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. 2014 May 21;9(5):e97565. doi: 10.1371/journal.pone.0097565

Table 2. Cytotoxic effects of CaP particles in the presence or absence of fetuin-A or albumin or functionalised CaP particles (CaP with fetuin-A attached, CaP/F or with albumin attached, CaP/A) on fura-2 loaded VSMCs.

Dead cells/total cells % death n
Control (no CaP) 0/80 0 15
CaP 82/102 80 17
CaP+fetuin-A (1 µM) 1/27 4 4
CaP+fetuin-A (0.1 µM) 19/22 86 4
CaP+albumin (1 µM) 1/21 5 4
CaP+albumin (0.1 µM) 18/23 78 4
CaP/F 9/49 18 8
CaP/A 14/16 88 3

Stock concentrations of particles contained 2.9 mg/mL Ca2+ for CaP, 0.8 mg/mL Ca2+ for CaP/F and 1.84 mg/mL Ca2+ for CaP/A. The particle concentration used in each experiment was 25 µg/mL in terms of Ca2+ content. Samples were prepared as a 250 µg/mL solution in 100 µl physiological buffer and added to VSMCs in a chamber containing 900 µl physiological buffer. All particle solutions were vortexed immediately prior to addition to cells. Raw data are presented, i.e. 82/102 denotes that 82 out of 102 cells that were imaged died within 1 hour of an experiment. Cell death was determined by fura-2 leak from cells. ‘n’ represents the number of separate experiments. Representative Ca2+ traces are shown in figure 2 and figures S2, S4 and S5.