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干细胞在子宫复旧中的作用。

The role of stem cells in uterine involution.

作者信息

Spooner Madelyn K, Lenis Yasser Y, Watson Rachel, Jaimes Daniela, Patterson Amanda L

机构信息

Division of Animal Sciences, University of Missouri, Columbia, Missouri, USA.

Department of Animal Sciences, Faculty of Agricultural Sciences, National University of Colombia, Palmira, Colombia.

出版信息

Reproduction. 2021 Mar;161(3):R61-R77. doi: 10.1530/REP-20-0425.

Abstract

Uterine remodeling during pregnancy and repair postpartum are fundamental to the successful propagation of eutherian species. The most drastic remodeling occurs in species with invasively implanting embryos, including humans and mice. During embryo implantation, embryonic trophoblasts breach the epithelium, penetrating into the stroma. Stromal cell decidualization, which is critical for the establishment and maintenance of early pregnancy, occurs throughout the implantation site. Trophoblasts further invade into and remodel uterine spiral arteries, which is necessary for placental formation. The uterus increases in size up to 24-fold, which is largely attributed to myometrial expansion. Uterine changes that occur during pregnancy must then be resolved postpartum. Following parturition, the uterus repairs the remodeled tissue in the process of uterine involution. During involution, the majority of the endometrium is regenerated to replace the tissue that is shed postpartum. The myometrium returns to the pre-gravid state which is thought to occur through apoptosis and autophagy of smooth muscle cells. Although we understand the general process of postpartum uterine involution, the detailed mechanisms, particularly the role of putative stem cells, are poorly understood. This review discusses the evidence for the existence of epithelial, stromal and myometrial stem cells and their role in uterine involution. Gaps in knowledge and areas for future research are also considered. Studies of both postpartum and menstrual uterine repair, which likely involve similar mechanisms, are described under the broad definition of uterine involution. Although the primary focus of this review is human, mouse models are discussed to provide additional information.

摘要

孕期子宫重塑和产后修复是真兽类物种成功繁衍的基础。最剧烈的重塑发生在胚胎侵入性着床的物种中,包括人类和小鼠。在胚胎着床期间,胚胎滋养层细胞突破上皮,侵入基质。基质细胞蜕膜化在整个着床部位发生,这对早期妊娠的建立和维持至关重要。滋养层细胞进一步侵入并重塑子宫螺旋动脉,这是胎盘形成所必需的。子宫大小增加至24倍,这主要归因于子宫肌层的扩张。孕期发生的子宫变化随后必须在产后得到解决。分娩后,子宫在子宫复旧过程中修复重塑的组织。在复旧过程中,大部分子宫内膜再生以替代产后脱落的组织。子宫肌层恢复到妊娠前状态,这被认为是通过平滑肌细胞的凋亡和自噬实现的。尽管我们了解产后子宫复旧的一般过程,但详细机制,特别是假定干细胞的作用,仍知之甚少。本综述讨论了上皮、基质和子宫肌层干细胞存在的证据及其在子宫复旧中的作用。还考虑了知识空白和未来研究领域。在子宫复旧的广义定义下描述了产后和月经性子宫修复的研究,它们可能涉及相似的机制。尽管本综述的主要重点是人类,但也讨论了小鼠模型以提供更多信息。

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