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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共 52 条
  • [1] Low pericyte coverage of endometrial microvessels in heavy menstrual bleeding correlates with the microvessel expression of VEGF-A
    Andersson, Emil
    Zetterberg, Eva
    Vedin, Inger
    Hultenby, Kjell
    Palmblad, Jan
    Mints, Miriam
    [J]. INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE, 2015, 35 (02) : 433 - 438
  • [2] Pericytes in wound healing: friend or foe?
    Ansell, David M.
    Izeta, Ander
    [J]. EXPERIMENTAL DERMATOLOGY, 2015, 24 (11) : 833 - 834
  • [3] Characterization of human-like menstruation in the spiny mouse: comparative studies with the human and induced mouse model
    Bellofiore, Nadia
    Rana, Shreya
    Dickinson, Hayley
    Temple-Smith, Peter
    Evans, Jemma
    [J]. HUMAN REPRODUCTION, 2018, 33 (09) : 1715 - 1726
  • [4] A missing piece: the spiny mouse and the puzzle of menstruating species
    Bellofiore, Nadia
    Cousins, Fiona
    Temple-Smith, Peter
    Dickinson, Hayley
    Evans, Jemma
    [J]. JOURNAL OF MOLECULAR ENDOCRINOLOGY, 2018, 61 (01) : R25 - R41
  • [5] Pericytes: A newly recognized player in wound healing
    Bodnar, Richard J.
    Satish, Latha
    Yates, Cecelia C.
    Wells, Alan
    [J]. WOUND REPAIR AND REGENERATION, 2016, 24 (02) : 204 - 214
  • [6] Caligioni C.S., 2009, CURR PROTOC NEUROSCI, V48, pA, DOI [10.1002/0471142301.nsa04is48, DOI 10.1002/0471142301.NSA04IS48]
  • [7] Identification, characterization and co-localization of label-retaining cell population in mouse endometrium with typical undifferentiated markers
    Cervello, I.
    Martinez-Conejero, J. A.
    Horcajadas, J. A.
    Pellicer, A.
    Simon, C.
    [J]. HUMAN REPRODUCTION, 2007, 22 (01) : 45 - 51
  • [8] Identification of label-retaining cells in mouse endometrium
    Chan, Rachel W. S.
    Gargett, Caroline E.
    [J]. STEM CELLS, 2006, 24 (06) : 1529 - 1538
  • [9] Clonogenicity of human endometrial epithelial and stromal cellss
    Chan, RWS
    Schwab, KE
    Gargett, CE
    [J]. BIOLOGY OF REPRODUCTION, 2004, 70 (06) : 1738 - 1750
  • [10] Characteristics of Human Endometrium-Derived Mesenchymal Stem Cells and Their Tropism to Endometriosis
    Cheng, Yan
    Li, Liru
    Wang, Dejun
    Guo, Qiuyan
    He, Yanan
    Liang, Tian
    Sun, Liyuan
    Wang, Xiaojun
    Cheng, Yulei
    Zhang, Guangmei
    [J]. STEM CELLS INTERNATIONAL, 2017, 2017