Single-cell RNA sequencing redefines the mesenchymal cell landscape of mouse endometrium
Autor: | Philippa T. K. Saunders, Olympia Kelepouri, James R Smith, Arantza Esnal-Zufiaurre, Douglas A Gibson, Neil C. Henderson, Ross Dobie, John R. Wilson-Kanamori, Phoebe M. Kirkwood |
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Rok vydání: | 2020 |
Předmět: |
0301 basic medicine
Stromal cell Mesenchyme Green Fluorescent Proteins CD34 Biology Biochemistry Receptor Platelet-Derived Growth Factor beta 03 medical and health sciences Endometrium Mice 0302 clinical medicine Genetics medicine Animals Homeostasis Progenitor cell CXCL14 Molecular Biology Sequence Analysis RNA Mesenchymal stem cell Mesenchymal Stem Cells Cell biology 030104 developmental biology medicine.anatomical_structure Gene Expression Regulation CD146 Female Pericyte Single-Cell Analysis Transcriptome 030217 neurology & neurosurgery Biomarkers Biotechnology |
Zdroj: | Kirkwood, P M, Gibson, D A, Smith, J R, Wilson-Kanamori, J R, Kelepouri, O, Esnal-Zufiaurre, A, Dobie, R, Henderson, N C & Saunders, P T K 2021, ' Single-cell RNA sequencing redefines the mesenchymal cell landscape of mouse endometrium ', The FASEB Journal, vol. 35, no. 4, e21285 . https://doi.org/10.1096/fj.202002123R |
ISSN: | 1530-6860 |
DOI: | 10.1096/fj.202002123R |
Popis: | 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 PDGFRβ + 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 PDGFRα+/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. |
Databáze: | OpenAIRE |
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