Literature DB >> 12237839

Chloride/anion channels in glial cell membranes.

Wolfgang Walz1.   

Abstract

At least seven different chloride/anion currents have now been identified in astrocytes, oligodendrocytes/Schwann cells, and microglia. Only for two of these currents is the corresponding gene known. One of these genes is not encoding for a chloride channel, but for a class of mitochondria-like pores also found in cell membranes. Astrocytes and oligodendrocytes differ in their resting properties: astrocytes accumulate chloride but do not have a significant permeability. Oligodendrocytes have a close to passive distribution and a significant permeability. Under certain circumstances, astrocytes can express a resting chloride conductance. Reactive and neoplastic astrocytes as well as astrocytes with an altered shape exhibit a resting conductance. The function of these channels certainly involves volume regulation. Other possible functions are potassium homeostasis, migration, proliferation (in microglia), and involvement in spreading depression waves. Of greatest interest are two phenomena discovered in situ: The ClC-2 channel is only found in astrocytic endfeet near blood capillaries adjacent to neuronal GABA(A) receptors. In the supraoptic nucleus of the hypothalamus, there is an osmosensitive astrocytic taurine release. This released taurine interacts with glycine receptors in neighboring neurons, causing inhibition. It is assumed that with the future availability of more in situ, rather than in vitro, studies, an increased number of such complex interactions between glial cells, neurons, and blood vessels will be discovered. Copyright 2002 Wiley-Liss, Inc.

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Year:  2002        PMID: 12237839     DOI: 10.1002/glia.10125

Source DB:  PubMed          Journal:  Glia        ISSN: 0894-1491            Impact factor:   7.452


  27 in total

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7.  Relative contribution of chloride channels and transporters to regulatory volume decrease in human glioma cells.

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Review 8.  Electrophysiological properties of NG2(+) cells: Matching physiological studies with gene expression profiles.

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9.  Role of Kir4.1 channels in growth control of glia.

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10.  Leukoencephalopathy upon disruption of the chloride channel ClC-2.

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