Increased cytolytic T lymphocyte activity induced by 2-mercaptoethanol in mixed leukocyte cultures: kinetics and possible mechanisms of action

Details

Serval ID
serval:BIB_871175595FCC
Type
Article: article from journal or magazin.
Collection
Publications
Institution
Title
Increased cytolytic T lymphocyte activity induced by 2-mercaptoethanol in mixed leukocyte cultures: kinetics and possible mechanisms of action
Journal
Journal of Immunology
Author(s)
Harris  J. W., MacDonald  H. R., Engers  H. D., Fitch  F. W., Cerottini  J.
ISSN
0022-1767 (Print)
Publication state
Published
Issued date
04/1976
Volume
116
Number
4
Pages
1071-7
Notes
Journal Article
Research Support, U.S. Gov't, Non-P.H.S. --- Old month value: Apr
Abstract
The 20- to 50-fold increase in cytolytic T lymphocyte (CTL) activity caused by the addition of 50 muM 2-mercaptoethanol (2-ME) at the onset of a one-way murine mixed leukocyte culture (MLC) between C57BL/6 and DBA/2 splenic lymphocytes appears to be unrelated to early events in the culture: if 2-ME was present for the first 24 hr of culture only, there was no increase on day 4, but if addition of 2-ME was delayed until the last 24 hr of culture, the CTL activity was almost as high as that of cultures that were exposed to 2-ME for the entire 4-day culture period. The increase of CTL activity caused by delayed addition of 2-ME ("2-ME rescue") was used to investigate the mechanism by which the thiol induces differentiation of CTL from precursor cells. 2-ME rescue was mimicked by two other thiols, dithiothreitol and cysteamine phosphate, but at higher concentrations. Because the latter compound has no free sulhydryl group until it diffuses into cells and is enzymatically dephosphorylated, we conclude that thiols may increase the differentiation of CTL from precursor cells by an intracellular process involving free sulphydryl groups rather than by interaction with membrane sulfhydryls or destruction of inhibitor cells or their products. Cell separation experiments indicated that 2-ME rescue was independent of the presence of B lymphocytes and of adherent cells (macrophages) and was restricted to a subpopulation of T lymphocytes that developed into large lymphoid precursor cells during the first 3 days in culture even without 2-ME. The development of this subpopulation required DNA synthesis between 24 nad 72 hr after the onset of MLC. When 2-ME was added to day-3 MLC, CTL activity increased slightly as early as 4 hr later, but the major increase occurred during the second half of the 24 hr "rescue"period. Because this increase was inhibited by cytosine arabinoside (ARA-C), it seems likely that DNA synthesis is associated with and may be required for the differentiation of large precursor lymphoid cells into CTL after the addition of 2-ME.
Keywords
Animals B-Lymphocytes/metabolism Cell Separation Cytarabine/pharmacology Cytotoxicity Tests, Immunologic DNA/biosynthesis Dithiothreitol/pharmacology Kinetics Lymphocyte Culture Test, Mixed Macrophages/metabolism Mercaptoethanol/*pharmacology Mice Mice, Inbred C57BL Mice, Inbred DBA T-Lymphocytes/*immunology Time Factors
Pubmed
Web of science
Create date
28/01/2008 11:13
Last modification date
20/08/2019 14:46
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