6533b85bfe1ef96bd12bab72
RESEARCH PRODUCT
Identification of transcripts of the T cell antigen receptor beta chain gene and major histocompatibility complex class II genes in antigen-presenting cloned BK-BI-2.6.C6 cells.
Rück GSteinlein PA. B. Reske-kunzKonrad Reskesubject
HybridomasT cellReceptors Antigen T-Cell alpha-betaT-LymphocytesImmunologyT-cell receptorAntigen presentationHistocompatibility Antigens Class IIReceptors Antigen T-CellAntigen-Presenting CellsGeneral MedicineMHC restrictionBiologyMajor histocompatibility complexMolecular biologyCell LineMicemedicine.anatomical_structurebiology.proteinmedicineCytotoxic T cellAnimalsRNA MessengerAntigen-presenting cellCD8description
The cloned murine cell line BK-BI-2.6.C6 has previously been shown to exhibit T cell characteristics, to synthesize and express MHC class II molecules, and to present protein antigens to antigen-dependent T cell clones. As a more definitive proof of the T-cell nature of these cells, transcripts of the rearranged T cell antigen receptor (TcR) beta gene were assessed by Northern blot analysis. BK-BI-2.6.C6 cells constitutively transcribe mRNA for the light chain of TcR and express the disulphide-linked alpha, beta TcR heterodimer at the cell surface. In addition mRNA for the polymorphic MHC class II subunits A alpha and A beta as well as for the invariant gamma chain were detected. BK-BI-2.6.C6 T cells effectively stimulated bovine insulin-reactive T hybridoma cells to lymphokine production in the presence of this antigen. Since the antigen-presenting and the responding T cell populations are maintained in culture in the absence of feeder cells, contamination by conventional accessory cells is excluded. These data unequivocally demonstrate that cloned murine Ia-expressing T cells can act as antigen-presenting accessory cells.
year | journal | country | edition | language |
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1988-01-01 | Scandinavian journal of immunology |