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Mast cell maturation is driven via a group III phospholipase A2-prostaglandin D2–DP1 receptor paracrine axis

Authors :
Masataka Nakamura
Makoto Arita
Masanori Nakamura
Naotomo Kambe
Satoshi Nakamizo
Remi Murase
Hiroyuki Hirai
Kikuko Watanabe
Michael H. Gelb
Momoko Kawana
Yukihiko Sugimoto
Yasumasa Nishito
Kazutaka Ikeda
Yoshitaka Taketomi
Kazushi Morimoto
Ryo Taguchi
Kei Yamamoto
Noriko Ueno
Kosuke Aritake
Satoshi Tanaka
Takehiko Yokomizo
Mariko Sakanaka
Yoshihiro Urade
Kenji Kabashima
Shuh Narumiya
Makoto Murakami
Takao Shimizu
Motonao Nakamura
Hiroyasu Sato
Shuntaro Hara
Chisei Ra
Takumi Kojima
Yoshimichi Okayama
Source :
Nature Immunology. 14:554-563
Publication Year :
2013
Publisher :
Springer Science and Business Media LLC, 2013.

Abstract

Microenvironment-based alterations in phenotypes of mast cells influence the susceptibility to anaphylaxis, yet the mechanisms underlying proper maturation of mast cells toward an anaphylaxis-sensitive phenotype are incompletely understood. Here we report that PLA2G3, a mammalian homolog of anaphylactic bee venom phospholipase A2, regulates this process. PLA2G3 secreted from mast cells is coupled with fibroblastic lipocalin-type PGD2 synthase (L-PGDS) to provide PGD2, which facilitates mast-cell maturation via PGD2 receptor DP1. Mice lacking PLA2G3, L-PGDS or DP1, mast cell–deficient mice reconstituted with PLA2G3-null or DP1-null mast cells, or mast cells cultured with L-PGDS–ablated fibroblasts exhibited impaired maturation and anaphylaxis of mast cells. Thus, we describe a lipid-driven PLA2G3–L-PGDS–DP1 loop that drives mast cell maturation.

Details

ISSN :
15292916 and 15292908
Volume :
14
Database :
OpenAIRE
Journal :
Nature Immunology
Accession number :
edsair.doi.dedup.....9ec611c3f3c569530f3ccfa18c7d3e43
Full Text :
https://doi.org/10.1038/ni.2586