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. 2021 Aug 17;22(16):8857. doi: 10.3390/ijms22168857

Table 1.

Elemental Zinc and elemental cadmium accumulation in choroid plexus epithelial cells (CPECs) exposed for 12 h to 500 nM CdCl2 and supplemented with Zinc.

Condition Zinc, ng/mg Protein Cadmium, ng/mg Protein
Control 333.82 ± 34.04 1.02 ± 0.47
Cd 348.99 ± 42.94 265.79 ± 11.79 *
Zn 556.61 ± 53.44 * 1.14 ± 0.05
Zn + Cd 463.26 ± 15.82 * 243.72 ± 8.62 *

CPECs were first incubated for 48 h in maintenance medium without Zinc; i.e., non-supplemented cells, or with 25 µM ZnCl2; i.e., Zn-supplemented cells. Non-supplemented cells were pre-treated (12 h) in serum-free medium (SFM) and then divided into two sets: one set was exposed for 12 h in SFM with 0 CdCl2 (Control), while the other was incubated for 12 h in SFM with 500 nM CdCl2 (Cd). In parallel, Zn-supplemented cells were pre-treated (12 h) in SFM with 10 µM ZnCl2 and then divided into two sets: one set was exposed for 12 h in SFM with 10 µM ZnCl2 alone (Zn), while the other was exposed for 12 h to 500 nM CdCl2 in SFM with 10 µM ZnCl2 (Zn + Cd). All incubations were at 37 °C. Cellular content of Zn and Cd was measured by inductively coupled plasma mass spectrophotometry (ICP-MS), normalized to cell protein, and expressed as ng/mg protein. Metal accumulation was measured in duplicate in three separate culture preparations. Data are means ± SE; n = 3 culture preparations. * p < 0.05 vs. Control.