Abstract
We have tracked the cell surface area of CHO cells by measuring the membrane capacitance, C(m). An increase in cytosolic [Ca2+], [Ca2+](i), increased the cell surface area by 20-30%. At micromolar [Ca2+](i) the increase occurred in minutes, while at 20 μM or higher [Ca2+](i) it occurred in seconds and was transient. GTPγS caused a 3% increase even at 0.1 μM [Ca2+](i). We conclude that CHO cells, previously thought capable only of constitutive exocytosis, can perform Ca2+-triggered exocytosis that is both massive and rapid. Ca2+-triggered exocytosis was also observed in 3T3 fibroblasts. Our findings add evidence to the view that Ca induces exocytosis in cells other than known secretory cells.
Original language | English (US) |
---|---|
Pages (from-to) | 3787-3791 |
Number of pages | 5 |
Journal | EMBO Journal |
Volume | 15 |
Issue number | 15 |
DOIs | |
State | Published - Aug 1 1996 |
Externally published | Yes |
Keywords
- 3T3 fibroblasts
- Endocytosis
- Flash photolysis
- GTPγS
- Plasmalemmal repair
ASJC Scopus subject areas
- General Neuroscience
- Molecular Biology
- General Biochemistry, Genetics and Molecular Biology
- General Immunology and Microbiology