4.6 Article

Real-time imaging of mast cell degranulation in vitro and in vivo

Journal

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.bbrc.2016.09.100

Keywords

Mast cell; Degranulation; Exocytosis; pH sensor; VAMP-8; Imaging

Funding

  1. JST
  2. Japanese Ministry of Education, Culture, Sports, Science and Technology [15H05786]
  3. Urakami foundation for Food and Food Culture Promotion
  4. Sasakawa foundation
  5. Grants-in-Aid for Scientific Research [15K20969, 15H05786] Funding Source: KAKEN

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Mast cells undergo degranulation in response to various stimuli and rapidly release pre-formed mediators present in secretory granules, leading to immediate-type allergic reactions. Mast cell degranulation is commonly detected and quantified in vitro by measuring histamine or beta-hexosaminidase released to culture medium. However, this type of assay cannot monitor degranulation of individual cells in real time, and it is not suitable for in vivo detection of degranulation. At the aim of real time imaging of mast cell degranulation at single cell level, we here developed a fluorescent protein-based indicator of degranulation, designated immuno-pHluorin (impH). When expressed in mast cells, impH is located in the membrane of secretory granules and non-fluorescent under homeostatic conditions while it turns fluorescent following degranulation, due to the pH change inside of granules during exocytosis. impH enabled us to detect polarized degranulation within one single cell when mast cells were stimulated via the small area of cell surface. Transplantation of impH-expressing mast cells into mast cell-deficient mice demonstrated that impH could function as a real-time indicator of degranulation in vivo. Thus, impH is a useful tool for imaging of mast cell activation and degranulation in vitro and in vivo, and may be applied for screening of reagents regulating mast cell degranulation. (C) 2016 Elsevier Inc. All rights reserved.

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