Literature DB >> 2452594

Modulation of ion channels in neurons and other cells.

I B Levitan1.   

Abstract

The field of ion channel modulation has entered a stage of maturity. The development of powerful new molecular biological and biophysical approaches has provided important new insights into the structure and function of ion channels and has revealed them as dynamic entities whose activity can be regulated. The physiological consequences of such regulation are obvious for so-called excitable cells like nerve and muscle cells, but it is also evident that modulation occurs in many other cell types, where its effects on the lifestyle of the cell are less clear. Furthermore, the number of ion channels that have been shown to be subject to modulation continues to increase, and the end is not yet in sight. For example, exciting information is beginning to emerge about gating and conduction properties of the large class of channels coupled to excitatory amino acid receptors (Mayer 1987), but their modulation has not yet been studied in any detail. In any event, there no longer is any doubt that modulatability is an intrinsic property of many and perhaps all membrane ion channels. The mechanisms of channel modulation are also turning out to be more diverse than was first suspected. One possible explanation for this diversity is to provide a broad temporal spectrum for the regulation of channel activity. One temporal extreme may be a directly coupled system such as the nicotinic acetylcholine receptor/channel, where interactions between the several subunits of a single macromolecular complex determine rapid channel gating. The other extreme may be covalent modification (by protein phosphorylation or other covalent change), which results in a functional change that can long outlast the initial stimulus. G-protein modulation, which involves the (presumably) noncovalent interaction between distinct membrane proteins, may provide for intermediate duration changes in channel properties. Whether these mechanisms will be joined by others that provide for an even more subtle temporal discrimination is an exciting question for the future.

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Year:  1988        PMID: 2452594     DOI: 10.1146/annurev.ne.11.030188.001003

Source DB:  PubMed          Journal:  Annu Rev Neurosci        ISSN: 0147-006X            Impact factor:   12.449


  42 in total

1.  Modulation of Kv3 potassium channels expressed in CHO cells by a nitric oxide-activated phosphatase.

Authors:  H Moreno; E Vega-Saenz de Miera; M S Nadal; Y Amarillo; B Rudy
Journal:  J Physiol       Date:  2001-02-01       Impact factor: 5.182

2.  Modulators with convergent cellular actions elicit distinct circuit outputs.

Authors:  A M Swensen; E Marder
Journal:  J Neurosci       Date:  2001-06-01       Impact factor: 6.167

3.  Molecular cloning and expression of a Kv1.1-like potassium channel from the electric organ of Electrophorus electricus.

Authors:  W B Thornhill; I Watanabe; J J Sutachan; M B Wu; X Wu; J Zhu; E Recio-Pinto
Journal:  J Membr Biol       Date:  2003-11-01       Impact factor: 1.843

4.  Phosphorylation modulates the voltage dependence of channels reconstituted from the major intrinsic protein of lens fiber membranes.

Authors:  G R Ehring; N Lagos; G A Zampighi; J E Hall
Journal:  J Membr Biol       Date:  1992-02       Impact factor: 1.843

5.  Genetic analysis of the Shaker gene complex of Drosophila melanogaster.

Authors:  A Ferrús; S Llamazares; J L de la Pompa; M A Tanouye; O Pongs
Journal:  Genetics       Date:  1990-06       Impact factor: 4.562

6.  Cloning of components of a novel subthreshold-activating K(+) channel with a unique pattern of expression in the cerebral cortex.

Authors:  M J Saganich; E Vega-Saenz de Miera; M S Nadal; H Baker; W A Coetzee; B Rudy
Journal:  J Neurosci       Date:  1999-12-15       Impact factor: 6.167

7.  Different G proteins mediate the opioid inhibition or enhancement of evoked [5-methionine]enkephalin release.

Authors:  A R Gintzler; H Xu
Journal:  Proc Natl Acad Sci U S A       Date:  1991-06-01       Impact factor: 11.205

8.  L-type Ca2+ channels in inspiratory neurones of mice and their modulation by hypoxia.

Authors:  S L Mironov; D W Richter
Journal:  J Physiol       Date:  1998-10-01       Impact factor: 5.182

9.  omega-Grammotoxin blocks action-potential-induced Ca2+ influx and whole-cell Ca2+ current in rat dorsal-root ganglion neurons.

Authors:  T M Piser; R A Lampe; R A Keith; S A Thayer
Journal:  Pflugers Arch       Date:  1994-02       Impact factor: 3.657

10.  The ATP and Mg2+ dependence of Na(+)-K(+)-2Cl- cotransport reflects a requirement for protein phosphorylation: studies using calyculin A.

Authors:  H C Palfrey; E B Pewitt
Journal:  Pflugers Arch       Date:  1993-11       Impact factor: 3.657

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