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Spatial and Temporal Aspects of Exocytosis Studied on the Isolated Plasma Membranes. | LitMetric

AI Article Synopsis

  • Exocytosis in neuroendocrine cells involves a complex, calcium-based mechanism regulated by proteins and lipids.
  • The described experimental method uses adrenal chromaffin cells and ultrasonic pulses to create thin plasma membranes with secretory vesicles for studying exocytosis.
  • This assay is effective for analyzing secretion and detecting various proteins and lipids, providing good spatial resolution while being simple, quick, and cost-effective.

Article Abstract

Exocytosis of large-dense core vesicles in neuroendocrine cells is a highly regulated, calcium-dependent process, mediated by networks of interrelated proteins and lipids. Here, I describe experimental procedures for studies of selective spatial and temporal aspects of exocytosis at the plasma membrane, or in its proximity, using adrenal chromaffin cells. The assay utilizes primary cells subjected to a brief ultrasonic pulse, resulting in the formation of thin, flat inside-out plasma membranes with attached secretory vesicles and elements of cell cytoskeleton. In this model, secretion of plasma membrane-attached secretory vesicles was found to be dependent on calcium and sensitive to clostridial neurotoxins. Depending on the probe selected for secretory vesicle cargo, protein, and/or lipid detection, this simple assay is versatile, fast and inexpensive, and offers excellent spatial resolution.

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Source
http://dx.doi.org/10.1007/978-1-0716-1044-2_21DOI Listing

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