Cousins Fiona L, Filby Caitlin E, Gargett Caroline E
The Ritchie Centre, Hudson Institute of Medical Research, Clayton, VIC, Australia.
Department of Obstetrics and Gynecology, Monash University, Clayton, VIC, Australia.
Front Reprod Health. 2022 Jan 20;3:811537. doi: 10.3389/frph.2021.811537. eCollection 2021.
The human endometrium is a remarkable tissue, undergoing ~450 cycles of proliferation, differentiation, shedding (menstruation), repair, and regeneration over a woman's reproductive lifespan. Post-menstrual repair is an extremely rapid and scar-free process, with re-epithelialization of the luminal epithelium completed within 48 h of initiation of shedding. Following menstruation, the functionalis grows from the residual basalis layer during the proliferative phase under the influence of rising circulating estrogen levels. The regenerative capacity of the endometrium is attributed to stem/progenitor cells which reside in both the epithelial and stromal cell compartments of the basalis layer. Finding a definitive marker for endometrial epithelial progenitors (eEPCs) has proven difficult. A number of different markers have been suggested as putative progenitor markers including, N-cadherin, SSEA-1, AXIN2, SOX-9 and ALDH1A1, some of which show functional stem cell activity in assays. Each marker has a unique location(s) in the glandular epithelium, which has led to the suggestion that a differentiation hierarchy exists, from the base of epithelial glands in the basalis to the luminal epithelium lining the functionalis, where epithelial cells express different combinations of markers as they differentiate and move up the gland into the functionalis away from the basalis niche. Perivascular endometrial mesenchymal stem cells (eMSCs) can be identified by co-expression of PDGFRβ and CD146 or by a single marker, SUSD2. This review will detail the known endometrial stem/progenitor markers; their identity, location and known interactions and hierarchy across the menstrual cycle, in particular post-menstrual repair and estrogen-driven regeneration, as well as their possible contributions to menstruation-related disorders such as endometriosis and regeneration-related disorder Asherman's syndrome. We will also highlight new techniques that allow for a greater understanding of stem/progenitor cells' role in repair and regeneration, including 3D organoids, 3D slice cultures and gene sequencing at the single cell level. Since mouse models are commonly used to study menstruation, repair and regeneration we will also detail the mouse stem/progenitor markers that have been investigated .
人类子宫内膜是一种非凡的组织,在女性的生殖寿命期间经历约450个增殖、分化、脱落(月经)、修复和再生周期。月经后修复是一个极其快速且无疤痕的过程,在脱落开始后的48小时内,腔上皮的重新上皮化即可完成。月经结束后,在循环雌激素水平上升的影响下,功能层在增殖期从残留的基底层生长而来。子宫内膜的再生能力归因于位于基底层上皮和基质细胞区室中的干/祖细胞。事实证明,找到一种明确的子宫内膜上皮祖细胞(eEPC)标志物很困难。已经提出了许多不同的标志物作为假定的祖细胞标志物,包括N-钙黏蛋白、阶段特异性胚胎抗原-1(SSEA-1)、轴抑制蛋白2(AXIN2)、性别决定区Y盒9(SOX-9)和视黄醛脱氢酶1A1(ALDH1A1),其中一些在实验中显示出功能性干细胞活性。每个标志物在腺上皮中都有独特的定位,这表明存在一种分化层次结构,从基底层上皮腺体的底部到功能层内衬的腔上皮,在上皮细胞分化并从基底层龛向上移动到功能层的过程中,它们表达不同的标志物组合。血管周围的子宫内膜间充质干细胞(eMSC)可以通过血小板衍生生长因子受体β(PDGFRβ)和CD146的共表达或单一标志物SUSD2来识别。本综述将详细介绍已知的子宫内膜干/祖细胞标志物;它们的身份、位置以及在整个月经周期中已知的相互作用和层次结构,特别是月经后修复和雌激素驱动的再生,以及它们对诸如子宫内膜异位症等与月经相关的疾病和与再生相关的疾病阿谢曼综合征的可能影响。我们还将重点介绍有助于更深入了解干/祖细胞在修复和再生中作用的新技术,包括3D类器官、3D切片培养和单细胞水平的基因测序。由于小鼠模型通常用于研究月经、修复和再生,我们还将详细介绍已被研究的小鼠干/祖细胞标志物。