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Thy-1 plays a pathogenic role and is a potential biomarker for skin fibrosis in scleroderma
Roberta G. Marangoni, … , Christopher Ritchlin, Benjamin D. Korman
Roberta G. Marangoni, … , Christopher Ritchlin, Benjamin D. Korman
Published September 6, 2022
Citation Information: JCI Insight. 2022;7(19):e149426. https://doi.org/10.1172/jci.insight.149426.
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Research Article Dermatology Immunology

Thy-1 plays a pathogenic role and is a potential biomarker for skin fibrosis in scleroderma

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Abstract

Thy-1 (CD90) is a well-known marker of fibroblasts implicated in organ fibrosis, but its contribution to skin fibrosis remains unknown. We examined Thy-1 expression in scleroderma skin and its potential role as a biomarker and pathogenic factor in animal models of skin fibrosis. Skin from patients with systemic sclerosis demonstrated markedly elevated Thy-1 expression compared with controls, colocalized with fibroblast activator protein in the deep dermis, and correlated with the severity of skin involvement (modified Rodnan skin score). Serial imaging of skin from Thy-1 yellow fluorescent protein reporter mice by IVIS showed an increase in Thy-1 expression that correlated with onset and progression of fibrosis. In contrast to lung fibrosis, Thy-1–KO mice had attenuated skin fibrosis in both bleomycin and tight skin-1 murine models. Moreover, Thy-1 regulated key pathogenic pathways involved in fibrosis, including inflammation, myofibroblast differentiation, apoptosis, and multiple additional canonical fibrotic pathways. Therefore, although Thy-1 deficiency leads to exacerbated lung fibrosis, in skin it is protective. Moreover, Thy-1 may serve as a longitudinal marker to assess skin fibrosis.

Authors

Roberta G. Marangoni, Poulami Datta, Ananta Paine, Stacey Duemmel, Marc Nuzzo, Laura Sherwood, John Varga, Christopher Ritchlin, Benjamin D. Korman

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Figure 2

Thy-1 YFP can serve as an in vivo marker of skin fibrosis.

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Thy-1 YFP can serve as an in vivo marker of skin fibrosis.
(A) Represent...
(A) Representative images of YFP signal (radiance efficiency [photon/s/cm2/sr]/[μW/cm2]) measured at λ excitation max, 465 nm, and λ emission max, 520 nm by IVIS Spectrum after bleomycin injection. (B) Representative H&E-stained skin images showing temporal increase in dermal thickness induced by bleomycin. Scale bar: 100 μm. (C) Representative immunofluorescence imaging for Abs against pro–collagen type 1 (red, white arrowheads) as well as endogenous YFP label (green). Scale bar: 100 μm. (D) Average and (E) maximal YFP fluorescence radiance measured over time (days). Data are shown as mean ± SD. Tukey’s multiple-comparison test. *P < 0.05 compared with day 0. n = 3 per group. (F) Quantification of dermal thickness over time (days) in bleomycin-treated mice, as determined by 5 high-power fields per mouse. Values are the mean ± SD. P values calculated using 2-sided t test. *P ≤ 0.05 versus day 0. n = 3–4 per group. (G) Correlation between dermal thickness and YFP maximal fluorescence intensity by IVIS. Spearman’s rank correlation. (H) Number of procollagen-immunopositive cells per high-power field. Results are mean ± SD from 3 high-power fields per mouse. P values calculated using 2-sided t test. *P ≤ 0.05. n = 3. (I) Correlation between number of pro–collagen 1+ cells and YFP maximal fluorescence intensity. Spearman’s rank correlation test. (J) Gene expression changes over time (PAI1, ASMA, COL1A1, and THY1) in skin treated with bleomycin analyzed by qPCR. The thicker black line represents the mean of all fibrotic genes. Data represent mean gene expression per time point. n = 3–4. (K) Correlation between the average of fibrotic gene expression and YFP maximal fluorescence intensity. Spearman’s rank correlation test. PAI1, plasminogen activator inhibitor-1; ASMA, α–smooth muscle actin (ACTA2).

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