Norepinephrine induces rapid and long-lasting phosphorylation and redistribution of connexin 43 in cortical astrocytes
Creators
- 1. Graduate School of Environment and Information Sciences, Yokohama National University (Japan)
- 2. Precursory Research for Embryonic Science and Technology (PRESTO), Japan Science and Technology Agency (JST), Kawaguchi, Saitama, 332-0012 (Japan)
- 3. Department of Pharmacology, School of Medicine, Keio University, Shinanomachi, Shinjuku, 160-8582 (Japan)
- 4. College of Engineering, Yokohama National University, Kanagawa, 240-8501 (Japan)
Description
Highlights: • Norepinephrine (NE) induces phosphorylation of connexin 43 (Cx43) in the brain. • This phosphorylation occurs within minutes and lasts for tens of minutes. • NE acts directly on astrocytes to induce phosphorylation of Cx43 via PKC pathway. • Phosphorylation of Cx43 induces its redistribution out from the gap junction plaque. • These data suggest biochemical gliomodulatory action of NE in the cerebral cortex. Norepinephrine (NE) modulates brain functions depending on both the internal and external environment. While the neuromodulatory actions of NE have been well characterized, the response and involvement of cortical astrocytes to physiological noradrenergic systems remain largely unknown, especially at the molecular level. In this study, we biochemically characterize the action of NE on astrocytes of the murine neocortex. NE stimulation of acute brain slices rapidly increase phosphorylation of connexin 43 (Cx43) at Serine (Ser) 368, in slices from both juvenile and adolescent animals. The phosphorylation is mediated by the protein kinase C (PKC) pathway under the α1-adrenergic receptor and remains elevated for tens of minutes following brief exposure to NE, well after the intracellular calcium level returns to normal level, suggesting the plastic nature of this phosphorylation event. Importantly, this phosphorylation event persists in the absence of neuronal transmissions, suggesting that the effect of NE on Cx43 phosphorylation is induced directly on astrocytes. Furthermore, these NE-induced phosphorylations are associated with biochemical dissociation of Cx43 from gap-junctional plaques to non-junctional compartments. Finally, we show that pharmacological manipulation of the noradrenergic system using psychoactive drugs modulates phosphorylation of Cx43 in the cerebral cortex in vivo. These data suggest that NE acts directly on astrocytes in parallel with neurons and modulates functionally critical connexin channel proteins in a plastic manner. Thus, plasticity of astrocytes induced by the "gliomodulatory" actions of NE may play important roles in their physiological as well as pharmacological actions in the brain.
Availability note (English)
Available from http://dx.doi.org/10.1016/j.bbrc.2018.09.021Additional details
Identifiers
- DOI
- 10.1016/j.bbrc.2018.09.021;
- PII
- S0006291X18319375;
Publishing Information
- Journal Title
- Biochemical and Biophysical Research Communications
- Journal Volume
- 504
- Journal Issue
- 4
- Journal Page Range
- p. 690-697
- ISSN
- 0006-291X
- CODEN
- BBRCA9
INIS
- Country of Publication
- United States
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 53024378
- Subject category
- S60: APPLIED LIFE SCIENCES;
- Descriptors DEI
- CALCIUM; CEREBRAL CORTEX; NERVE CELLS; NORADRENALINE; PHOSPHOTRANSFERASES; RECEPTORS; SERINE
- Descriptors DEC
- ADRENAL HORMONES; ALKALINE EARTH METALS; AMINO ACIDS; ANIMAL CELLS; AUTONOMIC NERVOUS SYSTEM AGENTS; BODY; BRAIN; CARBOXYLIC ACIDS; CARDIOTONICS; CARDIOVASCULAR AGENTS; CENTRAL NERVOUS SYSTEM; CEREBRUM; DRUGS; ELEMENTS; ENZYMES; HORMONES; HYDROXY ACIDS; MEMBRANE PROTEINS; METALS; NERVOUS SYSTEM; NEUROREGULATORS; ORGANIC ACIDS; ORGANIC COMPOUNDS; ORGANS; PHOSPHORUS-GROUP TRANSFERASES; PROTEINS; SOMATIC CELLS; SYMPATHOMIMETICS; TRANSFERASES
Optional Information
- Copyright
- Copyright (c) 2018 Elsevier Inc. All rights reserved.