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Originally published as MBC in Press, 10.1091/mbc.E05-05-0382 on November 28, 2005

Vol. 17, Issue 2, 711-722, February 2006

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SNAP25, but Not Syntaxin 1A, Recycles via an ARF6-regulated Pathway in Neuroendocrine Cells

Yoshikatsu Aikawa, Xiaofeng Xia, and Thomas F.J. Martin

Department of Biochemistry, University of Wisconsin, Madison, WI 53706

Submitted May 3, 2005; Accepted November 14, 2005
Monitoring Editor: Keith Mostov

Soluble N-ethylmaleimide-sensitive fusion protein attachment protein receptor (SNARE) proteins mediate cellular membrane fusion events and provide a level of specificity to donor–acceptor membrane interactions. However, the trafficking pathways by which individual SNARE proteins are targeted to specific membrane compartments are not well understood. In neuroendocrine cells, synaptosome-associated protein of 25 kDa (SNAP25) is localized to the plasma membrane where it functions in regulated secretory vesicle exocytosis, but it is also found on intracellular membranes. We identified a dynamic recycling pathway for SNAP25 in PC12 cells through which plasma membrane SNAP25 recycles in ~3 h. Approximately 20% of the SNAP25 resides in a perinuclear recycling endosome–trans-Golgi network (TGN) compartment from which it recycles back to the plasma membrane. SNAP25 internalization occurs by constitutive, dynamin-independent endocytosis that is distinct from the dynamin-dependent endocytosis that retrieves secretory vesicle constituents after exocytosis. Endocytosis of SNAP25 is regulated by ADP-ribosylation factor (ARF)6 (through phosphatidylinositol bisphosphate synthesis) and is dependent upon F-actin. SNAP25 endosomes, which exclude the plasma membrane SNARE syntaxin 1A, merge with those derived from clathrin-dependent endocytosis containing endosomal syntaxin 13. Our results characterize a robust ARF6-dependent internalization mechanism that maintains an intracellular pool of SNAP25, which is compatible with possible intracellular roles for SNAP25 in neuroendocrine cells.


This article was published online ahead of print in MBC in Press (http://www.molbiolcell.org/cgi/doi/10.1091/mbc.E05–05–0382) on November 28, 2005.

Abbreviations used: ARF, ADP-ribosylation factor; BFA, brefeldin A; CHX, cycloheximide; CTxB, cholera toxin B; FRAP, fluorescence recovery after photobleaching; GFP, green fluorescent protein; PBS, phosphate-buffered saline; PIP2, phosphatidylinositol(4,5)bisphosphate; PI(4)P 5-kinase I, phosphatidylinositol(4)phosphate 5-kinase type I; SNAP25, synaptosome-associated protein of 25 KDa; SNARE, soluble N-ethylmaleimide-sensitive factor attachment protein receptor; Tf, transferrin.

Address correspondence to: Thomas F.J. Martin (tfmartin{at}facstaff.wisc.edu).




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