Abstract |
Phospholipase C gamma-1 (PLCgamma1) phosphorylation is a key step in intracellular signal transduction in T cells. We used Hut-78 T lymphoma cells to demonstrate the effect of apicidin on cellular levels of the PLCgamma1 molecule. Using reverse-transcription, real-time quantitative PCR and Western blot analysis, we observed that apicidin reduced the PLCgamma1 transcript and protein contents in Hut-78 T lymphoma cells. Our results indicate that protein synthesis appears to be crucial in the apicidin decrease of PLCgamma1 mRNA steadiness. Moreover, we determined that apicidin reduces the half-life of PLCgamma1 mRNAs from approximately 2 to 4h. Since PLCgamma1 is considered a key molecule in signal transduction in T cells, apicidin may be useful in the treatment of some autoimmune diseases in which autoreactive T cells occur.
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Authors | Szymon Debicki, Paweł P Jagodzinski |
Journal | Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie
(Biomed Pharmacother)
Vol. 63
Issue 7
Pg. 543-7
(Aug 2009)
ISSN: 1950-6007 [Electronic] France |
PMID | 18993024
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Histone Deacetylase Inhibitors
- Peptides, Cyclic
- RNA, Messenger
- apicidin
- Phospholipase C gamma
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Topics |
- Animals
- Blotting, Western
- Cell Line, Tumor
- Histone Deacetylase Inhibitors
- Lymphoma, T-Cell
- Peptides, Cyclic
(pharmacology)
- Phospholipase C gamma
(antagonists & inhibitors, biosynthesis, genetics)
- Phosphorylation
- Polymerase Chain Reaction
- RNA, Messenger
(biosynthesis, genetics)
- Rabbits
- Signal Transduction
(genetics)
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