Key result
NCX1-3 isoforms are widely expressed in cortical and hippocampal astrocytes, including mitochondria and perivascular endfeet.
All three NCX isoforms are widely expressed in astrocytes, suggesting they play a role in maintaining calcium homeostasis in glial cells and regulating blood-brain barrier function.
Na+/Ca2+ (NCX1, 2 and 3) play relevant role in neural cells, where variations of cytosolic Ca2+ represent pivotal event in many physiological and pathological processes. Astrocytes display a type of excitability based on changes in Ca2+. the present study, electron microscopic immunohistochemistry was applied to investigate the expression of the three NCX1-3 isoforms, in astrocytes of cerebral cortex and hippocampus. Results showed that a conspicuous population of astrocytic expressed NCX1–3 in both brain areas. Immunolabeling for NCX1-3 was observed in many glial profiles of various size, in distal astrocytic processes in contiguity of synaptic structures, suggesting the involvement of NCX in shaping astrocytic [Ca]i transients evoked by adjacent synaptic activity. NCX1-3 immunoreactivities (irs) were expressed in astrocytic mitochondria, indicating an important contribution to mitochondrial Ca2+ in this cell type in situ. In addition, all NCX isoforms were consistently expressed in perivascular astrocytic endfeet, suggesting an important role in regulating the barrier function of blood-brain barrier (BBB). Present immunomorphological work showed that in both brain regions all NCX isoforms were in astrocytes, thus pointing to a widespread role of the three exchangers in maintaining Ca2+ in glial cells suggesting that distinct NCX isoforms may share analogous physiological roles in the brain in vivo.
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Salucci et al. (2009) studied this question. Electron microscopic immunohistochemistry was evaluated on Expression of NCX1-3 protein isoforms in astrocytes of cerebral cortex and hippocampus. Electron microscopic immunohistochemistry showed that NCX1-3 isoforms are widely expressed in astrocytes of the cerebral cortex and hippocampus, including in mitochondria and perivascular endfeet.
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