Persistent stromal fibroblast activation is present in chronic tendinopathy

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Persistent stromal fibroblast activation is present in chronic tendinopathy. / Dakin, Stephanie G.; Buckley, Christopher; Hussein Al-Mossawi, Mohammad; Hedley, Robert; O. Martinez, Fernando; Wheway, Kim; Watkins, Bridget; Carr, Andrew.

In: Arthritis Research & Therapy, Vol. 19, 16, 25.01.2017.

Research output: Contribution to journalArticlepeer-review

Harvard

Dakin, SG, Buckley, C, Hussein Al-Mossawi, M, Hedley, R, O. Martinez, F, Wheway, K, Watkins, B & Carr, A 2017, 'Persistent stromal fibroblast activation is present in chronic tendinopathy', Arthritis Research & Therapy, vol. 19, 16. https://doi.org/10.1186/s13075-016-1218-4

APA

Dakin, S. G., Buckley, C., Hussein Al-Mossawi, M., Hedley, R., O. Martinez, F., Wheway, K., Watkins, B., & Carr, A. (2017). Persistent stromal fibroblast activation is present in chronic tendinopathy. Arthritis Research & Therapy, 19, [16]. https://doi.org/10.1186/s13075-016-1218-4

Vancouver

Author

Dakin, Stephanie G. ; Buckley, Christopher ; Hussein Al-Mossawi, Mohammad ; Hedley, Robert ; O. Martinez, Fernando ; Wheway, Kim ; Watkins, Bridget ; Carr, Andrew. / Persistent stromal fibroblast activation is present in chronic tendinopathy. In: Arthritis Research & Therapy. 2017 ; Vol. 19.

Bibtex

@article{65b78ec39abf4627b30b91e967520cb3,
title = "Persistent stromal fibroblast activation is present in chronic tendinopathy",
abstract = "BackgroundGrowing evidence supports a key role for inflammation in the onset and progression of tendinopathy. However, the effect of the inflammatory infiltrate on tendon cells is poorly understood.MethodsWe investigated stromal fibroblast activation signatures in tissues and cells from patients with tendinopathy. Diseased tendons were collected from well-phenotyped patient cohorts with supraspinatus tendinopathy before and after sub-acromial decompression treatment. Healthy tendons were collected from patients undergoing shoulder stabilisation or anterior cruciate ligament repair. Stromal fibroblast activation markers including podoplanin (PDPN), CD106 (VCAM-1) and CD248 were investigated by immunostaining, flow cytometry and RT-qPCR.ResultsPDPN, CD248 and CD106 were increased in diseased compared to healthy tendon tissues. This stromal fibroblast activation signature persisted in tendon biopsies in patients at 2–4 years post treatment. PDPN, CD248 and CD106 were increased in diseased compared to healthy tendon cells. IL-1β treatment induced PDPN and CD106 but not CD248. IL-1β treatment induced NF-κB target genes in healthy cells, which gradually declined following replacement with cytokine-free medium, whilst PDPN and CD106 remained above pre-stimulated levels. IL-1β-treated diseased cells had more profound induction of PDPN and CD106 and sustained expression of IL6 and IL8 mRNA compared to IL-1β-treated healthy cells.ConclusionsWe conclude that stromal fibroblast activation markers are increased and persist in diseased compared to healthy tendon tissues and cells. Diseased tendon cells have distinct stromal fibroblast populations. IL-1β treatment induced persistent stromal fibroblast activation which was more profound in diseased cells. Persistent stromal fibroblast activation may be implicated in the development of chronic inflammation and recurrent tendinopathy. Targeting this stromal fibroblast activation signature is a potential therapeutic strategy.",
keywords = "Tendon, Tendinopathy, Inflammation, Stromal fibroblast",
author = "Dakin, {Stephanie G.} and Christopher Buckley and {Hussein Al-Mossawi}, Mohammad and Robert Hedley and {O. Martinez}, Fernando and Kim Wheway and Bridget Watkins and Andrew Carr",
year = "2017",
month = jan,
day = "25",
doi = "10.1186/s13075-016-1218-4",
language = "English",
volume = "19",
journal = "Arthritis Research & Therapy",
issn = "1478-6354",
publisher = "Springer",

}

RIS

TY - JOUR

T1 - Persistent stromal fibroblast activation is present in chronic tendinopathy

AU - Dakin, Stephanie G.

