Inorganic Phosphate Stimulates Fibronectin Expression in Renal Fibroblasts

被引:19
作者
Chen, Zhonghai
Chen, Dong
McCarthy, Thomas L. [2 ]
Centrella, Michael [2 ]
Zhang, Yuning
Moeckel, Gilbert W. [1 ]
机构
[1] Yale Univ, Sch Med, Dept Patol, Renal Pathol Lab, New Haven, CT 06520 USA
[2] Yale Univ, Sch Med, Dept Surg, New Haven, CT 06520 USA
关键词
Fibroblast; Akt; Osterix; Fibronectin; NFATc1; c-fos; OSTEOBLAST DIFFERENTIATION; TRANSCRIPTION FACTOR; BONE-FORMATION; RISK-FACTOR; CELLS; OSTERIX; FAILURE; DISEASE; GENE; HYPERPHOSPHATEMIA;
D O I
10.1159/000339054
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Elevated plasma phosphate levels are signifcantly associated with progression of chronic kidney disease (CKD). Interstitial fibrosis is an important factor in the progression of CKD. In this study we investigate the role of inorganic phosphate in stimulating fibronectin (FN) synthesis in a kidney fibroblast cell line (NRK-49F). We find that phosphate increases FN abundance and message in a dose dependent fashion and that both ERK1/2 and AKT are important signaling pathways that mediate phosphate-dependent FN expression in NRK-49F cells. Moreover phosphate stimulates the expression of the transcription factors osterix and NFATc1, which form complexes and mediate FN synthesis. Another transcription factor involved in phosphate-dependent FN synthesis is the AP1 family member c-Fos. In summary we show that even mildly elevated serum phosphate levels can induce synthesis of the interstitial matrix protein fibronectin through activation of ERK1/2 and AKT signaling pathways in kidney fibroblasts and that the synthesis of fibronectin is mediated by a transcriptional complex consisting of NFATc1, osterix and c-Fos. Copyright (c) 2012 S. Karger AG, Basel
引用
收藏
页码:151 / 159
页数:9
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