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Fli1 deficiency contributes to the suppression of endothelial CXCL5 expression in systemic sclerosis

CXCL5 is a member of CXC chemokines with neutrophilic chemoattractant and pro-angiogenic properties, which has been implicated in the pathological angiogenesis of rheumatoid arthritis and inflammatory bowel diseases. Since aberrant angiogenesis is also involved in the developmental process of system...

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Bibliographic Details
Published in:Archives of Dermatological Research 2014-05, Vol.306 (4), p.331-338
Main Authors: Ichimura, Yohei, Asano, Yoshihide, Akamata, Kaname, Takahashi, Takehiro, Noda, Shinji, Taniguchi, Takashi, Toyama, Tetsuo, Aozasa, Naohiko, Sumida, Hayakazu, Kuwano, Yoshihiro, Yanaba, Koichi, Tada, Yayoi, Sugaya, Makoto, Sato, Shinichi, Kadono, Takafumi
Format: Article
Language:English
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Summary:CXCL5 is a member of CXC chemokines with neutrophilic chemoattractant and pro-angiogenic properties, which has been implicated in the pathological angiogenesis of rheumatoid arthritis and inflammatory bowel diseases. Since aberrant angiogenesis is also involved in the developmental process of systemic sclerosis (SSc), we herein measured serum CXCL5 levels in 63 SSc and 18 healthy subjects and investigated their clinical significance and the mechanism explaining altered expression of CXCL5 in SSc. Serum CXCL5 levels were significantly lower in SSc patients than in healthy subjects. In diffuse cutaneous SSc (dcSSc), serum CXCL5 levels were uniformly decreased in early stage (
ISSN:0340-3696
1432-069X
DOI:10.1007/s00403-013-1431-9