Publication Date:
2012-07-18
Description:
Disturbed transforming growth factor beta (TGFβ) signalling, leads to enhanced synthesis of extracellular matrix (ECM), which is manifested as systemic sclerosis (SSc), but this may be attenuated by the melanocortin system. Here, we report of rebound reaction in the gene expression of melanocortin receptor (MCR) subtypes and of the precursor of these receptors’ ligands, the pro-opio-melanocortin protein (POMC) in the acute skin lesion of diffuse systemic sclerosis (dSSc) after treatment with a recombinant human anti- TGFβ1 antibody. Biopsies, taken from the leading edge of the skin lesion, before and after treatment of a patient with recent onset dSSc, were examined. Before treatment, increased levels of TGFβ mRNA and suppressed levels of POMC mRNA and melanocortin receptor subtypes MC 1-3, 5 R mRNAs were seen in the lesion, compared with healthy controls. After treatment, there was a rebound expression of POMC, MC 2, 3, 5 R mRNAs. As the melanocortin system regulates collagen and melanin production, our findings add a new understanding to the pathogenetic mechanisms involved in the acute skin lesion of dSSc, which is characterized by enhanced ECM formation and changes in skin pigmentation.
Print ISSN:
0300-9475
Electronic ISSN:
1365-3083
Topics:
Medicine
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