AU - Buckley, Christopher

AU - Hussein Al-Mossawi, Mohammad

AU - Hedley, Robert

AU - O. Martinez, Fernando

AU - Wheway, Kim

AU - Watkins, Bridget

AU - Carr, Andrew

PY - 2017/1/25

Y1 - 2017/1/25

N2 - BackgroundGrowing evidence supports a key role for inflammation in the onset and progression of tendinopathy. However, the effect of the inflammatory infiltrate on tendon cells is poorly understood.MethodsWe investigated stromal fibroblast activation signatures in tissues and cells from patients with tendinopathy. Diseased tendons were collected from well-phenotyped patient cohorts with supraspinatus tendinopathy before and after sub-acromial decompression treatment. Healthy tendons were collected from patients undergoing shoulder stabilisation or anterior cruciate ligament repair. Stromal fibroblast activation markers including podoplanin (PDPN), CD106 (VCAM-1) and CD248 were investigated by immunostaining, flow cytometry and RT-qPCR.ResultsPDPN, CD248 and CD106 were increased in diseased compared to healthy tendon tissues. This stromal fibroblast activation signature persisted in tendon biopsies in patients at 2–4 years post treatment. PDPN, CD248 and CD106 were increased in diseased compared to healthy tendon cells. IL-1β treatment induced PDPN and CD106 but not CD248. IL-1β treatment induced NF-κB target genes in healthy cells, which gradually declined following replacement with cytokine-free medium, whilst PDPN and CD106 remained above pre-stimulated levels. IL-1β-treated diseased cells had more profound induction of PDPN and CD106 and sustained expression of IL6 and IL8 mRNA compared to IL-1β-treated healthy cells.ConclusionsWe conclude that stromal fibroblast activation markers are increased and persist in diseased compared to healthy tendon tissues and cells. Diseased tendon cells have distinct stromal fibroblast populations. IL-1β treatment induced persistent stromal fibroblast activation which was more profound in diseased cells. Persistent stromal fibroblast activation may be implicated in the development of chronic inflammation and recurrent tendinopathy. Targeting this stromal fibroblast activation signature is a potential therapeutic strategy.

AB - BackgroundGrowing evidence supports a key role for inflammation in the onset and progression of tendinopathy. However, the effect of the inflammatory infiltrate on tendon cells is poorly understood.MethodsWe investigated stromal fibroblast activation signatures in tissues and cells from patients with tendinopathy. Diseased tendons were collected from well-phenotyped patient cohorts with supraspinatus tendinopathy before and after sub-acromial decompression treatment. Healthy tendons were collected from patients undergoing shoulder stabilisation or anterior cruciate ligament repair. Stromal fibroblast activation markers including podoplanin (PDPN), CD106 (VCAM-1) and CD248 were investigated by immunostaining, flow cytometry and RT-qPCR.ResultsPDPN, CD248 and CD106 were increased in diseased compared to healthy tendon tissues. This stromal fibroblast activation signature persisted in tendon biopsies in patients at 2–4 years post treatment. PDPN, CD248 and CD106 were increased in diseased compared to healthy tendon cells. IL-1β treatment induced PDPN and CD106 but not CD248. IL-1β treatment induced NF-κB target genes in healthy cells, which gradually declined following replacement with cytokine-free medium, whilst PDPN and CD106 remained above pre-stimulated levels. IL-1β-treated diseased cells had more profound induction of PDPN and CD106 and sustained expression of IL6 and IL8 mRNA compared to IL-1β-treated healthy cells.ConclusionsWe conclude that stromal fibroblast activation markers are increased and persist in diseased compared to healthy tendon tissues and cells. Diseased tendon cells have distinct stromal fibroblast populations. IL-1β treatment induced persistent stromal fibroblast activation which was more profound in diseased cells. Persistent stromal fibroblast activation may be implicated in the development of chronic inflammation and recurrent tendinopathy. Targeting this stromal fibroblast activation signature is a potential therapeutic strategy.

KW - Tendon

KW - Tendinopathy

KW - Inflammation

KW - Stromal fibroblast

U2 - 10.1186/s13075-016-1218-4

DO - 10.1186/s13075-016-1218-4

M3 - Article

VL - 19

JO - Arthritis Research & Therapy

JF - Arthritis Research & Therapy

SN - 1478-6354

M1 - 16

ER -