妊娠晚期滋养细胞干细胞功能受损,胎儿生长受限。

IF 3.5 3区 生物学 Q3 CELL BIOLOGY
Cherry Sun , Teena KJB. Gamage , Jasper Perry , Vicky Fan , Lawrence W. Chamley , Joanna L. James
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引用次数: 0

摘要

滋养细胞是对胎盘发育和功能至关重要的上皮细胞,确保胎儿的健康生长。我们之前已经使用侧群技术从妊娠早期胎盘中分离出滋养细胞干细胞(TSC),结果表明它们首次持续存在至足月,并在胎儿生长受限(FGR)中耗尽——胎儿生长受限是胎盘交换功能受损的一种严重妊娠状况。然而,TSC在妊娠病理中的功能作用尚未被直接研究。在这里,我们首先证明妊娠晚期的侧群滋养细胞代表了一个TSC群体,可以以与妊娠早期相似的方式分化为成熟的滋养细胞谱系,然后结合转录组学和功能研究来证明FGR中增殖、分化和细胞死亡易感的缺陷。总之,这种干细胞水平的缺陷可能对所有下游滋养细胞谱系产生深远的影响,这可能解释了FGR中胎盘受损的原因。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Third-trimester trophoblast stem cell function is impaired in fetal growth restriction
Trophoblasts are epithelial cells critical for placental development and function, ensuring healthy fetal growth. We have previously isolated trophoblast stem cells (TSC) from first trimester placentae using the side-population technique, showing that they persist to term for the first time, and are depleted in fetal growth restriction (FGR) – a serious condition of pregnancy where placental exchange function is impaired. However, the functional role of TSC in pregnancy pathologies has not previously been directly examined. Here, we first demonstrate that third-trimester side-population trophoblasts represent a TSC population that can differentiate into mature trophoblast lineages in a similar manner to their first trimester counterparts, and then combine transcriptomic and functional studies to demonstrate deficits in proliferation, differentiation, and susceptibility to cell death in FGR. Together, such stem cell level defects may have profound impacts on all downstream trophoblast lineages, potentially explaining why placentation is impaired in FGR.
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来源期刊
Experimental cell research
Experimental cell research 医学-细胞生物学
CiteScore
7.20
自引率
0.00%
发文量
295
审稿时长
30 days
期刊介绍: Our scope includes but is not limited to areas such as: Chromosome biology; Chromatin and epigenetics; DNA repair; Gene regulation; Nuclear import-export; RNA processing; Non-coding RNAs; Organelle biology; The cytoskeleton; Intracellular trafficking; Cell-cell and cell-matrix interactions; Cell motility and migration; Cell proliferation; Cellular differentiation; Signal transduction; Programmed cell death.
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