Source:http://linkedlifedata.com/resource/pubmed/id/17096877
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
5
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pubmed:dateCreated |
2006-11-13
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pubmed:abstractText |
In order to investigate the inhibition role of anti-Fas hammerhead ribozyme on Fas expression and Fas-mediated apoptosis in CTLL-2 cells (mouse CTL cell line), and to explore a new way for enhancing the ability of T cells against Leukemia in donor lymphocytes infusion, CTLL-2 cells were transfected with pEGFP-RZ596 and pEGFPC1 (mock-transfected) via electroporation. Fas expression on CTLL-2 cells was detected by RT-PCR and Western blot. The killing effect of CTL against WEHI-3 (mouse acute myelomonocytic leukemia cell line) highly expressing FasL in vitro was detected by MTT assay. The caspase-3 proteolytic activity and the apoptosis rate of CTLL-2 cells were detected by means of BD AproAlert Caspase-3 Colorimetric kit and FITC labeled Annexin-V apoptosis detecting kit respectively. The results showed that the anti-Fas ribozyme could be successfully introduced into mouse CTLL-2 cells; Fas expression on the surface of cells transfected with the ribozyme was obviously decreased, in comparison with control and mock-transfected cells; after cocultured with WEHI-3 cells, the viability of CTLL-2 cells transfeced with the ribozyme was significantly increased, as compared with other two groups; caspase-3 activity and apoptosis rate of the ribozyme-transfeced cells were significantly decreased, the killing effect of CTLL-2 transfected with the ribozyme was stronger than that of other groups. It is concluded that anti-Fas ribozyme can remarkably decrease Fas expression on CTLL-2 cells, so as to avoid Fas-mediated apoptosis by Fas ligand on WEHI-3 cells, and to enhance their killing activity against WEHI-3 cells, as a result, the immune escape of acute myelomonocytic leukemia was depressed.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Oct
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pubmed:issn |
1009-2137
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
14
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
862-6
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pubmed:meshHeading |
pubmed-meshheading:17096877-Animals,
pubmed-meshheading:17096877-Cell Line,
pubmed-meshheading:17096877-Fas Ligand Protein,
pubmed-meshheading:17096877-Leukemia, Myelomonocytic, Acute,
pubmed-meshheading:17096877-Mice,
pubmed-meshheading:17096877-RNA, Catalytic,
pubmed-meshheading:17096877-T-Lymphocytes, Cytotoxic,
pubmed-meshheading:17096877-Tumor Cells, Cultured,
pubmed-meshheading:17096877-Tumor Escape
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pubmed:year |
2006
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pubmed:articleTitle |
[Depressing the immune escape of acute myelomonocytic leukemia via an anti-Fas ribozyme].
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pubmed:affiliation |
Institute of Hematology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430022, China. liulinbo@medmail.com.cn
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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