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Tendinopathy; encompassing multifactorial tendon disorders characterised by pain and functional limitation remains a significant burden in musculoskeletal medicine.1 Recent findings highlight a key role for immune mediated mechanisms in tendon disease supporting the concept that pivotal immunological and biomechanical factors conventionally associated with inflammatory rheumatic and musculoskeletal diseases (RMDs) are manifest in tendon.2 Single cell technologies3 (scRNAseq) are increasingly applied in rheumatology to identify key cellular phenotypes that drive disease pathogenesis. Despite efforts with small cell numbers and heterogenous tendon biopsies4 there remains no detailed spatial tendon cell atlas to inform translational targeting. Herein, for the first time utilising scRNAseq and spatial transcriptomics (ST), we carry out cell–cell interaction analysis to build an atlas of the dynamic cellular environment that drives the development of chronic human tendon disease.
In healthy (4 biopsies, n=3040 cells) and diseased (5 biopsies, n=19 084 cells) tendon we find a mix of endothelial, immune and stromal cells (figure 1A, online supplemental file 1). Each cell type group is present in disease and healthy tissue but with distinct quantitative and qualitative characteristics. Within stromal populations we identified ‘mural type’ stromal cells (figure 1B). Mural cells, which include pericytes, are possible progenitor cells in tendon5 and interestingly, these cells are phenotypically similar to NOTCH3 high mural cells described in rheumatoid arthritis (RA) synovium which can differentiate into fibroblasts following interactions with endothelial cells (ECs) via JAG1.6 Cell–cell interaction and ST analysis indicate a similar phenomenon could occur within tendinopathy between mural cells and SEMA3G ECs (figure 1F). In all diseased stromal cell populations, there was greater expression of genes for extracellular matrix proteins (eg, COL1A1, COL3A1, FN1, BGN) which is considered the hallmark feature of tendinopathy (online supplemental figure S2B). Furthermore, pathway analysis indicates stromal cell clusters shift from negative regulation of immune cell and cytokine responses in normal tendon (online supplemental figure S3A) to a state that promotes immune cell recruitment and activation along with cytokine secretion and response processes in diseased tendon (online supplemental figure S3B,C).
Seven subtypes of PECAM1+ ECs were found (figure 1D), including a population of LYVE1+ ECs that produce CCL21 and have been shown to regulate dendritic cell (DC) migration.7 Furthermore, CCL21 is upregulated in these cells in tendinopathy (online supplemental figure S2C). DCs comprise the single largest immune cell population present in normal tendon (figure 1B). Intriguingly, DCs are also present in diseased tendon however, showing therein greater levels of DC activation and lower levels of C1Q genes (regulatory DC markers) (online supplemental figure S2D,E). The activation of DCs and subsequent T cell activation8 in tendinopathy is further evidenced by pathway analysis of differentially upregulated genes in disease (online supplemental figure S3D,E). This activation may in part be due to increased matrix protein expression, such as FN1, which can activate DCs and resulting in alterations in T cell populations within tissue potentially contributing to mechanisms driving disease chronicity. Additionally, we found three populations of macrophages in diseased tendon, one of which, cycling macrophages (figure 1C, online supplemental figure S2A) is unique to diseased tissue. The transcript profile of macrophages in normal tendon most closely resembled tissue repair and debris clearance (figure 1E, online supplemental figure S2D). Within normal tendon we found APP expression in tenocytes which can induce a resolution promoting phenotype in macrophages. However, APP expression was reduced in the stromal compartment in disease coinciding with diminished expression of LYVE1 within diseased tissue macrophages (figure 1E, online supplemental figure S2D). These macrophage subsets have recently been associated with RA remission and we postulate the phenotypic drift away from this phenotype promotes aberrant tissue repair and attendant tendinopathy.9
Further evidence suggesting that the stromal environment may induce inflammatory changes comprises increased expression of MIF (figure 1E, online supplemental figure S2B) in diseased tenocytes that can induce proinflammatory effects via its receptor CD74, which is also upregulated in macrophages from diseased tendon (figure 1E, online supplemental figure S2C). ST generated indicative data from cell–cell interaction analysis suggests stromal induced immune regulation. As such, we postulate the primary role of the immune compartment within the tendon is to regulate and resolve damage; however, following cumulative microtrauma the fundamental process of debris removal and matrix repair initiated by tenocytes could lead to positive amplification of the immune compartment. We further propose that within diseased tendon immune homoeostasis may become imbalanced and activated immune cells, primed by both endothelial and stromal cells, promote a cycle of inflammation and aberrant tissue repair. The inflammatory environment, including cytokine pathways that are unequivocally demonstrated in this preliminary tendon atlas, have been targeted to yield potent immunological interventions in a range of inflammatory RMDs—the potential to target and investigate these pathways in human tendon disease is now compelling.
Patient consent for publication
All procedures and protocols were approved by the Ethics Committee under the approval number West of Scotland REC (REC14/WS/1035) with informed consent obtained and carried out in accordance with standard operative procedures.
We thank the CZI Tendon Seed Network for helpful discussions when preparing this manuscript for publication.
Handling editor Josef S Smolen
Contributors MA, LM and NM conceived and designed the experiments. MA, LM and KC performed experiments. IBM, NM, LANC, PS and SJBS provided expert advice. All authors analysed the data. MA, LANC, IBM and NM wrote the paper.
Funding This work was funded by the Medical Research Council (MR/R020515/1). SJBS was funded by the NIHR Oxford Biomedical Research Centre.
Competing interests KC and PS are scientific consultants to 10x Genomics.
Provenance and peer review Not commissioned; externally peer reviewed.
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