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PMID: 2479679 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Activation-driven T cell death. I. Requirements for de novo transcription and translation and association with genome fragmentation.

Journal of immunology (Baltimore, Md. : 1950) ·Vol. 143 ·No. 11 ·1989-12-01 ·Pages 3461-9

Ucker DS, Ashwell JD, Nickas G

Abstract

We have observed that stimuli that are mitogenic for normal T cells can induce cell death in transformed T cell hybridomas. "Activation-driven cell death" can be triggered by the presentation of appropriate Ag as well as by treatment with lectins and antibodies specific for the T cell Ag receptor complex and other activation structures on the T cell surface, such as Thy-1 and Ly-6. The activation-driven lethal process is cell autonomous, is associated with a fragmentation of the cell's genome characteristic of the "suicide process" induced in immature T cells by glucocorticoids and in target cells by cytotoxic T lymphocytes, and is dependent upon transcription and translation, presumably associated with the expression of new gene products. We hypothesize that activation-driven cell death may be involved in vivo in the clonal deletion of auto-reactive T cells during T cell ontogeny.

MeSH Terms
Animals Antibody Specificity Antigens, Ly/immunology Antigens, Surface/immunology Cell Survival Cytotoxicity, Immunologic DNA Damage Epitopes/immunology Hybridomas/immunology,metabolism Kinetics Lectins/immunology Lymphocyte Activation Mice Mice, Inbred BALB C Mice, Inbred CBA Protein Biosynthesis Receptors, Antigen, T-Cell/immunology T-Lymphocytes, Cytotoxic/immunology,metabolism Thy-1 Antigens Transcription, Genetic
Chemicals
Antigens, Ly Antigens, Surface Epitopes Lectins Receptors, Antigen, T-Cell Thy-1 Antigens
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Ucker D S
Division of Immunology, Medical Biology Institute, La Jolla, CA 92037.
Ashwell J D
Nickas G
Article Info
Journal
Journal of immunology (Baltimore, Md. : 1950)
Abbr.
J Immunol
ISSN
0022-1767
Published
1989-12-01
Pages
3461-9
Language
English
Region
United States
NLM ID
2985117R
Subset
IM
Grants
NIGMS NIH HHS · GM 38800 · United States
NIGMS NIH HHS · GM-38385 · United States
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