ELABELA作为妊娠并发症的标志-综述

Q4 Biochemistry, Genetics and Molecular Biology
Rafał Sibiak
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引用次数: 0

摘要

脂肪组织分泌数十种生物活性分子,称为脂肪因子或脂肪细胞因子。Apelin受体早期内源性配体(ELABELA,也称为ELA或APELA)是胎盘组织中表达的一种与Apelin受体结合的循环信号蛋白。第一个动物实验结果表明,ELABELA缺乏可能是导致子痫前期样症状(即小鼠高血压和蛋白尿)的发病机制。外源性ELABELA补充可恢复小鼠子痫前期症状并使胎儿出生体重正常化。几项体外研究证实,补充ELABELA可以改善滋养细胞的功能,如侵袭性和增殖能力。因此,ELABELA轴可以作为妊娠并发症创新治疗的靶点。尽管如此,大多数人体研究并不支持妊娠早期ELABELA分泌紊乱与子痫前期风险增加相关的观点。因此,ELABELA不太可能作为人类先兆子痫的一种新的早期标志物。在其他妊娠并发症(如GDM和胎儿生长受限)患者中也发现了ELABELA分泌的改变。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
ELABELA as a Marker of Gestational Complications – A Review
Abstract Adipose tissue secretes dozens of biologically active molecules known as adipokines or adipocytokines. Apelin receptor early endogenous ligand (ELABELA, also known as ELA or APELA) is a circulating signaling protein expressed in placental tissue that binds to apelin receptors. The first animal experimental findings suggested that the ELABELA deficiency might be responsible for the pathogenesis of preeclampsia--like symptoms, i.e., hypertension and proteinuria in mice. Exogenous ELABELA supplementation reverted preeclampsia symptoms and normalized fetal birth weight in mice. Several in vitro studies confirmed that ELABELA supplementation could improve trophoblast cell functions such as invasiveness and proliferation capacity. Thus, the ELABELA axis could serve as the target of innovative therapies for gestational complications. Nonetheless, most human studies do not support the thesis that disturbances in ELABELA secretion in early pregnancy are associated with an increased risk of preeclampsia. Therefore, it is unlikely that ELABELA could serve as a novel early marker of preeclampsia in humans. Alterations in the ELABELA secretion have also been discovered among patients with other gestational complications such as GDM and fetal growth restriction.
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来源期刊
Medical Journal of Cell Biology
Medical Journal of Cell Biology Biochemistry, Genetics and Molecular Biology-Cell Biology
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