Zinc is a novel intracellular second messenger

Author:

Yamasaki Satoru1,Sakata-Sogawa Kumiko2,Hasegawa Aiko13,Suzuki Tomoyuki1,Kabu Koki13,Sato Emi13,Kurosaki Tomohiro4,Yamashita Susumu3,Tokunaga Makio256,Nishida Keigo13,Hirano Toshio13

Affiliation:

1. Laboratory for Cytokine Signaling,

2. Research Unit for Single Molecule Immunoimaging, and

3. Laboratory of Developmental Immunology, Graduate School of Frontier Biosciences and Graduate School of Medicine, Osaka University, Osaka 565-0871, Japan

4. Laboratory for Lymphocyte Differentiation, RIKEN Research Center for Allergy and Immunology, Yokohama, Kanagawa 230-0045, Japan

5. Structural Biology Center, National Institute of Genetics, and

6. Department of Genetics, The Graduate University for Advanced Studies, Shizuoka 411-8540, Japan

Abstract

Zinc is an essential trace element required for enzymatic activity and for maintaining the conformation of many transcription factors; thus, zinc homeostasis is tightly regulated. Although zinc affects several signaling molecules and may act as a neurotransmitter, it remains unknown whether zinc acts as an intracellular second messenger capable of transducing extracellular stimuli into intracellular signaling events. In this study, we report that the cross-linking of the high affinity immunoglobin E receptor (Fcε receptor I [FcεRI]) induced a release of free zinc from the perinuclear area, including the endoplasmic reticulum in mast cells, a phenomenon we call the zinc wave. The zinc wave was dependent on calcium influx and mitogen-activated protein kinase/extracellular signal-regulated kinase kinase activation. The results suggest that the zinc wave is involved in intracellular signaling events, at least in part by modulating the duration and strength of FcεRI-mediated signaling. Collectively, our findings indicate that zinc is a novel intracellular second messenger.

Publisher

Rockefeller University Press

Subject

Cell Biology

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