Taxonomy of fibroblasts and progenitors in the synovial joint at single-cell resolution

被引:27
作者
Collins, Fraser L. [1 ]
Roelofs, Anke J. [1 ]
Symons, Rebecca A. [1 ]
Kania, Karolina [1 ]
Campbell, Ewan [2 ]
Collie-duguid, Elaina S. R. [2 ]
Riemen, Anna H. K. [1 ]
Clark, Susan M. [1 ]
De Bari, Cosimo [1 ]
机构
[1] Univ Aberdeen, Ctr Arthrit & Musculoskeletal Hlth, Arthrit & Regenerat Med Lab, Aberdeen, Scotland
[2] Univ Aberdeen, Ctr Genome Enabled Biol & Med, Aberdeen, Scotland
基金
英国医学研究理事会;
关键词
Fibroblasts; Synovitis; Osteoarthritis; Knee; ARTICULAR-CARTILAGE FORMATION; SUPERFICIAL ZONE; IDENTIFICATION; REGULATORS; EXPRESSION; LINEAGES;
D O I
10.1136/ard-2021-221682
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
ObjectivesFibroblasts 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. MethodsTo discriminate between Gdf5-lineage cells deriving from the embryonic joint interzone and other Pdgfr alpha-expressing fibroblasts and progenitors, adult Gdf5-Cre;Tom;Pdgfr alpha-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. ResultsIn 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. ConclusionsOur 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.
引用
收藏
页码:428 / 437
页数:10
相关论文
共 38 条
[1]   Generalizing RNA velocity to transient cell states through dynamical modeling [J].
Bergen, Volker ;
Lange, Marius ;
Peidli, Stefan ;
Wolf, F. Alexander ;
Theis, Fabian J. .
NATURE BIOTECHNOLOGY, 2020, 38 (12) :1408-1414
[2]   Cross-tissue organization of the fibroblast lineage [J].
Buechler, Matthew B. ;
Pradhan, Rachana N. ;
Krishnamurty, Akshay T. ;
Cox, Christian ;
Calviello, Aslihan Karabacak ;
Wang, Amber W. ;
Yang, Yeqing Angela ;
Tam, Lucinda ;
Caothien, Roger ;
Roose-Girma, Merone ;
Modrusan, Zora ;
Arron, Joseph R. ;
Bourgon, Richard ;
Muller, Soren ;
Turley, Shannon. J. .
NATURE, 2021, 593 (7860) :575-+
[3]   Heads, Shoulders, Elbows, Knees, and Toes: Modular Gdf5 Enhancers Control Different Joints in the Vertebrate Skeleton [J].
Chen, Hao ;
Capellini, Terence D. ;
Schoor, Michael ;
Mortlock, Doug P. ;
Reddi, A. Hari ;
Kingsley, David M. .
PLOS GENETICS, 2016, 12 (11)
[4]   Synovial cell cross-talk with cartilage plays a major role in the pathogenesis of osteoarthritis [J].
Chou, Ching-Heng ;
Jain, Vaibhav ;
Gibson, Jason ;
Attarian, David E. ;
Haraden, Collin A. ;
Yohn, Christopher B. ;
Laberge, Remi-Martin ;
Gregory, Simon ;
Kraus, Virginia B. .
SCIENTIFIC REPORTS, 2020, 10 (01)
[5]   Inflammation and Its Role in Regeneration and Repair A Caution for Novel Anti-Inflammatory Therapies [J].
Cooke, John P. .
CIRCULATION RESEARCH, 2019, 124 (08) :1166-1168
[6]   Distinct fibroblast subsets drive inflammation and damage in arthritis [J].
Croft, Adam P. ;
Campos, Joana ;
Jansen, Kathrin ;
Turner, Jason D. ;
Marshall, Jennifer ;
Attar, Moustafa ;
Savary, Loriane ;
Wehmeyer, Corinna ;
Naylor, Amy J. ;
Kemble, Samuel ;
Begum, Jenefa ;
Durholz, Kerstin ;
Perlman, Harris ;
Barone, Francesca ;
McGettrick, Helen M. ;
Fearon, Douglas T. ;
Wei, Kevin ;
Raychaudhuri, Soumya ;
Korsunsky, Ilya ;
Brenner, Michael B. ;
Coles, Mark ;
Sansom, Stephen N. ;
Filer, Andrew ;
Buckley, Christopher D. .
NATURE, 2019, 570 (7760) :246-+
[7]   Cell origin, volume and arrangement are drivers of articular cartilage formation, morphogenesis and response to injury in mouse limbs [J].
Decker, Rebekah S. ;
Um, Hyo-Bin ;
Dyment, Nathaniel A. ;
Cottingham, Naiga ;
Usami, Yu ;
Enomoto-Iwamoto, Motomi ;
Kronenberg, Mark S. ;
Maye, Peter ;
Rowe, David W. ;
Koyama, Eiki ;
Pacifici, Maurizio .
DEVELOPMENTAL BIOLOGY, 2017, 426 (01) :56-68
[8]   Distinct fibroblast lineages determine dermal architecture in skin development and repair [J].
Driskell, Ryan R. ;
Lichtenberger, Beate M. ;
Hoste, Esther ;
Kretzschmar, Kai ;
Simons, Ben D. ;
Charalambous, Marika ;
Ferron, Sacri R. ;
Herault, Yann ;
Pavlovic, Guillaume ;
Ferguson-Smith, Anne C. ;
Watt, Fiona M. .
NATURE, 2013, 504 (7479) :277-+
[9]   Regulation of Gdf5 expression in joint remodelling, repair and osteoarthritis [J].
Kania, Karolina ;
Colella, Fabio ;
Riemen, Anna H. K. ;
Wang, Hui ;
Howard, Kenneth A. ;
Aigner, Thomas ;
Dell'Accio, Francesco ;
Capellini, Terence D. ;
Roelofs, Anke J. ;
De Bari, Cosimo .
SCIENTIFIC REPORTS, 2020, 10 (01)
[10]  
Khan IM, 2001, ARTHRITIS RHEUM, V44, P1795, DOI 10.1002/1529-0131(200108)44:8<1795::AID-ART316>3.0.CO