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Cerebral Cortex, Vol. 12, No. 5, 515-525, May 2002
© 2002 Oxford University Press

Similar Perisynaptic Glial Localization for the Na+,K+-ATPase {alpha}2 Subunit and the Glutamate Transporters GLAST and GLT-1 in the Rat Somatosensory Cortex

N. Cholet, L. Pellerin1, P. J. Magistretti1 and E. Hamel

Laboratory of Cerebrovascular Research, Montreal Neurological Institute, McGill University, 3801 University Street, Montréal, Québec, Canada, H3A 2B4 and , 1 Institut de Physiologie, Université de Lausanne, 7 rue du Bugnon, 1005 Lausanne, Switzerland

Professor Edith Hamel, Montreal Neurological Institute, 3801 University Street, Room 748, Montréal, QC, Canada H3A 2B4. Email: edith.hamel{at}mcgill.ca.

Several isoenzymes of the Na+,K+-ATPase are expressed in brain but their specific roles are poorly understood. Recently, it was suggested that an isoenzyme of the Na+,K+-ATPase containing the {alpha}2 subunit, together with the glutamate transporters GLAST and GLT-1, participate in a coupling mechanism between neuronal activity and energy metabolism taking place in astrocytes. To substantiate this hypothesis, we compared the distribution of {alpha}2, GLAST and/or GLT-1 in the rat cerebral cortex using double immunofluorescence and confocal microscopy, and immunocytochemistry at the electron microscopic level. We also investigated the relationship between {alpha}2, GLAST or GLT-1 and asymmetrical synaptic junctions (largely glutamatergic) and GABAergic nerve terminals. Results show that the {alpha}2 subunit has an exclusive astroglial localization, and that it is almost completely co-distributed with GLAST and GLT-1 when evaluated by confocal microscopy. This similar distribution was confirmed at the ultrastructural level, which further showed that the vast majority of the {alpha}2 staining (73% of all labelled elements), like that of GLAST and GLT-1, was located in glial leaflets surrounding dendritic spines and the dendritic and/or axonal elements of asymmetrical (glutamatergic) axo-dendritic synapses. Synapses ensheathed by {alpha}2, GLAST or GLT-1 virtually never included (<=2%) GABAergic nerve terminals or synaptic junctions. However, a subset of GABAergic nerve terminals (10–14%) were directly apposed to asymmetrical axo-dendritic junctions surrounded by {alpha}2, GLAST or GLT-1. Altogether these results demonstrate that {alpha}2, GLAST and GLT-1 have comparable perisynaptic distribution within cortical astrocytes most likely associated with glutamatergic synapses.


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