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Analyzing the Functions of Mast Cells In Vivo Using 'Mast Cell Knock-in' Mice
Published on: May 27, 2015
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New inducible mast cell-deficient mouse model (Mcpt5/Cma1DTR)
Hayato Sasaki1, Madoka Imanishi1, Daisuke Fujikura1
1School of Veterinary Medicine, Kitasato University, Towada, 034-8628, Japan.
Biochemical and Biophysical Research Communications
|March 16, 2021
Summary
New mast cell-deficient mice (Mcpt5/Cma1DTR) enable targeted depletion of all mast cell populations. This model is crucial for in vivo research into mast cell functions and roles in various biological processes.
Area of Science:
- Immunology
- Genetics
Background:
- Mast cells play vital roles in vivo, necessitating models for their study.
- Existing mouse models do not achieve specific depletion of all mast cell populations.
Purpose of the Study:
- To develop a novel mouse model for conditional depletion of all mast cell populations.
- To validate the efficacy of this model in eliminating mast cells across various tissues.
Main Methods:
- Generation of knock-in mice (Mcpt5/Cma1DTR) expressing the diphtheria toxin receptor under the Mcpt5 promoter.
- Intraperitoneal administration of diphtheria toxin (DT) to induce mast cell depletion.
- Flow cytometry, histological analysis, and passive cutaneous anaphylaxis assays to assess mast cell reduction and specificity.
Main Results:
- DT treatment in Mcpt5/Cma1DTR/+ mice achieved near-complete mast cell depletion (97.7%-100%) in multiple tissues.
- Passive cutaneous anaphylaxis confirmed mast cell deficiency in the ear.
- Minimal impact on other cell types, with only a small percentage of marginal zone B cells affected.
Conclusions:
- The Mcpt5/Cma1DTR/+ mouse model allows for the conditional and near-complete depletion of all mast cell populations.
- This model is a valuable tool for in vivo research on mast cell functions without significant off-target effects.

