Abstract
Aim: To characterize Ca2+-stimulated exocytosis in isolated mouse pancreatic β cells. Methods: An improved method was described for isolation of mouse pancreatic β cells by collagenase P. The Ca2+ channel current and the membrane capacitance were examined by using the whole-cell patch clamp recording technique. Results: Using depolarization and flash photolysis of caged Ca2+ to induce Ca2+-dependent exocytosis in β cell from KM mouse, we have explored the characteristics of the Ca2+ channel current and the relationship between Ca 2+ signals and exocytosis. The averaged peak Ca2+ current measured at +20 mV was -60±6 pA (n= 13). Conclusion: We characterized three kinetically different pools of vesicles in mouse pancreatic β cells, namely an immediately releasable pool, a readily releasable pool, and a reserve pool. ©2006 CPS and SIMM.
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Ge, Q., Dong, Y. M., Hu, Z. T., Wu, Z. X., & Xu, T. (2006). Characteristics of Ca2+-exocytosis coupling in isolated mouse pancreatic β cells. Acta Pharmacologica Sinica, 27(7), 933–938. https://doi.org/10.1111/j.1745-7254.2006.00398.x
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