Abstract |
Expression of human interleukin (IL)-24 in tumors achieved anti- tumor effects through apoptosis. IL-24 also induced secretion of proinflammatory cytokines, suggesting the role in immunity. We showed that murine IL-24 transcripts started from the second initiation codon and that expressed mIL-24 in tumors failed to induce apoptosis. Proliferation of murine cells expressing mIL-24 was the same as that of the parent cells and inoculation of the mIL-24-expressing tumors into syngeneic mice did not produce anti- tumor effects. Secretory mIL-24 did not induce the expression of the IL-6, TNF-α or IFN-γ gene in spleen cells. Expression of mIL-24 receptor subunits, IL-22R and IL-20R1, was undetectable in spleen cells even though they were stimulated by anti-CD3, anti-CD40 antibody or concanavalin A. Transduction of murine tumors with adenoviruses expressing the human IL-24 gene however suppressed the viability and decreased the tumor growth. These data suggest that mIL-24 is functionally irrelevant to the human counterpart.
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Authors | Hiroyasu Nagakawa, Osamu Shimozato, Ling Yu, Akihiko Wada, Kiyoko Kawamura, Quanhai Li, Sunil Chada, Yuji Tada, Yuichi Takiguchi, Koichiro Tatsumi, Masatoshi Tagawa |
Journal | Cellular immunology
(Cell Immunol)
2012 Jan-Feb
Vol. 275
Issue 1-2
Pg. 90-7
ISSN: 1090-2163 [Electronic] Netherlands |
PMID | 22475191
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Copyright | Copyright © 2012 Elsevier Inc. All rights reserved. |
Chemical References |
- Cytokines
- Il24 protein, mouse
- Interleukins
- interleukin-24
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Topics |
- Amino Acid Sequence
- Animals
- Apoptosis
- Cell Line
- Cytokines
(chemistry, genetics, immunology)
- Female
- Gene Expression Regulation
- Humans
- Interleukins
(genetics, immunology)
- Mice
- Molecular Sequence Data
- Neoplasms
(genetics, immunology, pathology)
- Sequence Alignment
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