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Taxonomy of fibroblasts and progenitors in the synovial joint at single-cell resolution
OBJECTIVES: Fibroblasts in synovium include fibroblast-like synoviocytes (FLS) in the lining and Thy1+ connective-tissue fibroblasts in the sublining. We aimed to investigate their developmental origin and relationship with adult progenitors. METHODS: To discriminate between Gdf5-lineage cells deriv...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BMJ Publishing Group
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9933170/ https://www.ncbi.nlm.nih.gov/pubmed/36414376 http://dx.doi.org/10.1136/ard-2021-221682 |
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author | Collins, Fraser L Roelofs, Anke J Symons, Rebecca A Kania, Karolina Campbell, Ewan Collie-duguid, Elaina S R Riemen, Anna H K Clark, Susan M De Bari, Cosimo |
author_facet | Collins, Fraser L Roelofs, Anke J Symons, Rebecca A Kania, Karolina Campbell, Ewan Collie-duguid, Elaina S R Riemen, Anna H K Clark, Susan M De Bari, Cosimo |
author_sort | Collins, Fraser L |
collection | PubMed |
description | OBJECTIVES: Fibroblasts in synovium include fibroblast-like synoviocytes (FLS) in the lining and Thy1+ connective-tissue fibroblasts in the sublining. We aimed to investigate their developmental origin and relationship with adult progenitors. METHODS: To discriminate between Gdf5-lineage cells deriving from the embryonic joint interzone and other Pdgfrα-expressing fibroblasts and progenitors, adult Gdf5-Cre;Tom;Pdgfrα-H2BGFP mice were used and cartilage injury was induced to activate progenitors. Cells were isolated from knees, fibroblasts and progenitors were sorted by fluorescence-activated cell-sorting based on developmental origin, and analysed by single-cell RNA-sequencing. Flow cytometry and immunohistochemistry were used for validation. Clonal-lineage mapping was performed using Gdf5-Cre;Confetti mice. RESULTS: In steady state, Thy1+ sublining fibroblasts were of mixed ontogeny. In contrast, Thy1-Prg4+ lining fibroblasts predominantly derived from the embryonic joint interzone and included Prg4-expressing progenitors distinct from molecularly defined FLS. Clonal-lineage tracing revealed compartmentalisation of Gdf5-lineage fibroblasts between lining and sublining. Following injury, lining hyperplasia resulted from proliferation and differentiation of Prg4-expressing progenitors, with additional recruitment of non-Gdf5-lineage cells, into FLS. Consistent with this, a second population of proliferating cells, enriched near blood vessels in the sublining, supplied activated multipotent cells predicted to give rise to Thy1+ fibroblasts, and to feed into the FLS differentiation trajectory. Transcriptional programmes regulating fibroblast differentiation trajectories were uncovered, identifying Sox5 and Foxo1 as key FLS transcription factors in mice and humans. CONCLUSIONS: Our findings blueprint a cell atlas of mouse synovial fibroblasts and progenitors in healthy and injured knees, and provide novel insights into the cellular and molecular principles governing the organisation and maintenance of adult synovial joints. |
format | Online Article Text |
id | pubmed-9933170 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BMJ Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-99331702023-02-17 Taxonomy of fibroblasts and progenitors in the synovial joint at single-cell resolution Collins, Fraser L Roelofs, Anke J Symons, Rebecca A Kania, Karolina Campbell, Ewan Collie-duguid, Elaina S R Riemen, Anna H K Clark, Susan M De Bari, Cosimo Ann Rheum Dis Animal Models OBJECTIVES: Fibroblasts in synovium include fibroblast-like synoviocytes (FLS) in the lining and Thy1+ connective-tissue fibroblasts in the sublining. We aimed to investigate their developmental origin and relationship with adult progenitors. METHODS: To discriminate between Gdf5-lineage cells deriving from the embryonic joint interzone and other Pdgfrα-expressing fibroblasts and progenitors, adult Gdf5-Cre;Tom;Pdgfrα-H2BGFP mice were used and cartilage injury was induced to activate progenitors. Cells were isolated from knees, fibroblasts and progenitors were sorted by fluorescence-activated cell-sorting based on developmental origin, and analysed by single-cell RNA-sequencing. Flow cytometry and immunohistochemistry were used for validation. Clonal-lineage mapping was performed using Gdf5-Cre;Confetti mice. RESULTS: In steady state, Thy1+ sublining fibroblasts were of mixed ontogeny. In contrast, Thy1-Prg4+ lining fibroblasts predominantly derived from the embryonic joint interzone and included Prg4-expressing progenitors distinct from molecularly defined FLS. Clonal-lineage tracing revealed compartmentalisation of Gdf5-lineage fibroblasts between lining and sublining. Following injury, lining hyperplasia resulted from proliferation and differentiation of Prg4-expressing progenitors, with additional recruitment of non-Gdf5-lineage cells, into FLS. Consistent with this, a second population of proliferating cells, enriched near blood vessels in the sublining, supplied activated multipotent cells predicted to give rise to Thy1+ fibroblasts, and to feed into the FLS differentiation trajectory. Transcriptional programmes regulating fibroblast differentiation trajectories were uncovered, identifying Sox5 and Foxo1 as key FLS transcription factors in mice and humans. CONCLUSIONS: Our findings blueprint a cell atlas of mouse synovial fibroblasts and progenitors in healthy and injured knees, and provide novel insights into the cellular and molecular principles governing the organisation and maintenance of adult synovial joints. BMJ Publishing Group 2023-03 2022-11-22 /pmc/articles/PMC9933170/ /pubmed/36414376 http://dx.doi.org/10.1136/ard-2021-221682 Text en © Author(s) (or their employer(s)) 2023. Re-use permitted under CC BY. Published by BMJ. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution 4.0 Unported (CC BY 4.0) license, which permits others to copy, redistribute, remix, transform and build upon this work for any purpose, provided the original work is properly cited, a link to the licence is given, and indication of whether changes were made. See: https://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Animal Models Collins, Fraser L Roelofs, Anke J Symons, Rebecca A Kania, Karolina Campbell, Ewan Collie-duguid, Elaina S R Riemen, Anna H K Clark, Susan M De Bari, Cosimo Taxonomy of fibroblasts and progenitors in the synovial joint at single-cell resolution |
title | Taxonomy of fibroblasts and progenitors in the synovial joint at single-cell resolution |
title_full | Taxonomy of fibroblasts and progenitors in the synovial joint at single-cell resolution |
title_fullStr | Taxonomy of fibroblasts and progenitors in the synovial joint at single-cell resolution |
title_full_unstemmed | Taxonomy of fibroblasts and progenitors in the synovial joint at single-cell resolution |
title_short | Taxonomy of fibroblasts and progenitors in the synovial joint at single-cell resolution |
title_sort | taxonomy of fibroblasts and progenitors in the synovial joint at single-cell resolution |
topic | Animal Models |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9933170/ https://www.ncbi.nlm.nih.gov/pubmed/36414376 http://dx.doi.org/10.1136/ard-2021-221682 |
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