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胎盘的钙信号转导。

Calcium signaling in placenta.

机构信息

Research Centre for Women's and Infants' Health (RCWIH) at the Samuel Lunenfeld Research Institute of Mount Sinai Hospital, University of Toronto, Toronto, Ontario, Canada.

出版信息

Cell Calcium. 2011 May;49(5):350-6. doi: 10.1016/j.ceca.2010.12.003. Epub 2011 Jan 14.

Abstract

The placenta sustains the developing fetus throughout gestation and its major functions include nutrition, gas and waste exchange via a variety of passive or active mechanisms. Up to 30 g of calcium (Ca(2+)) actively crosses the trophoblast layer during human pregnancy. The Ca(2+) ion not only plays an important role for skeletal development but is also an essential second messenger. This review is intended to highlight the implications of Ca(2+) signaling during reproduction and specifically placentation. Initially, a Ca(2+) wave induces fertilization of the oocyte. The intracellular Ca(2+) concentration is key for the blastocyst implantation, proper placental development and function. Current knowledge of many proteins involved in placental Ca(2+) regulation and their function in pathologic conditions is largely limited. Recent studies, however, point to alterations in Ca(2+) homeostasis in placental pathologies such as pre-eclampsia (PE) and intrauterine growth restriction (IUGR). A broader understanding of the role of Ca(2+) signaling during human reproduction may offer insight into impaired pregnancy outcomes.

摘要

胎盘在整个妊娠期间为发育中的胎儿提供营养,并通过各种被动或主动机制进行气体和废物交换。在人类妊娠期间,高达 30 克的钙(Ca(2+))主动穿过滋养层。钙离子不仅对骨骼发育很重要,而且是一种必需的第二信使。本综述旨在强调 Ca(2+)信号在生殖特别是胎盘形成中的意义。最初,Ca(2+)波诱导卵子受精。细胞内 Ca(2+)浓度对于胚泡着床、胎盘的适当发育和功能非常关键。目前对许多参与胎盘 Ca(2+)调节的蛋白质及其在病理条件下的功能的了解在很大程度上受到限制。然而,最近的研究表明,子痫前期(PE)和宫内生长受限(IUGR)等胎盘病理中存在 Ca(2+)稳态的改变。更广泛地了解 Ca(2+)信号在人类生殖中的作用可能有助于深入了解受损的妊娠结局。

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