Center for Reproductive Biology; Department of Animal Sciences; Washington State University; Pullman, WA USA.
Cell Cycle. 2013 Sep 1;12(17):2888-98. doi: 10.4161/cc.25917.
The uterus is an extremely plastic organ that undergoes cyclical remodeling including endometrial regeneration during the menstrual cycle. Endometrial remodeling and regeneration also occur during pregnancy and following parturition, particularly in hemochorial implanting species. The mechanisms of endometrial regeneration are not well understood. Endometrial stem/progenitor cells are proposed to contribute to endometrial regeneration in both humans and mice. BrdU label retention has been used to identify potential stem/progenitor cells in mouse endometrium. However, methods are not available to isolate BrdU label-retaining cells (LRC) for functional analyses. Therefore, we employed a transgenic mouse model to identify H2B-GFP LRCs throughout the female reproductive tract with particular interest on the endometrium. We hypothesized that the female reproductive tract contains a population of long-term LRCs that persist even following pregnancy and endometrial regeneration. Endometrial cells were labeled (pulsed) either transplacentally/translactationally or peripubertally. When mice were pulsed transplacentally/translactationally, the label was not retained in the uterus. However, LRCs were concentrated to the distal oviduct and endocervical transition zone (TZ) following natural (i.e., pregnancy/parturition induced) and mechanically induced endometrial regeneration. LRCs in the distal oviduct and endocervical TZ expressed stem cell markers and did not express ERα or PGR, implying the undifferentiated phenotype of these cells. Oviduct and endocervical TZ LRCs did not proliferate during endometrial re-epithelialization, suggesting that they do not contribute to the endometrium in a stem/progenitor cell capacity. In contrast, when mice were pulsed peripubertally long-term LRCs were identified in the endometrial glandular compartment in mice as far out as 9 months post-pulse. These findings suggest that epithelial tissue of the female reproductive tract contains 3 distinct populations of epithelial cells that exhibit stem/progenitor cell qualities. Distinct stem/progenitor-like cells localize to the oviduct, endometrium, and cervix.
子宫是一个极具可塑性的器官,在月经周期中经历周期性重塑,包括子宫内膜再生。子宫内膜重塑和再生也发生在怀孕期间和分娩后,特别是在血绒毛膜植入物种中。子宫内膜再生的机制尚不清楚。子宫内膜干细胞/祖细胞被认为有助于人和小鼠的子宫内膜再生。BrdU 标记保留已被用于鉴定小鼠子宫内膜中的潜在干细胞/祖细胞。然而,目前尚无方法可分离 BrdU 标记保留细胞(LRC)进行功能分析。因此,我们采用了一种转基因小鼠模型来鉴定整个雌性生殖道中的 H2B-GFP LRC,特别关注子宫内膜。我们假设,雌性生殖道中存在一群长期的 LRC,即使在怀孕和子宫内膜再生后也能持续存在。子宫内膜细胞要么经胎盘/乳腺途径,要么经青春期前被标记(脉冲)。当小鼠经胎盘/乳腺途径被脉冲标记时,标记不会保留在子宫中。然而,LRC 集中在远端输卵管和宫颈内口过渡区(TZ),无论是在自然(即怀孕/分娩诱导)和机械诱导的子宫内膜再生后。远端输卵管和宫颈内口 TZ 的 LRC 表达干细胞标志物,不表达 ERα 或 PGR,这意味着这些细胞的未分化表型。输卵管和宫颈内口 TZ 的 LRC 在子宫内膜再上皮化过程中不增殖,表明它们不以干细胞/祖细胞的能力为子宫内膜做出贡献。相比之下,当小鼠在青春期前被脉冲标记时,在远至脉冲后 9 个月的小鼠子宫内膜腺腔中也可以识别到长期 LRC。这些发现表明,雌性生殖道的上皮组织包含 3 种具有干细胞/祖细胞特性的上皮细胞群体。不同的类干细胞样细胞定位于输卵管、子宫内膜和宫颈。