1988
DOI: 10.1084/jem.168.5.1719
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The murine MHC class I genes, H-2Dq and H-2Lq, are strikingly homologous to each other, H-2Ld, and two genes reported to encode tumor-specific antigens.

Abstract: Two phenomena appear to distinguish the D region class I genes from those in the K region in the murine MHC: (a) haplotype disparity in the number of expressed D region class I molecules has been observed; and (b) clines of closely related D region class I molecules among and within mice of different H-2 haplotypes can be defined. Both of these observations have been based on serological and peptide mapping analyses of these molecules. Recent reports using molecular biological approaches have corroborated thes… Show more

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Cited by 67 publications
(54 citation statements)
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“…In contrast, the reciprocal exchange chimeric proteins containing L d residues in the first amino-terminal quarter of the ␣2 (14,19,20), was used in most experiments throughout this report. The use of mAb 28-14-8, which recognizes both empty class I-␤ 2 m heterodimers and peptide-associated class I molecules (12,14,22), eliminates any reagent bias in the above immunoprecipitation studies, since this mAb efficiently immunoprecipitates almost all class I molecules containing the L d ␣3 domain. Nevertheless, mAbs other than mAb 28-14-8, specifically mAbs B22/249, 30-5-7, and 64-3-7, were also used, and when those mAbs were capable of immunoprecipitating these molecules, similar results were obtained as when using mAb 28-14-8 (data not shown).…”
Section: Localization Of the Disparity Between L D And L Q In ␤ 2 M Amentioning
confidence: 99%
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“…In contrast, the reciprocal exchange chimeric proteins containing L d residues in the first amino-terminal quarter of the ␣2 (14,19,20), was used in most experiments throughout this report. The use of mAb 28-14-8, which recognizes both empty class I-␤ 2 m heterodimers and peptide-associated class I molecules (12,14,22), eliminates any reagent bias in the above immunoprecipitation studies, since this mAb efficiently immunoprecipitates almost all class I molecules containing the L d ␣3 domain. Nevertheless, mAbs other than mAb 28-14-8, specifically mAbs B22/249, 30-5-7, and 64-3-7, were also used, and when those mAbs were capable of immunoprecipitating these molecules, similar results were obtained as when using mAb 28-14-8 (data not shown).…”
Section: Localization Of the Disparity Between L D And L Q In ␤ 2 M Amentioning
confidence: 99%
“…The L q transfectant had been generated previously by transfection of DAP-3 with the intact cosmid 33.3 containing the L q gene (14). The L d /L q chimeric molecules were generated using the PCR technique, splicing by overlap extension, developed by Pease and colleagues (30).…”
Section: Cell Linesmentioning
confidence: 99%
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“…The same neu-expressing NIH 3T3 cells were transduced with a murine GM-CSF retrovirus using the same methods for inserting the B7-1 gene to create 3T3neuGM vaccine cells. L-D q cells and L-L q cells are murine fibroblast cell lines transfected with murine H-2D q or -L q , respectively (42). All of the above cell lines were maintained at 37°C and 10% CO 2 in DMEM (Life Technologies, Rockville, MD) supplemented with 10% bovine calf serum (HyClone, Logan, UT), 1% L-glutamine (JRH Biosciences, Lenexa, KS), 1% nonessential amino acids (Sigma-Aldrich, St. Louis, MO), 1% sodium pyruvate (Sigma-Aldrich), and 0.5% penicillin/streptomycin (Sigma-Aldrich).…”
Section: Cell Lines and Mediummentioning
confidence: 99%
“…We initially sought to determine whether the L dspecific 2C T cell clone can recognize the highly related class I MHC molecule L q . H-2L d and H-2L q are highly homologous class I molecules with 98% identity in amino acid sequence (26). Fig.…”
Section: C T Cells Cross-react With L Q /P2ca With Low Aviditymentioning
confidence: 99%