Fibroblast growth factor receptors and their ligands in the adult rat kidney

Citation
B. Cancilla et al., Fibroblast growth factor receptors and their ligands in the adult rat kidney, KIDNEY INT, 60(1), 2001, pp. 147-155
Citations number
56
Categorie Soggetti
Urology & Nephrology","da verificare
Journal title
KIDNEY INTERNATIONAL
ISSN journal
00852538 → ACNP
Volume
60
Issue
1
Year of publication
2001
Pages
147 - 155
Database
ISI
SICI code
0085-2538(200107)60:1<147:FGFRAT>2.0.ZU;2-Q
Abstract
Background. Fibroblast growth factors (FGFs) are a family of at least 21 he parin-binding proteins involved in many biological processes, both during d evelopment and in the adult, including cell proliferation, differentiation, and angiogenesis. FGFs mediate their effects through high-affinity tyrosin e kinase receptors (FGFRs), which are encoded by four genes. The aims of th e present study were to localize FGFR-1 through FGFR-3 in the normal adult rat kidney and to determine which functional FGFR variants and FGFs were ex pressed. Methods. Avidin-biotin-enhanced horseradish peroxidase immunohistochemistry was used on paraffin sections of rat kidney to localize FGFR-1 through FGF R-3, whereas reverse transcriptase-polymerase chain reaction was used to ex amine expression of the receptor variants and also of FGF-1 through FGF-10 in cortex, outer medulla, and inner medulla. Results. By immunohistochemistry, each receptor was localized to distinct a nd overlapping nephron segments, such that one or more FGFRs were localized to all nephron and collecting duct epithelia. FGFR-1 and FGFR-3 were local ized to glomeruli, FGFR-3 to proximal tubules and FGFR-1 to thin limbs. FGF R-1 through FGFR-3 were localized to distal straight tu bules, with FGFR-1 and FGFR-3 localized to distal convoluted tubules. FGFR-1 and FGFR-3 were l ocalized to medullary collecting ducts. in addition, FGFR-1 was localized t o the smooth muscle of renal arteries. All seven FGFR variants were express ed in the cortex and outer medulla, with fewer FGFRs in the inner medulla. FGF-1, FGF-2, FGF-7, FGF-8, and FGF-9 were expressed in the kidney, with FG F-IO expression found only in the cortex. Conclusions. Mapping of these receptors is critical to the determination of the effects of FGF ligands in discrete regions of the kidney. The distribu tions of the FGFRs in the normal adult kidney and the restricted expression of FGF ligands suggest that specific FGFs have distinct and important role s in the maintenance of normal kidney structure and function.