S100A4 amplifies TGF-β-induced fibroblast activation in systemic sclerosis

Michal Tomcik; Katrin Palumbo-Zerr; Pawel Zerr; Jerome Avouac; Clara Dees; Barbora Sumova; Alfiya Distler; Christian Beyer; Lucie Andres Cerezo; Radim Becvar; Oliver Distler; Mariam Grigorian; Georg Schett; Ladislav Senolt; Jörg H W Distler

doi:10.1136/annrheumdis-2013-204516

S100A4 amplifies TGF-β-induced fibroblast activation in systemic sclerosis

Michal Tomcik, Katrin Palumbo-Zerr, Pawel Zerr, Jerome Avouac, Clara Dees, Barbora Sumova, Alfiya Distler, Christian Beyer, Lucie Andres Cerezo, Radim Becvar, Oliver Distler, Mariam Grigorian, Georg Schett, Ladislav Senolt, Jörg H W Distler

32 Citations (Scopus)

Abstract

OBJECTIVES: S100A4 is a calcium binding protein with regulatory functions in cell homeostasis, proliferation and differentiation that has been shown to promote cancer progression and metastasis. In the present study, we evaluated the role of S100A4 in fibroblast activation in systemic sclerosis (SSc).

METHODS: The expression of S100A4 was analysed in human samples, murine models of SSc and in cultured fibroblasts by real-time PCR, immunohistochemistry and western blot. The functional role of S100A4 was evaluated using siRNA, overexpression, recombinant protein and S100A4 knockout (S100A4(-/-)) mice. Transforming growth factor β (TGF-β) signalling was assessed by reporter assays, staining for phosphorylated Smad2/3 and analyses of target genes.

RESULTS: The expression of S100A4 was increased in SSc skin and in experimental fibrosis in a TGF-β/Smad-dependent manner. Overexpression of S100A4 or stimulation with recombinant S100A4 induced an activated phenotype in resting normal fibroblasts. In contrast, knockdown of S100A4 reduced the pro-fibrotic effects of TGF-β and decreased the release of collagen. S100A4(-/-) mice were protected from bleomycin-induced skin fibrosis with reduced dermal thickening, decreased hydroxyproline content and lower myofibroblast counts. Deficiency of S100A4 also ameliorated fibrosis in the tight-skin-1 (Tsk-1) mouse model.

CONCLUSIONS: We characterised S100A4 as a downstream mediator of the stimulatory effects of TGF-β on fibroblasts in SSc. TGF-β induces the expression of S100A4 to stimulate the release of collagen in SSc fibroblasts and induce fibrosis. Since S100A4 is essentially required for the pro-fibrotic effects of TGF-β and neutralising antibodies against S100A4 are currently evaluated, S100A4 might be a candidate for novel antifibrotic therapies.

Original language	English
Journal	Annals of the Rheumatic Diseases
Volume	74
Issue number	9
Pages (from-to)	1748-55
Number of pages	8
ISSN	0003-4967
DOIs	https://doi.org/10.1136/annrheumdis-2013-204516
Publication status	Published - 1 Sept 2015

Keywords

Adult
Aged
Animals
Disease Models, Animal
Female
Fibroblasts
Humans
Male
Mice
Mice, Knockout
Middle Aged
S100 Proteins
Scleroderma, Systemic
Skin
Smad2 Protein
Smad3 Protein
Transforming Growth Factor beta
Young Adult

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

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10.1136/annrheumdis-2013-204516

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Tomcik, M., Palumbo-Zerr, K., Zerr, P., Avouac, J., Dees, C., Sumova, B., Distler, A., Beyer, C., Cerezo, L. A., Becvar, R., Distler, O., Grigorian, M., Schett, G., Senolt, L., & Distler, J. H. W. (2015). S100A4 amplifies TGF-β-induced fibroblast activation in systemic sclerosis. Annals of the Rheumatic Diseases, 74(9), 1748-55. https://doi.org/10.1136/annrheumdis-2013-204516

Tomcik, M, Palumbo-Zerr, K, Zerr, P, Avouac, J, Dees, C, Sumova, B, Distler, A, Beyer, C, Cerezo, LA, Becvar, R, Distler, O, Grigorian, M, Schett, G, Senolt, L & Distler, JHW 2015, 'S100A4 amplifies TGF-β-induced fibroblast activation in systemic sclerosis', Annals of the Rheumatic Diseases, vol. 74, no. 9, pp. 1748-55. https://doi.org/10.1136/annrheumdis-2013-204516

