Abstract
Antigen-specific cytolysis by major histocompatibility complex (MHC) class II-restricted cloned T-cell lines was found to be dependent on protein synthesis. Cytolysis by both polyclonal short-term and long-term class I-restricted cytotoxic T lymphocytes (CTL) was almost completely insensitive to inhibitors of protein synthesis. Kinetic studies with class II-restricted CTL indicated that approximately 2-3 hr after initiation of activation, resistance to inhibitors of protein synthesis was acquired. This strongly suggests that either a cytotoxic effector molecule or an intermediary important in the delivery of such a molecule is synthesized rapidly after activation in class II-restricted CTL, whilst class I-restricted CTL have no such requirement.
MeSH Terms
Animals
Cell Line
Cycloheximide/pharmacology
Cytotoxicity, Immunologic/drug effects,immunology
Dactinomycin/pharmacology
Female
Genes, MHC Class II/immunology
Lymphocyte Activation/immunology
Major Histocompatibility Complex/immunology
Mice
Mice, Inbred Strains
Protein Biosynthesis
T-Lymphocytes, Cytotoxic/immunology,metabolism
Chemicals
Dactinomycin
Cycloheximide
Authors & Affiliations
1 authors, click to expand affiliations / ORCID
Tite J P
Department of Molecular Biology, Wellcome Biotech, Beckenham, Kent, U.K.
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