Pharmacological disintegration of lipid rafts decreases specific tetramer binding and disrupts the CD3 complex and CD8 heterodimer in human cytotoxic T lymphocytes

Scandinavian Journal of Immunology

Volumn 57, Issue 2, 2003, Pages 99-106

  Uhlin, M ^a   Masucci, M G ^a   Levitsky, V ^a  

^a KAROLINSKA INSTITUTE   (Sweden)

Author keywords

[No Author keywords available]

Indexed keywords

CD3 ANTIGEN; CD8 ANTIGEN; TETRAMER;

ANTIBODY SPECIFICITY; ARTICLE; COMPLEX FORMATION; CYTOTOXIC T LYMPHOCYTE; DRUG RECEPTOR BINDING; HUMAN; HUMAN CELL; LIPID COMPOSITION; LIPID METABOLISM; MEMBRANE PERMEABILITY; MOLECULAR CLONING; PRIORITY JOURNAL; PROTEIN DOMAIN; SIGNAL TRANSDUCTION; T LYMPHOCYTE ACTIVATION; T LYMPHOCYTE SUBPOPULATION;

ANTIBIOTICS, ANTIFUNGAL; ANTIGENS, CD3; ANTIGENS, CD8; BETA-CYCLODEXTRINS; CHOLESTEROL; CYCLODEXTRINS; FILIPIN; FLOW CYTOMETRY; HLA-A ANTIGENS; HUMANS; LYMPHOCYTE ACTIVATION; MEMBRANE MICRODOMAINS; RECEPTORS, ANTIGEN, T-CELL; SIGNAL TRANSDUCTION; T-LYMPHOCYTES, CYTOTOXIC;

EID: 0037326944     PISSN: 03009475     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1365-3083.2003.01188.x     Document Type: Article

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