@article{128f498f54a142dda356bf0e7be7394d,

title = "S100A4 amplifies TGF-β-induced fibroblast activation in systemic sclerosis",

abstract = "OBJECTIVES: S100A4 is a calcium binding protein with regulatory functions in cell homeostasis, proliferation and differentiation that has been shown to promote cancer progression and metastasis. In the present study, we evaluated the role of S100A4 in fibroblast activation in systemic sclerosis (SSc).METHODS: The expression of S100A4 was analysed in human samples, murine models of SSc and in cultured fibroblasts by real-time PCR, immunohistochemistry and western blot. The functional role of S100A4 was evaluated using siRNA, overexpression, recombinant protein and S100A4 knockout (S100A4(-/-)) mice. Transforming growth factor β (TGF-β) signalling was assessed by reporter assays, staining for phosphorylated Smad2/3 and analyses of target genes.RESULTS: The expression of S100A4 was increased in SSc skin and in experimental fibrosis in a TGF-β/Smad-dependent manner. Overexpression of S100A4 or stimulation with recombinant S100A4 induced an activated phenotype in resting normal fibroblasts. In contrast, knockdown of S100A4 reduced the pro-fibrotic effects of TGF-β and decreased the release of collagen. S100A4(-/-) mice were protected from bleomycin-induced skin fibrosis with reduced dermal thickening, decreased hydroxyproline content and lower myofibroblast counts. Deficiency of S100A4 also ameliorated fibrosis in the tight-skin-1 (Tsk-1) mouse model.CONCLUSIONS: We characterised S100A4 as a downstream mediator of the stimulatory effects of TGF-β on fibroblasts in SSc. TGF-β induces the expression of S100A4 to stimulate the release of collagen in SSc fibroblasts and induce fibrosis. Since S100A4 is essentially required for the pro-fibrotic effects of TGF-β and neutralising antibodies against S100A4 are currently evaluated, S100A4 might be a candidate for novel antifibrotic therapies.",

keywords = "Adult, Aged, Animals, Disease Models, Animal, Female, Fibroblasts, Humans, Male, Mice, Mice, Knockout, Middle Aged, S100 Proteins, Scleroderma, Systemic, Skin, Smad2 Protein, Smad3 Protein, Transforming Growth Factor beta, Young Adult",

author = "Michal Tomcik and Katrin Palumbo-Zerr and Pawel Zerr and Jerome Avouac and Clara Dees and Barbora Sumova and Alfiya Distler and Christian Beyer and Cerezo, {Lucie Andres} and Radim Becvar and Oliver Distler and Mariam Grigorian and Georg Schett and Ladislav Senolt and Distler, {J{\"o}rg H W}",

note = "Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions.",

year = "2015",

month = sep,

day = "1",

doi = "10.1136/annrheumdis-2013-204516",

language = "English",

volume = "74",

pages = "1748--55",

journal = "Annals of the Rheumatic Diseases",

issn = "0003-4967",

publisher = "B M J Group",

number = "9",

}

TY - JOUR

T1 - S100A4 amplifies TGF-β-induced fibroblast activation in systemic sclerosis

AU - Tomcik, Michal

AU - Palumbo-Zerr, Katrin

AU - Zerr, Pawel

AU - Avouac, Jerome

AU - Dees, Clara

AU - Sumova, Barbora

AU - Distler, Alfiya

AU - Beyer, Christian

AU - Cerezo, Lucie Andres

AU - Becvar, Radim

AU - Distler, Oliver

AU - Grigorian, Mariam

AU - Schett, Georg

AU - Senolt, Ladislav

AU - Distler, Jörg H W

N1 - Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions.

