Tropoelastin regulates chemokine expression in fibroblasts in Costello syndrome

Costello syndrome is a multiple congenital anomaly associated with growth and mental retardation, cardiac and skeletal anomalies, and a predisposition to develop neoplasia. Comprehensive expression analysis revealed remarkable up-regulation of several cytokines and chemokines including Gro family pr...

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Veröffentlicht in:Biochemical and biophysical research communications 2008-08, Vol.372 (4), p.681-687
Hauptverfasser: Tatano, Yutaka, Fujinawa, Reiko, Kozutsumi, Yasunori, Takahashi, Tsutomu, Tsuji, Daisuke, Takeuchi, Naohiro, Tsuta, Kohji, Takada, Goro, Sakuraba, Hitoshi, Itoh, Kohji
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Sprache:eng
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Zusammenfassung:Costello syndrome is a multiple congenital anomaly associated with growth and mental retardation, cardiac and skeletal anomalies, and a predisposition to develop neoplasia. Comprehensive expression analysis revealed remarkable up-regulation of several cytokines and chemokines including Gro family proteins, interleukin-1β (IL-1β), IL-8 and MCP-1 but down-regulation of extracellular matrix components including collagens and proteoglycans of skin fibroblasts derived from a Japanese Costello syndrome patient characterized by significantly reduced tropoelastin mRNA, impaired elastogenesis and enhanced cell proliferation. In contrast, decreases in these chemokines and IL-1β expression were observed in Costello fibroblastic cell lines stably expressing the bovine tropoelastin (btEln) gene and in restored elastic fibers. These results strongly suggest that the human TE gene ( ELN) transfer could be applicable for the gene therapy of a group of Costello syndrome patients with reduced ELN gene expression.
ISSN:0006-291X
1090-2104
DOI:10.1016/j.bbrc.2008.05.131