TY - JOUR
T1 - Real-time imaging of mast cell degranulation in vitro and in vivo
AU - Horiguchi, Kayo
AU - Yoshikawa, Soichiro
AU - Saito, Asuka
AU - Haddad, Salma
AU - Ohta, Takuya
AU - Miyake, Kensuke
AU - Yamanishi, Yoshinori
AU - Karasuyama, Hajime
N1 - Funding Information:
We thank Dr. Gero Miesenböck for providing the construct of pHluorin, Dr. S.J. Galli, Dr. S. Nakae, and Dr. K. Sudo for providing Kit W−sh/W−sh mice, and Dr. T. Takai for providing Fcer1g −/− mice. This work was supported by research Grants from JST , the Japanese Ministry of Education, Culture, Sports, Science and Technology [ 15H05786 ] (to H. Karasuyama), and grants from Urakami foundation for Food and Food Culture Promotion (to S. Yoshikawa) and Sasakawa foundation (to K. Horiguchi).
Publisher Copyright:
© 2016 Elsevier Inc.
PY - 2016/10/21
Y1 - 2016/10/21
N2 - 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 β-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.
AB - 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 β-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.
KW - Degranulation
KW - Exocytosis
KW - Imaging
KW - Mast cell
KW - VAMP-8
KW - pH sensor
UR - http://www.scopus.com/inward/record.url?scp=84989852769&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84989852769&partnerID=8YFLogxK
U2 - 10.1016/j.bbrc.2016.09.100
DO - 10.1016/j.bbrc.2016.09.100
M3 - Article
C2 - 27664704
AN - SCOPUS:84989852769
SN - 0006-291X
VL - 479
SP - 517
EP - 522
JO - Biochemical and Biophysical Research Communications
JF - Biochemical and Biophysical Research Communications
IS - 3
ER -