Mast cells are a source of transforming growth factor β in systemic sclerosis

Objective To describe the cellular source of transforming growth factor β (TGFβ) in the dermis of patients with systemic sclerosis (SSc). Methods We performed electron microscopy (EM) with immunogold labeling on skin biopsy specimens from 7 patients with SSc and 3 healthy control subjects. For TGFβ...

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Published inArthritis and rheumatism Vol. 63; no. 3; pp. 795 - 799
Main Authors Hügle, Thomas, Hogan, Vanessa, White, Kathryn E., van Laar, Jacob M.
Format Journal Article
LanguageEnglish
Published Hoboken Wiley Subscription Services, Inc., A Wiley Company 01.03.2011
Wiley
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ISSN0004-3591
1529-0131
1529-0131
DOI10.1002/art.30190

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Summary:Objective To describe the cellular source of transforming growth factor β (TGFβ) in the dermis of patients with systemic sclerosis (SSc). Methods We performed electron microscopy (EM) with immunogold labeling on skin biopsy specimens from 7 patients with SSc and 3 healthy control subjects. For TGFβ quantification, the numbers of gold particles per square micron were calculated. The origin of mast cells was confirmed and quantified by toluidine blue staining and light microscopy. Degranulation was assessed on toluidine blue–stained sections and on EM images. Results In all patients, active TGFβ was observed uniquely in mast cell vesicles, some of which were released into the extracellular space. Patients with progressive SSc and a more recent onset of non–Raynaud's phenomenon symptoms had higher numbers of mast cells and gold particles per mast cell. Mast cells from healthy control subjects also contained active TGFβ but, in contrast to SSc samples, showed a resting character with no or low‐level degranulation and uniformly dense osmiophilic vesicles. Conclusion Degranulation of skin mast cells can be an important mechanism of TGFβ secretion in SSc.
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ISSN:0004-3591
1529-0131
1529-0131
DOI:10.1002/art.30190