Literature DB >> 10696142

Ion channel expression by astrocytes in situ: comparison of different CNS regions.

A Bordey1, H Sontheimer.   

Abstract

Patch-clamp recordings were obtained in brain slices from 283 rat astrocytes. The expression of voltage-activated whole-cell currents was compared in four different CNS regions (hippocampus, cerebral cortex, spinal cord, and cerebellum). Our data show that CNS astrocytes do not show significant regional differences in their ion channel complement. With the exception of cerebellar Bergmann glial cells, essentially all astrocytes express a combination of delayed rectifying outward K(+) currents, transient A-type K(+) currents, and small Na(+) currents. Developmentally, an increasing percentage of astrocytes and Bergmann glial cells express inwardly rectifying K(+) currents. We did not observe cells that were passive, i.e., lacking voltage-activated currents. A few cells that appeared "passive" in initial recordings showed voltage-activated K(+) currents after off-line leak subtraction. The heterogeneity observed in the ion channel complement was found to be identical when cell-to-cell variations observed within a given CNS region and between various CNS regions were compared, suggesting a common and fairly stereotypical complement of ion channels in CNS astrocytes. Ion channel expression in Bergmann glial cells differed from that of all other CNS regions studied. These cells typically showed very low input resistances attributable to a significant time- and voltage-independent resting K(+) conductance. However, as with electrophysiologically "passive"-appearing astrocytes, Bergmann glial cells showed expression of delayed rectifying K(+) currents after off-line leak subtraction. Inwardly rectifying K(+) currents were observed in Bergmann glial cells after postnatal day 17. Collectively, our data suggest that all astrocytes contain voltage-gated ion channels that display a common pattern of expression during development. Copyright 2000 Wiley-Liss, Inc.

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Year:  2000        PMID: 10696142     DOI: 10.1002/(sici)1098-1136(200003)30:1<27::aid-glia4>3.0.co;2-#

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


  28 in total

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2.  Electrophysiological classification of P2X7 receptors in rat cultured neocortical astroglia.

Authors:  W Nörenberg; J Schunk; W Fischer; H Sobottka; T Riedel; J F Oliveira; H Franke; P Illes
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3.  Nonsynaptic GABA signaling in postnatal subventricular zone controls proliferation of GFAP-expressing progenitors.

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4.  Functional expression of Kir4.1 channels in spinal cord astrocytes.

Authors:  M L Olsen; H Higashimori; S L Campbell; J J Hablitz; H Sontheimer
Journal:  Glia       Date:  2006-04-01       Impact factor: 7.452

5.  High extracellular K(+) evokes changes in voltage-dependent K(+) and Na (+) currents and volume regulation in astrocytes.

Authors:  Helena Neprasova; Miroslava Anderova; David Petrik; Lydia Vargova; Sarka Kubinova; Alexandr Chvatal; Eva Sykova
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6.  Altered functional properties of satellite glial cells in compressed spinal ganglia.

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Review 7.  The astrocyte odyssey.

Authors:  Doris D Wang; Angélique Bordey
Journal:  Prog Neurobiol       Date:  2008-10-01       Impact factor: 11.685

8.  Astrocytic glutamate uptake is slow and does not limit neuronal NMDA receptor activation in the neonatal neocortex.

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Journal:  Glia       Date:  2015-04-27       Impact factor: 7.452

9.  Bergmann glial GlyT1 mediates glycine uptake and release in mouse cerebellar slices.

Authors:  Hao Huang; Latifa Barakat; Doris Wang; Angélique Bordey
Journal:  J Physiol       Date:  2004-08-26       Impact factor: 5.182

10.  Novel role of the nociceptin system as a regulator of glutamate transporter expression in developing astrocytes.

Authors:  Logan C Meyer; Caitlin E Paisley; Esraa Mohamed; John W Bigbee; Tomasz Kordula; Hope Richard; Kabirullah Lutfy; Carmen Sato-Bigbee
Journal:  Glia       Date:  2017-09-14       Impact factor: 7.452

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