial Clinical ResearchCenter for Obstetrics and Gynecology
    4 Guangdong-Hong Kong-Macao Greater Bay Area Higher Education Joint Laboratory of Maternal-Fetal Medicine
  • Received:2025-06-26 Revised:2025-08-24 Published:2026-02-15 Online:2026-02-12
  • Contact: JIN Long E-mail:154540991@qq.com;kinglonvip@hotmail.com

摘要:

代谢重编程是驱动卵母细胞成熟与早期胚胎发育的核心事件,其成败直接决定了女性生殖潜能与辅助生殖技术(ART)的结局。该文聚焦于此过程中糖与脂两大代谢轴的动态调控。卵母细胞阶段,代谢状态相对静默,依赖颗粒细胞供给的丙酮酸维持生存,并通过磷酸戊糖途径与己糖胺生物合成途径积累抗氧化物质和信号分子,为未来的发育做好准备。合子基因组激活后,胚胎发生代谢重编程,能量来源转向以葡萄糖为主导,糖酵解与脂质合成显著上调,以满足快速增殖和谱系分化的能量与生物合成需求。糖脂代谢通过共享底物和整合信号通路,共同构成了驱动这场重编程并调控细胞命运决定的核心网络。该文系统阐述了这一重编程过程中的关键代谢通路及其互作机制,并指出未来的突破口在于结合多组学分析、同位素示踪及对关键节点的靶向干预,以系统性地揭示代谢重编程的调控逻辑,为开发主动调控胚胎发育潜能的新策略、提升ART成功率奠定理论基础。

关键词: 卵母细胞, 胚胎和胎儿发育, 葡萄糖, 脂类代谢, 生殖技术,辅助

Abstract:

Metabolic reprogramming is a pivotal event driving oocyte maturation and early embryonic development, the success of which directly determines female reproductive potential and the outcomes of assisted reproductive technology (ART). This review focuses on the dynamic regulation of the glucose and lipid metabolic axes during this transition. In the oocyte stage, the metabolic state is relatively quiescent, relying on cumulus cell-supplied pyruvate for survival. Concurrently, the pentose phosphate pathway and hexosamine biosynthetic pathway are utilized to accumulate antioxidants and signaling molecules, thereby preparing the oocyte for future developmental competence. Following zygotic genome activation (ZGA), the embryo initiates metabolic reprogramming. The primary energy source shifts to glucose, with significant upregulation of glycolysis and lipid synthesis to meet the bioenergetic and biosynthetic demands of rapid proliferation and lineage specification. The interplay between glucose and lipid metabolism,through shared substrates and integrated signaling pathways, constitutes the core network that drives this reprogramming and governs cell fate decisions. This article systematically elucidates the key metabolic pathways and their interaction mechanisms. We propose that future breakthroughs will emerge from combining multi-omics analyses, isotope tracing and targeted interventions at critical nodes to systematically uncover the regulatory logic of metabolic reprogramming. Such efforts will establish a theoretical foundation for developing novel strategies to actively modulate embryonic developmental potential and enhance ART success rates.

Key words: oocytes, embryonic and fetal development, glucose, lipid metabolism, reproductive techniques, assisted

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