Calcium transients trigger switch-like discharge of prostaglandin E2 in an extracellular signal-regulated kinase-dependent manner

Author:

Watabe Tetsuya12,Yamahira Shinya1,Takakura Kanako1,Thumkeo Dean3,Narumiya Shuh3,Matsuda Michiyuki124ORCID,Terai Kenta2ORCID

Affiliation:

1. Research Center for Dynamic Living Systems, Graduate School of Biostudies, Kyoto University

2. Department of Pathology and Biology of Diseases, Graduate School of Medicine, Kyoto University

3. Department of Drug Discovery Medicine, Graduate School of Medicine, Kyoto University

4. Institute for Integrated Cell-Material Sciences, Kyoto University

Abstract

Prostaglandin E2 (PGE2) is a key player in a plethora of physiological and pathological events. Nevertheless, little is known about the dynamics of PGE2 secretion from a single cell and its effect on the neighboring cells. Here, by observing confluent Madin–Darby canine kidney (MDCK) epithelial cells expressing fluorescent biosensors, we demonstrate that calcium transients in a single cell cause PGE2-mediated radial spread of PKA activation (RSPA) in neighboring cells. By in vivo imaging, RSPA was also observed in the basal layer of the mouse epidermis. Experiments with an optogenetic tool revealed a switch-like PGE2 discharge in response to the increasing cytoplasmic Ca2+ concentrations. The cell density of MDCK cells correlated with the frequencies of calcium transients and the following RSPA. The extracellular signal-regulated kinase (ERK) activation also enhanced the frequency of RSPA in MDCK and in vivo. Thus, the PGE2 discharge is regulated temporally by calcium transients and ERK activity.

Funder

Japan Society for the Promotion of Science

Core Research for Evolutional Science and Technology

Moonshot Research and Development Program

Fugaku Foundation

Princess Takamatsu Cancer Research Fund

Publisher

eLife Sciences Publications, Ltd

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

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