Dr. Silver is in the Departments of Pharmacology, Physiology, and Radiology, School of Medicine, Department of Biomedical Engineering, and College of Engineering at Wayne State University, Detroit, MI. He also holds appointments at the John D. Dingell VA Medical Center, Detroit, MI, and the Decision and Information Sciences Division, Argonne National Laboratory, Argonne, IL.
Feature article
Secretion without membrane fusion: Porocytosis
Article first published online: 25 JAN 2005
DOI: 10.1002/ar.b.20050
Copyright © 2005 Wiley-Liss, Inc.
Issue

The Anatomical Record Part B: The New Anatomist
Volume 282B, Issue 1, pages 18–37, January 2005
Additional Information
How to Cite
Silver, R. B. and Pappas, G. D. (2005), Secretion without membrane fusion: Porocytosis. Anat. Rec., 282B: 18–37. doi: 10.1002/ar.b.20050
Publication History
- Issue published online: 25 JAN 2005
- Article first published online: 25 JAN 2005
Funded by
- NSF MCB. Grant Number: 9602056
- U.S. Department of Veterans Affairs
- National Institutes of Health. Grant Number: DA 01551
- Abstract
- Article
- References
- Cited By
Keywords:
- vesicular secretion;
- constitutive secretion;
- porocytosis;
- quantal release;
- SNARE;
- membrane fusion;
- plasma membrane
Abstract
We have recently proposed a mechanism to describe secretion, a fundamental process in all cells. That hypothesis, called porocytosis, embodies all available data and encompasses both forms of secretion, i.e., vesicular and constitutive. The current accepted view of exocytotic secretion involves the physical fusion of vesicle and plasma membranes; however, that hypothesized mechanism does not fit all available physiological data. Energetics of apposed lipid bilayers do not favor unfacilitated fusion. We consider that calcium ions (e.g., 10−4 to 10−3 M calcium in microdomains when elevated for 1 ms or less), whose mobility is restricted in space and time, establish salt bridges among adjacent lipid molecules. This establishes transient pores that span both the vesicle and plasma membrane lipid bilayers; the diameter of this transient pore would be ∼ 1 nm (the diameter of a single lipid molecule). The lifetime of the transient pore is completely dependent on the duration of sufficient calcium ion levels. This places the porocytosis hypothesis for secretion squarely in the realm of the physical and physical chemical interactions of calcium and phospholipids and places mass action as the driving force for release of secretory material. The porocytosis hypothesis that we propose satisfies all of the observations and provides a framework to integrate our combined knowledge of vesicular and constitutive secretion. Anat Rec (Part B: New Anat) 282B:18–37, 2005. © 2005 Wiley-Liss, Inc.

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