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Patients with end-stage renal disease (ESRD) have elevated circulating calcium (Ca) and phosphate (Pi), and exhibit accelerated progression of calcific aortic valve disease (CAVD). We hypothesized that matrix vesicles (MVs) initiate the calcification process in CAVD. Ca induced rat valve interstitial cells (VICs) calcification at 4.5 mM (16.4-fold; p 

Original publication

DOI

10.1002/jcp.25935

Type

Journal article

Journal

J cell physiol

Publication Date

11/2017

Volume

232

Pages

2985 - 2995

Keywords

Annexin VI, calcific aortic valve disease, calcification, matrix vesicles, Aged, Alkaline Phosphatase, Animals, Annexin A6, Aortic Valve, Aortic Valve Stenosis, Calcinosis, Calcium, Cells, Cultured, Core Binding Factor Alpha 1 Subunit, Extracellular Matrix, Extracellular Vesicles, Female, Homeodomain Proteins, Humans, Hypercalcemia, Kidney Failure, Chronic, Male, Microscopy, Electron, Transmission, Protein Interaction Maps, Proteomics, RNA, Messenger, Rats, Sprague-Dawley, Up-Regulation