TY - CHAP
T1 - Update on Eosinophil Interaction with Mast Cells
T2 - The Allergic Effector Unit
AU - Gangwar, Roopesh Singh
AU - Pahima, Hadas
AU - Puzzovio, Pier Giorgio
AU - Levi-Schaffer, Francesca
N1 - Funding Information: This work was supported by the Israel Science Foundation and Aimwell Charitable Trust (London, UK). F. Levi-Schaffer is affiliated with the Dr. Adolph and Klara Brettler Center for Research in Molecular Pharmacology and Therapeutics, School of Pharmacy of the Hebrew University of Jerusalem. Publisher Copyright: © 2021, Springer Science+Business Media, LLC, part of Springer Nature.
PY - 2021
Y1 - 2021
N2 - Mast cells and eosinophils are the key effector cells of allergy [1]. In general, allergic reactions are composed of two phases, namely an early phase and a late phase, and after that resolution occurs. If the allergic reactions fail to resolve after the late phase, allergic inflammation (AI) can evolve into a chronic phase mainly involving mast cells and eosinophils that abundantly coexist in the inflamed tissue in the late and chronic phases and cross-talk in a bidirectional manner. We defined these bidirectional interactions between MCs and Eos, as the “allergic effector unit.” This cross talk is mediated by both physical cell-cell contacts through cell surface receptors such as CD48, 2B4, and respective ligands and through released mediators such as various specific granular mediators, arachidonic acid metabolites, cytokines, and chemokines [2, 3]. The allergic effector unit can be studied in vitro in a customized co-culture system using mast cells and eosinophils derived from either mouse or human sources.
AB - Mast cells and eosinophils are the key effector cells of allergy [1]. In general, allergic reactions are composed of two phases, namely an early phase and a late phase, and after that resolution occurs. If the allergic reactions fail to resolve after the late phase, allergic inflammation (AI) can evolve into a chronic phase mainly involving mast cells and eosinophils that abundantly coexist in the inflamed tissue in the late and chronic phases and cross-talk in a bidirectional manner. We defined these bidirectional interactions between MCs and Eos, as the “allergic effector unit.” This cross talk is mediated by both physical cell-cell contacts through cell surface receptors such as CD48, 2B4, and respective ligands and through released mediators such as various specific granular mediators, arachidonic acid metabolites, cytokines, and chemokines [2, 3]. The allergic effector unit can be studied in vitro in a customized co-culture system using mast cells and eosinophils derived from either mouse or human sources.
KW - Allergic effector unit
KW - BMEos
KW - BMMCs
KW - Co-culture
KW - Mast cell-eosinophil interactions
KW - Murine AEU
UR - http://www.scopus.com/inward/record.url?scp=85100362411&partnerID=8YFLogxK
U2 - https://doi.org/10.1007/978-1-0716-1095-4_18
DO - https://doi.org/10.1007/978-1-0716-1095-4_18
M3 - Chapter
C2 - 33486740
T3 - Methods in Molecular Biology
SP - 221
EP - 242
BT - Methods in Molecular Biology
ER -