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Membrane proximal lysosomes are the major vesicles responsible for calcium-dependent exocytosis in nonsecretory cells
Open accessAbstract
Similar to its role in secretory cells, calcium triggers exocytosis in nonsecretory cells. This calcium-dependent exocytosis is essential for repair of membrane ruptures. Using total internal reflection fluorescence microscopy, we observed that many organelles implicated in this process, including ER, post-Golgi vesicles, late endosomes, early endosomes, and lysosomes, were within 100 nm of the plasma membrane (in the evanescent field). However, an increase in cytosolic calcium led to exocytosis of only the lysosomes. The lysosomes that fused were predominantly predocked at the plasma membrane, indicating that calcium is primarily responsible for fusion and not recruitment of lysosomes to the cell surface.
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Verkhratsky, A., & Nedergaard, M. (2018) · Physiological Reviews · doi:10.1152/physrev.00042.2016 · Cited by 1,678
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Metadata
- Authors
- Jaiswal, J. K., Andrews, N. W., & Simon, S. M.
- Venue
- The Journal of Cell Biology
- Publisher
- Rockefeller University Press
- Published
- 2002-11-18
- Volume
- 159
- Issue
- 4
- Pages
- 625-635
- ISSN
- 0021-9525 (ISSN-L)
- 1540-8140
- OpenAlex
- W2142142736
- Cited by
- 386
- References
- 0
- FWCI
- 4.91
- Type
- journal article
- Language
- en
- Open access
- green
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