Calcitonin induces connective tissue growth factor through ERK1/2 signaling in renal tubular cells

被引:0
作者
Misa Nakamura
Takashi Ozaki
Aiko Ishii
Masayoshi Konishi
Yuji Tsubota
Toru Furui
Hayato Tsuda
Ichiro Mori
Kiichiro Ota
Kennichi Kakudo
机构
[1] Wakayama Medical University,Department of Pathology
[2] Wakayama 641-0012,Department of Rehabilitation
[3] Japan.,undefined
[4] Osaka Kawasaki Rehabilitation University,undefined
[5] Osaka 597-0104,undefined
[6] Japan.,undefined
来源
Experimental & Molecular Medicine | 2009年 / 41卷
关键词
calcitonin; connective tissue growth factor; extracellular signal-regulated MAP kinases; gene expression regulation; kidney; wound healing;
D O I
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中图分类号
学科分类号
摘要
Calcitonin (CT), a polypeptide hormone, plays important roles in a variety of physiological processes. CT has been used clinically to treat osteoporosis and humoral hypercalcemia of malignancy. In order to clarify the pharmacological effects of CT in the kidney, we identified potential downstream genes induced by CT in the renal cells. Using a cDNA subtraction hybridization method, we identified connective tissue growth factor (CTGF) as a CT-induced gene in the porcine renal cell line, LLC-PK1. Furthermore, we found that CT-mediated induction of the gene was not inhibited by cycloheximide, which suggests that CTGF gene was not induced by an increased synthesis of regulating proteins. Therefore, CTGF is an immediate early gene. We further demonstrated that the regulation of CTGF gene expression by CT involved the ERK1/2 pathway, because PD98059, a MEK1 inhibitor, partially inhibited the mRNA expression of CTGF induced by CT. CT-induced CTGF protein expression was also observed in vivo. Our present findings suggest that CT induces the transcription of CTGF through ERK1/2 phosphorylation. We also identified twelve other genes induced by CT that, like CTGF, were related to wound healing. These results suggest that CT may have an effect on renal differentiation and wound healing in the kidney.
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页码:307 / 314
页数:7
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