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Publication : Cardiovascular Effects of Renal Distal Tubule Deletion of the FGF Receptor 1 Gene.

First Author  Han X Year  2018
Journal  J Am Soc Nephrol Volume  29
Issue  1 Pages  69-80
PubMed ID  28993502 Mgi Jnum  J:291066
Mgi Id  MGI:6435959 Doi  10.1681/ASN.2017040412
Citation  Han X, et al. (2018) Cardiovascular Effects of Renal Distal Tubule Deletion of the FGF Receptor 1 Gene. J Am Soc Nephrol 29(1):69-80
abstractText  The bone-derived hormone fibroblast growth factor-23 (FGF-23) activates complexes composed of FGF receptors (FGFRs), including FGFR1, and alpha-Klotho in the kidney distal tubule (DT), leading to increased sodium retention and hypertension. However, the role of FGFR1 in regulating renal processes linked to hypertension is unclear. Here, we investigated the effects of selective FGFR1 loss in the DT. Conditional knockout (cKO) of FGFR1 in the DT (FGFR1(DT-cKO) mice) resulted in left ventricular hypertrophy (LVH) and decreased kidney expression of alpha-Klotho in association with enhanced BP, decreased expression of angiotensin converting enzyme 2, and increased expression of the Na(+)-K(+)-2Cl(-) cotransporter. Notably, recombinant FGF-23 administration similarly decreased the kidney expression of alpha-Klotho and induced LVH in mice. Pharmacologic activation of FGFR1 with a monoclonal anti-FGFR1 antibody (R1MAb1) normalized BP and significantly attenuated LVH in the Hyp mouse model of excess FGF-23, but did not induce a response in FGFR1(DT-cKO) mice. The hearts of FGFR1(DT-cKO) mice showed increased expression of the transient receptor potential cation channel, subfamily C, member 6 (TRPC6), consistent with cardiac effects of soluble Klotho deficiency. Moreover, administration of recombinant soluble Klotho lowered BP in the Hyp mice. Thus, FGFR1 in the DT regulates systemic hemodynamic responses opposite to those predicted by the actions of FGF-23. These cardiovascular effects appear to be mediated by paracrine FGF control of kidney FGFR1 and subsequent regulation of soluble Klotho and TRPC6. FGFR1 in the kidney may provide a new molecular target for treating hypertension.
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