The Basoph8 Mice Enable an Unbiased Detection and a Conditional Depletion of Basophils
Basophils are granulocytes involved in parasite immunity and allergic diseases, known for their potent secretion of type 2 cytokines. Identifying their functions has proven to be controversial due to their relative rarity and their complex lineage phenotype. Here, we show that the expression of baso...
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2019-09-01
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doaj-4f9755fc5097464a9ad630d364947b4c2020-11-24T21:50:46ZengFrontiers Media S.A.Frontiers in Immunology1664-32242019-09-011010.3389/fimmu.2019.02143474564The Basoph8 Mice Enable an Unbiased Detection and a Conditional Depletion of BasophilsChristophe PellefiguesPalak MehtaMelanie Sarah ProutKarmella NaidooBibek YumnamJodie ChandlerSally ChappellKara FilbeyMali CamberisGraham Le GrosBasophils are granulocytes involved in parasite immunity and allergic diseases, known for their potent secretion of type 2 cytokines. Identifying their functions has proven to be controversial due to their relative rarity and their complex lineage phenotype. Here, we show that the expression of basophils lineage markers CD200R3 and FcεRIα is highly variable in inflammatory settings and hinders basophils identification by flow cytometry across multiple disease states or tissues. Fluorophore-conjugated antibody staining of these lineage markers strongly activates basophil type 2 cytokine expression, and represents a potential bias for coculture or in vivo transfer experiments. The Basoph8 is a mouse model where basophils specifically express a strong fluorescent reporter and the Cre recombinase. Basophils can be identified and FACS sorted unambiguously by their expression of the enhanced yellow fluorescent protein (eYFP) in these mice. We show that the expression of the eYFP is robust in vivo during inflammation, and in vitro on living basophils for at least 72 h, including during the induction of anaphylactoid degranulation. We bred and characterized the Basoph8xiDTR mice, in which basophils specifically express eYFP and the simian diphtheria toxin receptor (DTR). This model enables basophils conditional depletion relatively specifically ex vivo and in vivo during allergic inflammation and their detection as eYFP+ cells. In conclusion, we report underappreciated benefits of the commercially available Basoph8 mice to study basophils function.https://www.frontiersin.org/article/10.3389/fimmu.2019.02143/fullbasophilBasoph8depletionflow cytometryphenotype |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Christophe Pellefigues Palak Mehta Melanie Sarah Prout Karmella Naidoo Bibek Yumnam Jodie Chandler Sally Chappell Kara Filbey Mali Camberis Graham Le Gros |
spellingShingle |
Christophe Pellefigues Palak Mehta Melanie Sarah Prout Karmella Naidoo Bibek Yumnam Jodie Chandler Sally Chappell Kara Filbey Mali Camberis Graham Le Gros The Basoph8 Mice Enable an Unbiased Detection and a Conditional Depletion of Basophils Frontiers in Immunology basophil Basoph8 depletion flow cytometry phenotype |
author_facet |
Christophe Pellefigues Palak Mehta Melanie Sarah Prout Karmella Naidoo Bibek Yumnam Jodie Chandler Sally Chappell Kara Filbey Mali Camberis Graham Le Gros |
author_sort |
Christophe Pellefigues |
title |
The Basoph8 Mice Enable an Unbiased Detection and a Conditional Depletion of Basophils |
title_short |
The Basoph8 Mice Enable an Unbiased Detection and a Conditional Depletion of Basophils |
title_full |
The Basoph8 Mice Enable an Unbiased Detection and a Conditional Depletion of Basophils |
title_fullStr |
The Basoph8 Mice Enable an Unbiased Detection and a Conditional Depletion of Basophils |
title_full_unstemmed |
The Basoph8 Mice Enable an Unbiased Detection and a Conditional Depletion of Basophils |
title_sort |
basoph8 mice enable an unbiased detection and a conditional depletion of basophils |
publisher |
Frontiers Media S.A. |
series |
Frontiers in Immunology |
issn |
1664-3224 |
publishDate |
2019-09-01 |
description |
Basophils are granulocytes involved in parasite immunity and allergic diseases, known for their potent secretion of type 2 cytokines. Identifying their functions has proven to be controversial due to their relative rarity and their complex lineage phenotype. Here, we show that the expression of basophils lineage markers CD200R3 and FcεRIα is highly variable in inflammatory settings and hinders basophils identification by flow cytometry across multiple disease states or tissues. Fluorophore-conjugated antibody staining of these lineage markers strongly activates basophil type 2 cytokine expression, and represents a potential bias for coculture or in vivo transfer experiments. The Basoph8 is a mouse model where basophils specifically express a strong fluorescent reporter and the Cre recombinase. Basophils can be identified and FACS sorted unambiguously by their expression of the enhanced yellow fluorescent protein (eYFP) in these mice. We show that the expression of the eYFP is robust in vivo during inflammation, and in vitro on living basophils for at least 72 h, including during the induction of anaphylactoid degranulation. We bred and characterized the Basoph8xiDTR mice, in which basophils specifically express eYFP and the simian diphtheria toxin receptor (DTR). This model enables basophils conditional depletion relatively specifically ex vivo and in vivo during allergic inflammation and their detection as eYFP+ cells. In conclusion, we report underappreciated benefits of the commercially available Basoph8 mice to study basophils function. |
topic |
basophil Basoph8 depletion flow cytometry phenotype |
url |
https://www.frontiersin.org/article/10.3389/fimmu.2019.02143/full |
work_keys_str_mv |
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