Kit-independent mast cell adhesion mediated by Notch

Author:

Murata Akihiko1,Hikosaka Mari2,Yoshino Miya1,Zhou Lan3,Hayashi Shin-Ichi1

Affiliation:

1. Division of Immunology, Department of Molecular and Cellular Biology, School of Life Science, Faculty of Medicine, Tottori University, Yonago, Tottori, Japan

2. Department of Stem Cell and Developmental Biology, Mie University Graduate School of Medicine, Tsu, Mie, Japan

3. Department of Pathology, Case Western Reserve University, Cleveland, OH, USA

Abstract

Abstract Kit/CD117 plays a crucial role in the cell–cell and cell–matrix adhesion of mammalian mast cells (MCs); however, it is unclear whether other adhesion molecule(s) perform important roles in the adhesion of MCs. In the present study, we show a novel Kit-independent adhesion mechanism of mouse cultured MCs mediated by Notch family members. On stromal cells transduced with each Notch ligand gene, Kit and its signaling become dispensable for the entire adhesion process of MCs from tethering to spreading. The Notch-mediated spreading of adherent MCs involves the activation of signaling via phosphatidylinositol 3-kinases and mitogen-activated protein kinases, similar to Kit-mediated spreading. Despite the activation of the same signaling pathways, while Kit supports the adhesion and survival of MCs, Notch only supports adhesion. Thus, Notch family members are specialized adhesion molecules for MCs that effectively replace the adhesion function of Kit in order to support the interaction of MCs with the surrounding cellular microenvironments.

Funder

Japan Society for the Promotion of Science

Takeda Science Foundation

Publisher

Oxford University Press (OUP)

Subject

Immunology,General Medicine,Immunology and Allergy

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