45Ca2+ uptake study in PC12 cells

<center> <h3> 45Ca2+ uptake study in PC12 cells</h3> </center>

 

1. Plate the cells on to the poly-D-Lysine-coated six well plates 2 days prior to study. 

2. Rinse the cells with 1 ml secretion buffer (150 mM NaCl, 5mM KCl, 2mM CaCl2, 10 mM Hepes, pH 7.4) every 15 minutes for 1 hour at 37^o C. 

3. Add 45Ca2+ (2 µCi/ml) to Ca2+ -free buffer (secretion buffer without 2 mM CaCl2), and drugs to the labelled buffer at 37^o C. 

4. Incubate the cells with labelled buffer with different conditions for 1 minute at room temperature. 

5. After 1 minute dump the solution and add 2 ml of ice cold Ca2+ -free buffer with 2 mM LaCl3 and 2 mM EGTA. 

6. Wash the cells 6 times with ice cold Ca2+ -free buffer with LaCl3 and EGTA. 

7. Add 1 ml of cell lysis buffer to each well. 

8. Collect the cell lysate after 30 minutes and count in a beta-counter using 

program for 14C. 

9. The data are expressed as dpm/well. 

Source of the reagents: 45Ca2+ (Dupont) (Calcium chloride in water; specific activity: 25.92 mCi/mg).