Literature DB >> 2647893

Mixed isotype class II antigen expression. A novel class II molecule is expressed on a murine B cell lymphoma.

J S Spencer1, R T Kubo.   

Abstract

The structures of Ia molecules expressed by two BALB/c B cell lymphoma lines, A20-1.11 (A20) and 2PK3, were analyzed in an effort to explain the differences in antigen-presenting capacity displayed by these cells. Alloreactive T cell hybridomas specific for I-Ad and antigen-specific, I-Ad-restricted T cells responded well to A20 as the APC. The same alloreactive T cell hybridomas responded weakly or not at all to 2PK3 and the responses of the antigen-specific, I-Ad-restricted T cells were consistently lower to antigen presented by 2PK3 as compared with A20. T cells restricted to I-Ed responded equally well to either A20 or 2PK3 as APC. Additionally 2PK3, but not A20, stimulated a strong syngeneic mixed lymphocyte response. Structural analyses of the Ia antigens revealed that I-A and I-E molecules were expressed by A20, whereas an I-E and a novel I-A-like molecule were expressed by 2PK3. The novel class II molecule was affinity purified from 2PK3 cells using an mAb specific for Ad beta (MK-D6), and this molecule was subsequently shown by an RIA to react with an E alpha-specific mAb (14-4-4S) as well. Chain-specific polyclonal antisera raised against I-A and I-E alpha and beta chains indicated that the 2PK3 "I-A" alpha chain reacted in immunoblot with E alpha-specific and not A alpha-specific antisera, whereas the beta chain reacted with A beta- and not E beta-specific antisera. Peptide map and partial amino acid sequence analyses indicated that the "I-A" molecule expressed by 2PK3 represented a mixed isotype structure resulting from the pairing of Ed alpha with Ad beta. By immunofluorescence staining analysis, 2PK3 did not react with an mAb specific for Ad alpha. 2PK3 was capable of limited antigen presentation through the mixed isotype molecule to I-Ad-restricted OVA-specific T cell hybridomas, although the responses induced were low compared with presentation through I-A on A20. Previous descriptions of the expression of mixed isotype class II molecules in the mouse have resulted primarily from DNA-mediated gene transfer experiments. The results presented indicate that a mixed isotype class II molecule can be expressed naturally.

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Year:  1989        PMID: 2647893      PMCID: PMC2189264          DOI: 10.1084/jem.169.3.625

Source DB:  PubMed          Journal:  J Exp Med        ISSN: 0022-1007            Impact factor:   14.307


  38 in total

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Authors:  C M Coeshott; R W Chesnut; R T Kubo; S F Grammer; D M Jenis; H M Grey
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Review 4.  The class II molecules of the human and murine major histocompatibility complex.

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8.  Characterization of the molecules on SJL/J lymphomas which stimulate syngeneic T cells.

Authors:  P H Brown; G J Thorbecke
Journal:  J Immunol       Date:  1985-11       Impact factor: 5.422

9.  Antigen-specific, H-2-restricted helper T cell hybridomas.

Authors:  N W Roehm; P Marrack; J W Kappler
Journal:  J Exp Med       Date:  1982-07-01       Impact factor: 14.307

10.  Imbalanced MHC class II molecule expression at surface of murine B cell lymphomas.

Authors:  M Zijlstra; W L Vasmel; M Voormanns; R E de Goede; H J Schoenmakers; J Nieland; R M Slater; C J Melief
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Authors:  M Matsunaga; K Seki; T Mineta; M Kimoto
Journal:  J Exp Med       Date:  1990-02-01       Impact factor: 14.307

4.  Surface expression of a T cell receptor beta (TCR-beta) chain in the absence of TCR-alpha, -delta, and -gamma proteins.

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5.  In vivo expression and function of hybrid Ia dimers (E alpha A beta) in recombinant and transgenic mice.

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6.  Presentation of antigen by mixed isotype class II molecules in normal H-2d mice.

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7.  Structural requirements for pairing of alpha and beta chains in HLA-DR and HLA-DP molecules.

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8.  A novel family of human leukocyte antigen class II receptors may have its origin in archaic human species.

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