PY - 2015/9/1

Y1 - 2015/9/1

N2 - OBJECTIVES: S100A4 is a calcium binding protein with regulatory functions in cell homeostasis, proliferation and differentiation that has been shown to promote cancer progression and metastasis. In the present study, we evaluated the role of S100A4 in fibroblast activation in systemic sclerosis (SSc).METHODS: The expression of S100A4 was analysed in human samples, murine models of SSc and in cultured fibroblasts by real-time PCR, immunohistochemistry and western blot. The functional role of S100A4 was evaluated using siRNA, overexpression, recombinant protein and S100A4 knockout (S100A4(-/-)) mice. Transforming growth factor β (TGF-β) signalling was assessed by reporter assays, staining for phosphorylated Smad2/3 and analyses of target genes.RESULTS: The expression of S100A4 was increased in SSc skin and in experimental fibrosis in a TGF-β/Smad-dependent manner. Overexpression of S100A4 or stimulation with recombinant S100A4 induced an activated phenotype in resting normal fibroblasts. In contrast, knockdown of S100A4 reduced the pro-fibrotic effects of TGF-β and decreased the release of collagen. S100A4(-/-) mice were protected from bleomycin-induced skin fibrosis with reduced dermal thickening, decreased hydroxyproline content and lower myofibroblast counts. Deficiency of S100A4 also ameliorated fibrosis in the tight-skin-1 (Tsk-1) mouse model.CONCLUSIONS: We characterised S100A4 as a downstream mediator of the stimulatory effects of TGF-β on fibroblasts in SSc. TGF-β induces the expression of S100A4 to stimulate the release of collagen in SSc fibroblasts and induce fibrosis. Since S100A4 is essentially required for the pro-fibrotic effects of TGF-β and neutralising antibodies against S100A4 are currently evaluated, S100A4 might be a candidate for novel antifibrotic therapies.

AB - OBJECTIVES: S100A4 is a calcium binding protein with regulatory functions in cell homeostasis, proliferation and differentiation that has been shown to promote cancer progression and metastasis. In the present study, we evaluated the role of S100A4 in fibroblast activation in systemic sclerosis (SSc).METHODS: The expression of S100A4 was analysed in human samples, murine models of SSc and in cultured fibroblasts by real-time PCR, immunohistochemistry and western blot. The functional role of S100A4 was evaluated using siRNA, overexpression, recombinant protein and S100A4 knockout (S100A4(-/-)) mice. Transforming growth factor β (TGF-β) signalling was assessed by reporter assays, staining for phosphorylated Smad2/3 and analyses of target genes.RESULTS: The expression of S100A4 was increased in SSc skin and in experimental fibrosis in a TGF-β/Smad-dependent manner. Overexpression of S100A4 or stimulation with recombinant S100A4 induced an activated phenotype in resting normal fibroblasts. In contrast, knockdown of S100A4 reduced the pro-fibrotic effects of TGF-β and decreased the release of collagen. S100A4(-/-) mice were protected from bleomycin-induced skin fibrosis with reduced dermal thickening, decreased hydroxyproline content and lower myofibroblast counts. Deficiency of S100A4 also ameliorated fibrosis in the tight-skin-1 (Tsk-1) mouse model.CONCLUSIONS: We characterised S100A4 as a downstream mediator of the stimulatory effects of TGF-β on fibroblasts in SSc. TGF-β induces the expression of S100A4 to stimulate the release of collagen in SSc fibroblasts and induce fibrosis. Since S100A4 is essentially required for the pro-fibrotic effects of TGF-β and neutralising antibodies against S100A4 are currently evaluated, S100A4 might be a candidate for novel antifibrotic therapies.

KW - Adult

KW - Aged

KW - Animals

KW - Disease Models, Animal

KW - Female

KW - Fibroblasts

KW - Humans

KW - Male

KW - Mice

KW - Mice, Knockout

KW - Middle Aged

KW - S100 Proteins

KW - Scleroderma, Systemic

KW - Skin

KW - Smad2 Protein

KW - Smad3 Protein

KW - Transforming Growth Factor beta

KW - Young Adult

U2 - 10.1136/annrheumdis-2013-204516

DO - 10.1136/annrheumdis-2013-204516

M3 - Journal article

C2 - 24709861

SN - 0003-4967

VL - 74

SP - 1748

EP - 1755

JO - Annals of the Rheumatic Diseases

JF - Annals of the Rheumatic Diseases

IS - 9

ER -

S100A4 amplifies TGF-β-induced fibroblast activation in systemic sclerosis

Abstract

Keywords

UN SDGs

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