University of Hertfordshire

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Original languageEnglish
JournalBioscience Reports
Journal publication date24 Jul 2019
Publication statusAccepted/In press - 24 Jul 2019

Abstract

Vascular calcification (VC) is common in subjects with chronic kidney disease (CKD) and is associated with increased cardiovascular risk. It is an active process involving trans-differentiation of arterial smooth muscle cells (SMCs) into osteogenic phenotype. We investigated the ability of serum from CKD subjects to induce calcification in human SMCs in vitro (calcific potential of sera: CP), and associated changes in expression of RUNX2, SM22a and Klotho. Sera from subjects with CKD (18 stage 3, 17 stage 4/5, and 29 stage 5D) and 20 controls were added to human cultured SMCs and CP quantified. The CP of CKD sera was greater (p<0.01) than that of controls, though not influenced by CKD stage. MDRD-4 eGFR (p<0.001), serum phosphate (p= 0.042), RANKL (p= 0.001), PTH (p= 0.014) and HDL/Cholesterol ratio (p= 0.026) were independent predictors of CP accounting for 45% of variation. Adding calcification buffer (CB: calcium chloride [7mM] and β glycerophosphate [7mM]) increased the CP of control sera to approximate that of CKD sera. CP of CKD sera was unchanged. CKD sera increased RUNX2 expression (p<0.01) in human SMCs and decreased SM22a expression (p<0.05). Co-incubating control but not CKD serum with CB further increased RUNX2 expression (p<0.01). Both SM22a and Klotho expression decreased significantly (p<0.01) in the presence of CKD serum, and were virtually abolished with Stage 5D sera. These findings support active regulation by CKD serum of in vitro VC by induction of RUNX2 and suppression of SM22a and Klotho.

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