Abstract

Biologic nanoparticles (NPs) ‐ protein/mineral complexes isolatable from human calcified, but not uncalcified arteries and from plasma ‐ propagate and accumulate calcium phosphate when in cell culture conditions. IV injection of NPs into animals results in vascular calcification at sites of endothelial injury. Our aim was to determine if NPs promote mineralization by localizing to vascular smooth muscle cells (VSMCs), then sequestering calcium from their environment. Porcine VSMCs were cultured in 24‐well plates to sub‐confluency (day 0). 45Ca (1 μCi/well) to label deposited mineral was added to media containing vehicle (control), NPs (10 or 100 nephelometric turbidity units; NTU; average diameter 210 nm), or 2 mM Pi (positive‐control). After 15 days, VSMCs formed multicellular nodules. VSMCs in control media were negative for calcification by von Kossa staining; whereas micron‐sized to smaller particles stained positive for calcium in nodules from NP‐treated and Pi‐treated cells. Cells treated identically were demineralized with 0.6N HCl and the liberated 45Ca was quantified by scintillation counting. CPM/well (x103) were 1.5 in controls and 4.6, 28.2 and 64.7 in cells treated with 10 NTU NPs, Pi, and 100 NTU NPs, respectively. NPs localize to VSMCs in vitro and promote mineralization through sequestration of Ca from the environment. (Supported by NIH grant HL88988, and Mayo Clinic).

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