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 Reske

subject

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 cellCD8

description

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.

10.1111/j.1365-3083.1988.tb02327.xhttps://pubmed.ncbi.nlm.nih.gov/2963370