Phosphate uptake-independent signaling functions of the type III sodium-dependent phosphate transporter, PiT-1, in vascular smooth muscle cells.

Autor: Chavkin NW; Department of Bioengineering, University of Washington, Box 355061, Foege Hall Seattle, WA 98195, USA., Chia JJ; Department of Bioengineering, University of Washington, Box 355061, Foege Hall Seattle, WA 98195, USA., Crouthamel MH; Department of Bioengineering, University of Washington, Box 355061, Foege Hall Seattle, WA 98195, USA., Giachelli CM; Department of Bioengineering, University of Washington, Box 355061, Foege Hall Seattle, WA 98195, USA. Electronic address: ceci@uw.edu.
Jazyk: angličtina
Zdroj: Experimental cell research [Exp Cell Res] 2015 Apr 10; Vol. 333 (1), pp. 39-48. Date of Electronic Publication: 2015 Feb 13.
DOI: 10.1016/j.yexcr.2015.02.002
Abstrakt: Vascular calcification (VC) is prevalent in chronic kidney disease and elevated serum inorganic phosphate (Pi) is a recognized risk factor. The type III sodium-dependent phosphate transporter, PiT-1, is required for elevated Pi-induced osteochondrogenic differentiation and matrix mineralization in vascular smooth muscle cells (VSMCs). However, the molecular mechanism(s) by which PiT-1 promotes these processes is unclear. In the present study, we confirmed that the Pi concentration required to induce osteochondrogenic differentiation and matrix mineralization of mouse VSMCs was well above that required for maximal Pi uptake, suggesting a signaling function of PiT-1 that was independent of Pi transport. Elevated Pi-induced signaling via ERK1/2 phosphorylation was abrogated in PiT-1 deficient VSMCs, but could be rescued by wild-type (WT) and a Pi transport-deficient PiT-1 mutant. Furthermore, both WT and transport-deficient PiT-1 mutants promoted osteochondrogenic differentiation as measured by decreased SM22α and increased osteopontin mRNA expression. Finally, compared to vector alone, expression of transport-deficient PiT-1 mutants promoted VSMC matrix mineralization, but not to the extent observed with PiT-1 WT. These data suggest that both Pi uptake-dependent and -independent functions of PiT-1 are important for VSMC processes mediating vascular calcification.
(Copyright © 2015 Elsevier Inc. All rights reserved.)
Databáze: MEDLINE
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