NDLI: T-cell receptor-CD4 physical association in a murine T-cell hybridoma: induction by antigen receptor ligation.

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T-cell receptor-CD4 physical association in a murine T-cell hybridoma: induction by antigen receptor ligation.

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Specific photoaffinity labeling of two plasma membrane polypeptides with an azido auxin.

Phytochrome induces changes in the immunodetectable level of a wall peroxidase that precede growth changes in maize seedlings.

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T-cell receptor-CD4 physical association in a murine T-cell hybridoma: induction by antigen receptor ligation.

Content Provider	World Health Organization (WHO)-Global Index Medicus
Author	Goldman, S. J. Burakoff, S. J. Mittler, R. S. Spitalny, G. L.
Description	Author Affiliation: Mittler RS ( Bristol-Myers Co., Pharmaceutical Research and Development Division, Wallingford, CT 06492-7660.);
Abstract	By employing flow cytometric analysis and fluorescence resonance energy transfer (FRET), we examined the physical relationship between the T-cell receptor-CD3 complex (Ti-CD3) and the CD4 molecule on helper T cells. Through the use of an L3T4-negative murine T-cell hybridoma infectant expressing the human CD4 gene and having antigen specificity for HLA-DR, we show that binding of the Ti-CD3 complex with an anti-CD3 monoclonal antibody induces its redistribution proximal to cell-surface CD4. FRET efficiency was 9.4% on cells labeled with rhodaminated anti-CD3 and fluoresceinated anti-CD4. FRET was found to be temperature dependent, since similarly treated cells held at 4 degrees C displayed a FRET efficiency of less than 1%. Energy transfer was evident within 3 min after warming cells to 37 degrees C. Energy transfer was not detected between Ti-CD3 and the abundantly expressed leukocyte common antigen (CD45). Of greater significance was our observation that hybridomas infected with a truncated CD4 gene lacking the cytoplasmic domain failed to transfer energy despite the fact that CD4 was expressed on the cell surface at levels equivalent to or greater than the wild type. These studies suggest that after crosslinking of the Ti-CD3 on CD4+ T cells, a physical association occurs between the antigen receptor complex and CD4 and that the association is dependent upon the presence of the cytoplasmic domain of CD4.
ISSN	00278424
e-ISSN	10916490
Journal	Proceedings of the National Academy of Sciences of the United States of America
Issue Number	21
Volume Number	86
Language	English
Publisher	National Academy of Sciences
Publisher Date	1989-12-01
Publisher Place	United States
Access Restriction	Open
Subject Keyword	Antigens, CD4 Immunology Receptors, Antigen, T-Cell T-Lymphocytes Animals Antibodies Antibodies, Monoclonal Energy Transfer Flow Cytometry Fluorescent Dyes Hybridomas Immunoglobulin Fab Fragments Kinetics Mice T-Lymphocytes, Helper-Inducer Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S. Multidisciplinary
Content Type	Text
Resource Type	Article
Subject	Multidisciplinary

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