Single-cell RNA sequencing redefines the mesenchymal cell landscape of mouse endometrium

被引:51
作者
Kirkwood, Phoebe M. [1 ]
Gibson, Douglas A. [1 ]
Smith, James R. [1 ]
Wilson-Kanamori, John R. [1 ]
Kelepouri, Olympia [1 ]
Esnal-Zufiaurre, Arantza [1 ]
Dobie, Ross [1 ]
Henderson, Neil C. [1 ,2 ]
Saunders, Philippa T. K. [1 ]
机构
[1] Univ Edinburgh, Ctr Inflammat Res, 47 Little France Crescent, Edinburgh EH16 4TJ, Midlothian, Scotland
[2] Univ Edinburgh, Inst Genet & Mol Med, MRC Human Genet Unit, Edinburgh, Midlothian, Scotland
基金
英国惠康基金; 英国医学研究理事会;
关键词
CD146; chondroitin sulfate proteoglycan 4; endometrium; fibroblast; pericyte; platelet‐ derived growth factor beta; STEM-CELLS; PERIVASCULAR CELLS; STROMAL CELLS; KIDNEY INJURY; R PACKAGE; EXPRESSION; IDENTIFICATION; DECIDUALIZATION; PERICYTES; MARKERS;
D O I
10.1096/fj.202002123R
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The endometrium is a dynamic tissue that exhibits remarkable resilience to repeated episodes of differentiation, breakdown, regeneration, and remodeling. Endometrial physiology relies on a complex interplay between the stromal and epithelial compartments with the former containing a mixture of fibroblasts, vascular, and immune cells. There is evidence for rare populations of putative mesenchymal progenitor cells located in the perivascular niche of human endometrium, but the existence of an equivalent cell population in mouse is unclear. We used the Pdgfrb-BAC-eGFP transgenic reporter mouse in combination with bulk and single-cell RNA sequencing to redefine the endometrial mesenchyme. In contrast to previous reports we show that CD146 is expressed in both PDGFR beta + perivascular cells and CD31 + endothelial cells. Bulk RNAseq revealed cells in the perivascular niche which express the high levels of Pdgfrb as well as genes previously identified in pericytes and/or vascular smooth muscle cells (Acta2, Myh11, Olfr78, Cspg4, Rgs4, Rgs5, Kcnj8, and Abcc9). scRNA-seq identified five subpopulations of cells including closely related pericytes/vascular smooth muscle cells and three subpopulations of fibroblasts. All three fibroblast populations were PDGFR alpha+/CD34 + but were distinct in their expression of Ngfr/Spon2/Angptl7 (F1), Cxcl14/Smoc2/Rgs2 (F2), and Clec3b/Col14a1/Mmp3 (F3), with potential functions in the regulation of immune responses, response to wounding, and organization of extracellular matrix, respectively. Immunohistochemistry was used to investigate the spatial distribution of these populations revealing F1/NGFR + cells in most abundance beside epithelial cells. We provide the first definitive analysis of mesenchymal cells in the adult mouse endometrium identifying five subpopulations providing a platform for comparisons between mesenchymal cells in endometrium and other adult tissues which are prone to fibrosis.
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页数:21
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