Literature DB >> 2446328

Tissue-specific expression of the RI and RII sodium channel subtypes.

D Gordon1, D Merrick, V Auld, R Dunn, A L Goldin, N Davidson, W A Catterall.   

Abstract

Anti-peptide antibodies that distinguish between the rat brain sodium channel subtypes referred to as RI and RII were prepared and used to determine their relative expression in nerve and muscle tissues. Sodium channels purified from rat brain are approximately 18% RI and 80% RII. In brain, the RII subtype is preferentially expressed with RI/RII ratios ranging from 0.07 in the hippocampus to 0.17 in the cerebral cortex. The RI subtype is preferentially expressed in more caudal areas of the central nervous system with values of RI/RII of 0.98 for medulla oblongata and 2.2 for spinal cord. Expression of additional unidentified sodium channel subtype(s) is detected in midbrain, medulla, and spinal cord, and expression of unidentified sodium channel subtypes predominates over expression of RI and RII in retina and optic nerve. The RI and RII subtypes are primarily expressed in the central nervous system and are not detected in significant numbers in skeletal or cardiac muscle, sympathetic ganglia, adrenal medulla, sciatic nerve, or cauda equina. The RII subtype appears first in development of both brain and spinal cord but declines in adult spinal cord as the RI subtype increases. The strict regional expression of these two sodium channel subtypes suggests that they may have distinct functional properties or physiological roles.

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Year:  1987        PMID: 2446328      PMCID: PMC299610          DOI: 10.1073/pnas.84.23.8682

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  23 in total

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2.  Muscle surface membranes: preparative methods affect apparent chemical properties and neurotoxin binding.

Authors:  R L Barchi; J B Weigele; D M Chalikian; L E Murphy
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3.  Partial purification and functional expression of brain mRNAs coding for neurotransmitter receptors and voltage-operated channels.

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4.  Molecular characteristics and functional reconstitution of muscle voltage-sensitive sodium channels.

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Review 5.  Voltage-regulated sodium channel molecules.

Authors:  W S Agnew
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6.  Appearance of [3H]saxitoxin binding sites in developing rat brain.

Authors:  J Baumgold; I Zimmerman; L Bambrick
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7.  A new method for labelling saxitoxin and its binding to non-myelinated fibres of the rabbit vagus, lobster walking leg, and garfish olfactory nerves.

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8.  Cyclic AMP-dependent phosphorylation of the alpha subunit of the sodium channel in synaptic nerve ending particles.

Authors:  M R Costa; W A Catterall
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Authors:  C J Waechter; J W Schmidt; W A Catterall
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10.  Existence of distinct sodium channel messenger RNAs in rat brain.

Authors:  M Noda; T Ikeda; T Kayano; H Suzuki; H Takeshima; M Kurasaki; H Takahashi; S Numa
Journal:  Nature       Date:  1986 Mar 13-19       Impact factor: 49.962

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  50 in total

1.  A scorpion alpha-like toxin that is active on insects and mammals reveals an unexpected specificity and distribution of sodium channel subtypes in rat brain neurons.

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3.  The glial voltage-gated sodium channel: cell- and tissue-specific mRNA expression.

Authors:  S Gautron; G Dos Santos; D Pinto-Henrique; A Koulakoff; F Gros; Y Berwald-Netter
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Review 4.  Tissue-specific expression of the voltage-sensitive sodium channel.

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Review 7.  Molecular mechanism of scorpion neurotoxins acting on sodium channels: insight into their diverse selectivity.

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8.  Regional and temporal expression of sodium channel messenger RNAs in the rat brain during development.

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9.  Temperature- and age-dependent seizures in a mouse model of severe myoclonic epilepsy in infancy.

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10.  Subunits of purified calcium channels: a 212-kDa form of alpha 1 and partial amino acid sequence of a phosphorylation site of an independent beta subunit.

Authors:  K S De Jongh; D K Merrick; W A Catterall
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