Hypoxia-inducible factors (HIFs) in early pregnancy: implications for miscarriage†.

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC
Yuxuan Lai, Zhiyu Fu, Yaxin Gao, Ning Ma, Lu Li
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引用次数: 0

Abstract

Miscarriage poses a significant threat to both maternal and fetal health. Its etiology remains unknown, and there are no established effective identification or prevention strategies. A low-oxygen environment in early pregnancy is a physiological necessity for embryonic and placental growth. Hypoxia-inducible factors are a family of classic hypoxia signaling molecules whose expression level may fluctuate abnormally because of an imbalance in oxygen levels. Its unusual fluctuations initiate multiple signaling pathways at the maternal womb. Hypoxia-inducible factors are a family of classic hypoxia-signaling molecules and immune tolerance. Notably, aberrant regulation of these processes may lead to miscarriage. This review aims to clarify how the hypoxia-inducible factor-1α mediates the aberrant regulation of biological processes, including autophagy, metabolic reprogramming, et al., and how these effects impact trophoblasts and other cells at the maternal-fetal interface. These findings provide new insights into potential therapeutic and preventive strategies for miscarriage.

妊娠早期的低氧诱导因子(HIFs):对流产的影响†。
流产对孕产妇和胎儿的健康都构成重大威胁。流产的病因至今不明,也没有有效的识别或预防策略。妊娠早期的低氧环境是胚胎和胎盘生长的生理需要。缺氧诱导因子(HIFs)是典型的缺氧信号分子家族,其表达水平会因氧气水平失衡而异常波动。其异常波动会在母胎界面启动多种信号通路,并调节一系列表型变化,包括增殖、分化、迁移、侵袭、血管生成、子宫内膜蜕膜化和免疫耐受。值得注意的是,这些过程的异常调控可能会导致流产。本综述旨在阐明 HIF-1α 如何介导自噬、代谢重编程、免疫、表观遗传学和血管生成等生物过程的异常调控,以及这些效应如何影响滋养细胞和母胎界面的其他细胞。这些发现为流产的潜在治疗和预防策略提供了新的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
7.20
自引率
4.30%
发文量
567
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