Terminally differentiated plasma cells and mouse T cells do not express major histocompatibility complex (MHC) class II genes although class II gene expression is observed in pre-B and mature B cells as well as in activated human T cells. Transient heterokaryons were prepared and analyzed to investigate the mechanisms of inactivation of MHC class II gene in mouse plasmacytoma cells and mouse T cells. The endogenous MHC class II genes in both mouse plasmacytoma cells and mouse T cells can be reactivated by factors present in B cells. This reactivation of class II gene is also observed by fusion with a human T cell line which expresses MHC class II genes, but not with a class II negative human T cell line. It appears that the loss of MHC class II gene expression during the terminal differentiation of B cells or T cell lineage is due to absence of positive regulatory factor(s) necessary for class II transcription.
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1 November 1992
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November 01 1992
Reactivation of a major histocompatibility complex class II gene in mouse plasmacytoma cells and mouse T cells.
C H Chang,
C H Chang
Howard Hughes Medical Institute, Section of Immunobiology, Yale University School of Medicine, Connecticut 06510.
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W L Fodor,
W L Fodor
Howard Hughes Medical Institute, Section of Immunobiology, Yale University School of Medicine, Connecticut 06510.
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R A Flavell
R A Flavell
Howard Hughes Medical Institute, Section of Immunobiology, Yale University School of Medicine, Connecticut 06510.
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C H Chang
Howard Hughes Medical Institute, Section of Immunobiology, Yale University School of Medicine, Connecticut 06510.
W L Fodor
Howard Hughes Medical Institute, Section of Immunobiology, Yale University School of Medicine, Connecticut 06510.
R A Flavell
Howard Hughes Medical Institute, Section of Immunobiology, Yale University School of Medicine, Connecticut 06510.
Online ISSN: 1540-9538
Print ISSN: 0022-1007
J Exp Med (1992) 176 (5): 1465–1469.
Citation
C H Chang, W L Fodor, R A Flavell; Reactivation of a major histocompatibility complex class II gene in mouse plasmacytoma cells and mouse T cells.. J Exp Med 1 November 1992; 176 (5): 1465–1469. doi: https://doi.org/10.1084/jem.176.5.1465
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