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Localization of fibroblast growth factor-2 (basic FGF) and FGF receptor-1 in adult human kidney11See Editorial by Barasch, p. 1156

Authors :
Floege, Jürgen
Hudkins, Kelly L.
Eitner, Frank
Cui, Yan
Morrison, Richard S.
Schelling, Margaret A.
Alpers, Charles E.
Source :
Kidney International. 56(3):883-897
Publication Year :
1999
Publisher :
Elsevier BV, 1999.

Abstract

Localization of fibroblast growth factor-2 (basic FGF) and FGF receptor-1 in adult human kidney.BackgroundThe expression pattern of fibroblast growth factor-2 (FGF-2; basic FGF), a pleiotrophic growth factor, as well as one of its receptors (FGFR1), in the kidney is highly controversial.MethodsUsing an approach that combines multiple antibodies for immunohistochemistry and correlative in situ hybridization, we assessed the intrarenal expression of both FGF-2 and FGFR1 in 13 specimens of adult kidney removed during tumor nephrectomy.ResultsThe FGF-2 expression pattern in the kidneys as detected by immunohistochemistry was variable and depended on the antibody used. The most consistent expression of FGF-2 protein was demonstrated in glomerular parietal epithelial cells, tubular cells (mainly of the distal nephron), as well as arterial endothelial cells. These locations also corresponded to areas of FGF-2 mRNA expression. Additionally, by immunohistochemistry, FGF-2 protein was detected in arterial smooth muscle cells and occasional podocytes. The expression of FGFR1 protein and mRNA was most consistently present in tubular cells of the distal nephron and in vascular smooth muscle cells. In situ hybridization, but not immunohistochemistry, also suggested FGFR1 expression in cells that could not be precisely identified within the glomerular tuft as well as some interstitial cells.ConclusionThese data suggest potential autocrine and paracrine pathways within the FGF-2 system, particularly within the vascular walls and in the distal nephron, and thereby provide information for further mechanistic understanding of the role of the FGF-2 system in human renal disease.

Details

ISSN :
00852538
Volume :
56
Issue :
3
Database :
OpenAIRE
Journal :
Kidney International
Accession number :
edsair.dedup.wf.001..f062605d7716d157c024340bdea3f0cf
Full Text :
https://doi.org/10.1046/j.1523-1755.1999.00637.x