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Predicate | Object |
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rdf:type | |
lifeskim:mentions |
umls-concept:C0002085,
umls-concept:C0007600,
umls-concept:C0017262,
umls-concept:C0019728,
umls-concept:C0019742,
umls-concept:C0162735,
umls-concept:C0205160,
umls-concept:C0205314,
umls-concept:C0242610,
umls-concept:C0596988,
umls-concept:C0679622,
umls-concept:C1171362,
umls-concept:C1333899,
umls-concept:C1412936,
umls-concept:C1515670,
umls-concept:C1519613,
umls-concept:C2924612
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pubmed:issue |
6
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pubmed:dateCreated |
1992-4-9
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pubmed:databankReference | |
pubmed:abstractText |
The HLA-A,B negative mutant cell line C1R is widely used as a transfection recipient in functional studies of class I MHC genes. It was derived from a normal B cell line, Hmy2, by three rounds of mutagenesis and immunoselection with anti-HLA mAb. Serology characterizes C1R to be negative for the HLA-A2, A3, B35, Bw62, and Cw3 Ag of the parental cell line while retaining expression of HLA-Cw4. We find, however, that CTL specific for HLA-B35 lyse C1R cells, suggesting that expression of HLA-B35 is also retained. To resolve this paradox we examined the expression of HLA-A,B,C genes and proteins in C1R cells. The results are consistent with deletion of the HLA-A3, Bw62, Cw3 haplotype and retention of the HLA-A2, B35, Cw4 haplotype in C1R. Although present, the HLA-A2 gene appears not to be transcribed. As expected, the HLA-Cw4 gene is transcribed and the protein expressed at normal levels. Transcription of the HLA-B35 gene is also normal and comparable to that of HLA-Cw4. However, expression of the HLA-B35 protein is reduced to a few percent of the parental level. Comparison of the nucleotide sequence of B35 alleles from C1R and Hmy2 revealed that reduced translation in C1R is caused by a point mutation (ATG to TTG) in the translation initiation codon. The HLA-B35 allele from C1R and Hmy2 represents a novel subtype, B*3503, differing from B*3501 by replacement of serine by phenylalanine at the peptide binding position 116. This study shows cell surface levels of a class I molecule which are insensitive to lysis by antibody and complement can be readily recognized by alloreactive T cells, further illustrating the relative sensitivity of Ag recognition by T cells.
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
AIM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Mar
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pubmed:issn |
0022-1767
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
15
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pubmed:volume |
148
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1941-8
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pubmed:dateRevised |
2007-11-14
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pubmed:meshHeading |
pubmed-meshheading:1541831-Alleles,
pubmed-meshheading:1541831-Amino Acid Sequence,
pubmed-meshheading:1541831-Base Sequence,
pubmed-meshheading:1541831-Blotting, Southern,
pubmed-meshheading:1541831-Cell Line,
pubmed-meshheading:1541831-Gene Expression,
pubmed-meshheading:1541831-Genes,
pubmed-meshheading:1541831-HLA-A2 Antigen,
pubmed-meshheading:1541831-HLA-B35 Antigen,
pubmed-meshheading:1541831-Humans,
pubmed-meshheading:1541831-Molecular Sequence Data,
pubmed-meshheading:1541831-Mutation,
pubmed-meshheading:1541831-Peptide Chain Initiation, Translational,
pubmed-meshheading:1541831-RNA Splicing,
pubmed-meshheading:1541831-Sequence Alignment,
pubmed-meshheading:1541831-T-Lymphocytes, Cytotoxic
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pubmed:year |
1992
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pubmed:articleTitle |
The HLA-A,B "negative" mutant cell line C1R expresses a novel HLA-B35 allele, which also has a point mutation in the translation initiation codon.
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pubmed:affiliation |
Department of Cell Biology, Stanford University, CA 94305-5400.
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pubmed:publicationType |
Journal Article,
Comparative Study,
Research Support, U.S. Gov't, P.H.S.,
Research Support, Non-U.S. Gov't
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