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Neurohypophyseal Hormones: From Genomics and Physiology to Disease
1Laboratory of Neurophysiology, 2Division of Molecular Neurobiology, and 3Laboratory of Morphodiversity, National Institute for Basic Biology, Okazaki, Aichi; 4School of Life Science, The Graduate University for Advanced Studies, Okazaki, Aichi; 5Department of Applied Biology, Kyoto Institute for Technology, Matsugasaki, Sakyo, Kyoto; 6Department of Genetic and Behavioral Neuroscience, Graduate School of Medicine, Gunma University, Maebashi, Gunma; and 7The Institute of Physical and Chemical Research, Brain Science Institute, Wako, Saitama, Japan
Submitted 25 August 2005 ; accepted in final form 11 October 2005
Nax is an atypical sodium channel that is assumed to be a descendant of the voltage-gated sodium channel family. Our recent studies on the Nax-gene-targeting mouse revealed that Nax channel is localized to the circumventricular organs (CVOs), the central loci for the salt and water homeostasis in mammals, where the Nax channel serves as a sodium-level sensor of the body fluid. To understand the cellular mechanism by which the information sensed by Nax channels is transferred to the activity of the organs, we dissected the subcellular localization of Nax in the present study. Double-immunostaining and immunoelectron microscopic analyses revealed that Nax is exclusively localized to perineuronal lamellate processes extended from ependymal cells and astrocytes in the organs. In addition, glial cells isolated from the subfornical organ, one of the CVOs, were sensitive to an increase in the extracellular sodium level, as analyzed by an ion-imaging method. These results suggest that glial cells bearing the Nax channel are the first to sense a physiological increase in the level of sodium in the body fluid, and they regulate the neural activity of the CVOs by enveloping neurons. Close communication between inexcitable glial cells and excitable neural cells thus appears to be the basis of the central control of the salt homeostasis.
sodium sensor; salt homeostasis; glial sodium channel; Nav2; astrocyte; ependymal cell; GABAergic neuron; neuron-glia interaction
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