Vol.23 No.3

Original Article

Scleroderma dermal fibroblasts overexpress vascular endothelial growth factor due to autocrine transforming growth factor b signaling

Authors

Ikko Kajihara¹ , Masatoshi Jinnin¹ , Noritoshi Honda¹ , Katsunari Makino¹ , Takamitsu Makino¹ , Shinichi Masuguchi¹ , Keisuke Sakai¹ , Satoshi Fukushima¹ , Yuji Inoue¹ , Hironobu Ihn¹

Received:

8 March 2012

Accepted:

5 June 2012

Published online:

28 June 2012

Full Text

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Abstract

Objectives Overexpression of vascular endothelial growth factor (VEGF) in scleroderma (SSc) skin may play a role in the pathogenesis of the disease. Our study was undertaken to evaluate whether dermal fibroblasts function as one of the sources of the increased VEGF in SSc, and to clarify its mechanism.
Methods Protein and mRNA levels of VEGF were analyzed using immunoblotting, enzyme-linked immunosorbent
assay, and real-time PCR. The DNA-binding ability of Smad3 was evaluated by DNA affinity precipitation.
Results VEGF mRNA expression in vivo was increased in SSc skin compared to skin with other collagen diseases. Expression of VEGF protein and mRNA in cultured SSc dermal fibroblasts was constitutively and significantly upregulated. Ectopic TGF-b stimulation induced VEGF synthesis in normal fibroblasts, and TGF-b knockdown normalized the upregulated VEGF levels in SSc fibroblasts. Furthermore, Smad3 overexpression induced VEGF levels. We found that bp -532 to -521 on the VEGF promoter is a putative binding site for Smads, and that the binding activity of Smad3 to VEGF promoter was constitutively increased in SSc fibroblasts as well as in normal fibroblasts treated with exogenous TGF-b1.
Conclusions We demonstrated that VEGF were overexpressed due to autocrine TGF-b/Smad signaling in SSc. TGF-b signaling may contribute to the pathogenesis of angiopathy as well as tissue fibrosis.

Key words

Angiogenesis, Fibrosis, Extracellular matrix