Effect of Replacing Extracellular Ca2+With EGTA on Dense Cell Formation
Condition (n = 4) . | % Cells After 22 Hours of O-D Cycling . | |||
---|---|---|---|---|
LD . | ND . | ID . | HD . | |
0.5 mmol/L Ca2+ | 6 ± 2 | 32 ± 24 | 38 ± 26 | 24 ± 8 |
0.5 mmol/L EGTA | 7 ± 3 | 33 ± 20 | 51 ± 13 | 9 ± 8 |
p < .043v Ca2+ |
Condition (n = 4) . | % Cells After 22 Hours of O-D Cycling . | |||
---|---|---|---|---|
LD . | ND . | ID . | HD . | |
0.5 mmol/L Ca2+ | 6 ± 2 | 32 ± 24 | 38 ± 26 | 24 ± 8 |
0.5 mmol/L EGTA | 7 ± 3 | 33 ± 20 | 51 ± 13 | 9 ± 8 |
p < .043v Ca2+ |
SS-ND cells were O-D cycled for 22 hours at pH 6.8 in buffer containing physiologic levels of Cl−, after which the cells were separated using continuous density gradients and quantitated, as in Fig 1. LD, <1.080 g/mL; ND, 1.080 to 1.090 g/mL; ID, 1.090 to 1.114 g/mL; HD, >1.114 g/mL.