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. 1987 Jul;84(14):4969-73.
doi: 10.1073/pnas.84.14.4969.

Expression of members of immunoglobulin gene family in somatic cell hybrids between human B and T cells

Expression of members of immunoglobulin gene family in somatic cell hybrids between human B and T cells

D Kozbor et al. Proc Natl Acad Sci U S A. 1987 Jul.

Abstract

Somatic cell hybrids were obtained between human T and B cells and tested for the expression of differentiated traits of both cell lineages. The T-cell parent SUP-T1 is CD3-, CD4+, CD1+, CD8+, is weakly positive for HLA class I determinants, and has an inversion of chromosome 14 due to a site-specific recombination event between an immunoglobulin heavy-chain variable gene and the joining segment of the T-cell receptor alpha chain. The B-cell parent, the 6-thioguanine- and ouabain-resistant mutant GM1500, is a lymphoblastoid cell line that secretes IgG2, kappa chains, and expresses B1, B532, and HLA class I and II antigens. All hybrids expressed characteristics of B cells (Ig+, B1+, B532+, EBNA+, HLA antigens), whereas only CD4 among the T-cell markers was expressed. The level of T-cell receptor beta-chain transcript was greatly reduced and no RNA of the chimeric T-cell receptor alpha-chain joining segment-immunoglobulin heavy-chain variable region was detected. Southern blot analysis indicated that absence of T-cell differentiation markers in the hybrids was not due to chromosomal loss. Rather, some B-cell-specific factor present in the hybrids may account for the suppression.

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References

    1. Int J Cancer. 1978 Jun 15;21(6):707-19 - PubMed
    1. Cell. 1978 May;14(1):9-20 - PubMed
    1. Cell. 1980 Apr;19(4):821-7 - PubMed
    1. Science. 1980 Jul 25;209(4455):520-1 - PubMed
    1. Proc Natl Acad Sci U S A. 1980 Sep;77(9):5201-5 - PubMed

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