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rdf:type |
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lifeskim:mentions |
umls-concept:C0003320,
umls-concept:C0030685,
umls-concept:C0284555,
umls-concept:C0391871,
umls-concept:C0439799,
umls-concept:C0443146,
umls-concept:C0596235,
umls-concept:C0680255,
umls-concept:C0870432,
umls-concept:C1283071,
umls-concept:C1419778,
umls-concept:C1555465,
umls-concept:C1705417,
umls-concept:C1963578,
umls-concept:C2348205
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pubmed:issue |
6
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pubmed:dateCreated |
1999-8-2
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pubmed:abstractText |
Ryanodine receptors are a family of intracellular Ca2+ release channel proteins, which exist as tetrameric complexes of large ( approximately 5000 amino acid residue) polypeptide monomers. As well as controlling striated muscle contraction and neurotransmitter release, these channel proteins have been implicated in several pathological states. In order to characterise ryanodine receptors in various tissues, mouse monoclonal antibodies were developed against the type 1 isoform isolated from skeletal muscle. Several of these antibodies recognise ryanodine receptor in skeletal muscle, as well as high molecular weight (k-HMW) protein in kidney microsomes. Like the ryanodine receptor, the k-HMW protein binds 45Ca2+ and sediments as a large complex upon sucrose density-gradient centrifugation. In contrast, the k-HMW protein does not bind ryanodine and is glycosylated. Furthermore, monoclonal and polyclonal antibodies generated against purified k-HMW protein do not recognise skeletal muscle ryanodine receptor. Characterisation of a cDNA clone encoding part of the k-HMW protein revealed that it is likely to be the rabbit homologue of human megalin, an autoimmune antigen in membranous glomerulonephritis. Potential consequences of immunological similarities between ryanodine receptors and megalin are discussed in terms of autoimmune disease.
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:month |
Jun
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pubmed:issn |
1107-3756
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pubmed:author |
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pubmed:issnType |
Print
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pubmed:volume |
3
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
625-32
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:10341294-Amino Acid Sequence,
pubmed-meshheading:10341294-Animals,
pubmed-meshheading:10341294-Antibodies, Monoclonal,
pubmed-meshheading:10341294-Antibody Specificity,
pubmed-meshheading:10341294-Autoantigens,
pubmed-meshheading:10341294-Calcium,
pubmed-meshheading:10341294-Cell Line,
pubmed-meshheading:10341294-Centrifugation, Density Gradient,
pubmed-meshheading:10341294-Chemical Fractionation,
pubmed-meshheading:10341294-Electrophoresis, Polyacrylamide Gel,
pubmed-meshheading:10341294-Glycosylation,
pubmed-meshheading:10341294-Heymann Nephritis Antigenic Complex,
pubmed-meshheading:10341294-Immunoglobulin M,
pubmed-meshheading:10341294-Kidney,
pubmed-meshheading:10341294-Membrane Glycoproteins,
pubmed-meshheading:10341294-Microsomes,
pubmed-meshheading:10341294-Molecular Sequence Data,
pubmed-meshheading:10341294-Muscle, Skeletal,
pubmed-meshheading:10341294-Rabbits,
pubmed-meshheading:10341294-Rats,
pubmed-meshheading:10341294-Ryanodine Receptor Calcium Release Channel,
pubmed-meshheading:10341294-Sequence Analysis, DNA,
pubmed-meshheading:10341294-Sequence Homology, Amino Acid
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pubmed:year |
1999
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pubmed:articleTitle |
Autoimmune antigen megalin displays similarities with skeletal muscle ryanodine receptor/Ca2+ release channel.
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pubmed:affiliation |
Division of Neurophysiology, National Institute for Medical Research, The Ridgeway, Mill Hill, London NW7 1 AA, UK.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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