Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
1
pubmed:dateCreated
1995-8-30
pubmed:abstractText
Previous studies have suggested that the CDR3 genetic element of the heavy chain variable region of autoantibodies is important in determining reactivity against self antigens, particularly against DNA. The lpr mutation was recently found to encode for a defective form of the fas protein, a molecule important for the transmission of the apoptotic signal into cells. Our aim was to determine whether CDR3 elements similar to those described for autoantibody-producing hybridomas derived from lupus-prone strains could be found in the preimmune repertoire of B cells in mice with the lpr mutation. The analysis of the junctions of the VH-C mu functional rearrangements derived by polymerase chain reaction (PCR) amplification of RNA obtained from splenic small, resting cells stimulated with lipopolysaccharide (LPS) from male lpr mice showed that a large proportion of them expressed D genes in the unusual reading frames 2 and 3. Two of the lpr joints were formed by D-D fusions. Similarly, nearly half of the lpr sequences had arginines, an amino acid which promotes binding to dsDNA and is seldom observed in normal junctions. Our results show that the preimmune repertoire of lpr animals has abnormal CDR3 elements which may result from a failure at different levels of selection. The antigen-dependent selection of such elements that leads to the expansion of specific, high-affinity anti-dsDNA antibody-producing clones might depend on other genetic factors not found in the C57B1/6-lpr strains but in the MRL-lpr.
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/7621595-1372394, http://linkedlifedata.com/resource/pubmed/commentcorrection/7621595-1382097, http://linkedlifedata.com/resource/pubmed/commentcorrection/7621595-1489729, http://linkedlifedata.com/resource/pubmed/commentcorrection/7621595-1903427, http://linkedlifedata.com/resource/pubmed/commentcorrection/7621595-1910678, http://linkedlifedata.com/resource/pubmed/commentcorrection/7621595-2017653, http://linkedlifedata.com/resource/pubmed/commentcorrection/7621595-2104919, http://linkedlifedata.com/resource/pubmed/commentcorrection/7621595-2989795, http://linkedlifedata.com/resource/pubmed/commentcorrection/7621595-3480535, http://linkedlifedata.com/resource/pubmed/commentcorrection/7621595-3933987, http://linkedlifedata.com/resource/pubmed/commentcorrection/7621595-518835, http://linkedlifedata.com/resource/pubmed/commentcorrection/7621595-6609979, http://linkedlifedata.com/resource/pubmed/commentcorrection/7621595-7851020, http://linkedlifedata.com/resource/pubmed/commentcorrection/7621595-8496598
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jul
pubmed:issn
0009-9104
pubmed:author
pubmed:issnType
Print
pubmed:volume
101
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
73-7
pubmed:dateRevised
2009-11-18
pubmed:meshHeading
pubmed-meshheading:7621595-Amino Acid Sequence, pubmed-meshheading:7621595-Animals, pubmed-meshheading:7621595-Antibodies, Antinuclear, pubmed-meshheading:7621595-B-Lymphocytes, pubmed-meshheading:7621595-Base Sequence, pubmed-meshheading:7621595-DNA, pubmed-meshheading:7621595-Female, pubmed-meshheading:7621595-Gene Rearrangement, B-Lymphocyte, pubmed-meshheading:7621595-Immunoglobulin Heavy Chains, pubmed-meshheading:7621595-Immunoglobulin M, pubmed-meshheading:7621595-Immunoglobulin Variable Region, pubmed-meshheading:7621595-Lipopolysaccharides, pubmed-meshheading:7621595-Male, pubmed-meshheading:7621595-Mice, pubmed-meshheading:7621595-Mice, Inbred C57BL, pubmed-meshheading:7621595-Mice, Mutant Strains, pubmed-meshheading:7621595-Molecular Sequence Data, pubmed-meshheading:7621595-Receptor-CD3 Complex, Antigen, T-Cell
pubmed:year
1995
pubmed:articleTitle
CDR3 regions in the preimmune VH B cell repertoire of lpr mice.
pubmed:affiliation
Department of Immunology, Wenner-Gren Institute, Arrhenius Laboratories for Natural Sciences, University of Stockholm, Sweden.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't