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PMID: 7533644 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Two distinct pathways of specific killing revealed by perforin mutant cytotoxic T lymphocytes.

Immunity ·Vol. 1 ·No. 5 ·1994-08-00 ·Pages 357-64

Kojima H, Shinohara N, Hanaoka S, Someya-Shirota Y, Takagaki Y, Ohno H, Saito T, Katayama T, Yagita H, Okumura K

Abstract

To study the contribution of putative perforin-independent mechanism in the antigen-specific target destruction by cytotoxic T lymphocytes CD8+ CTL lines were established from spleen cells of chimeric mice produced by injecting perforin (-/-) embryonic stem cells into blastocysts of RAG-2(-/-) mice. When tested on normal concanavalin A blasts, these perforin-deficient cytotoxic T lymphocyte lines were found to be capable of inducing antigen-specific target cell lysis accompanied by DNA degradation. In contrast, with target cells carrying a mutation in Fas molecule, perforin-independent cytotoxicity was not detectable. These data not only confirmed the primary role of perforin but simultaneously revealed a major contribution of a perforin-independent Fas-mediated pathway in antigen-specific cytolysis.

MeSH Terms
Animals Antigens, Surface/pharmacology Cell Death/drug effects Cytotoxicity, Immunologic/drug effects Humans Membrane Glycoproteins/genetics,pharmacology Mice Mice, Inbred DBA Mutation Perforin Pore Forming Cytotoxic Proteins T-Lymphocytes, Cytotoxic/cytology,physiology fas Receptor
Chemicals
Antigens, Surface Membrane Glycoproteins Pore Forming Cytotoxic Proteins fas Receptor Perforin
Authors & Affiliations
10 authors, click to expand affiliations / ORCID
Kojima H
Laboratory of Cellular Immunology, Mitsubishi Kasei Institute of Life Sciences, Tokyo, Japan.
Shinohara N
Hanaoka S
Someya-Shirota Y
Takagaki Y
Ohno H
Saito T
Katayama T
Yagita H
Okumura K
Article Info
Journal
Immunity
Abbr.
Immunity
ISSN
1074-7613
Published
1994-08-00
Pages
357-64
Language
English
Region
United States
NLM ID
9432918
Subset
IM
Grants
NIAID NIH HHS · AI20047 · United States
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