Function of the t-SNARE SNAP-23 and secretory carrier membrane proteins (SCAMPs) in exocytosis in mast cells

J. David Castle, Zhenheng Guo, Lixia Liu

Research output: Contribution to journalReview articlepeer-review

40 Scopus citations


Mast cells acutely respond to allergens and other stimuli by releasing accumulated internal stores of inflammatory mediators and other secretory products by "compound" exocytosis involving massive granule-to-plasma membrane and granule-to-granule fusion. Our recent findings implicate the SNAP receptor (SNARE) protein SNAP-23 and secretory carrier membrane protein 2 (SCAMP2) as regulators of this process. We summarize evidence indicating that stimulus-induced relocation of SNAP-23 from foci in the plasma membrane to putative sites of membrane fusion both at the cell surface and intracellularly between granules is an essential link in coupling stimulation to exocytosis. We also review recent findings showing that the candidate exocytotic SNAREs SNAP-23 and syntaxin 4 colocalize with SCAMPs, especially SCAMP2, and that SCAMP2 is likely to be a partner in the compound exocytotic process.

Original languageEnglish
Pages (from-to)1337-1340
Number of pages4
JournalMolecular Immunology
Issue number16-18
StatePublished - 2002

Bibliographical note

Funding Information:
We are very grateful to Dr. Anna Castle and Dr. Sam Green for advice and discussion throughout these studies. Our work has been supported by NIH grants DE09655 and AI 47150.


  • Exocytosis
  • Membrane fusion
  • Membrane proteins
  • SNAREs

ASJC Scopus subject areas

  • Immunology
  • Molecular Biology


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