Interleukin-1 and interferon-alpha augment interleukin-2 (IL-2) production by distinct mechanisms at the IL-2 mRNA level
Jazyk angličtina Země Nizozemsko Médium print
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
8069932
DOI
10.1006/cimm.1994.1249
PII: S0008-8749(84)71249-4
Knihovny.cz E-zdroje
- MeSH
- aktivace lymfocytů MeSH
- buněčné linie MeSH
- časové faktory MeSH
- exprese genu účinky léků MeSH
- interferon alfa farmakologie MeSH
- interleukin-1 farmakologie MeSH
- interleukin-2 genetika farmakologie MeSH
- interleukin-3 farmakologie MeSH
- interleukin-4 farmakologie MeSH
- interleukin-5 farmakologie MeSH
- interleukin-6 farmakologie MeSH
- lidé MeSH
- messenger RNA genetika MeSH
- techniky in vitro MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- interferon alfa MeSH
- interleukin-1 MeSH
- interleukin-2 MeSH
- interleukin-3 MeSH
- interleukin-4 MeSH
- interleukin-5 MeSH
- interleukin-6 MeSH
- messenger RNA MeSH
The production of interleukin-2 (IL-2) by phytohemaglutinin (PHA)-stimulated cells of human leukemia T cell line MOLT-16 can be significantly increased by interleukin-1 (IL-1) or interferon-alpha (IFN-alpha). The enhancing effect of IL-1 and IFN-alpha on IL-2 production was studied at the IL-2 mRNA level. We show that IL-1 enhances considerably and transiently, with the maximum level between 1 and 2 hr after stimulation, the expression of IL-2 mRNA in the PHA-stimulated cells. The level of IL-2 mRNA declined rapidly within 4 to 6 hr after stimulation in both PHA- and PHA plus IL-1-stimulated cell cultures. On the contrary, IFN-alpha does not elevate the level of IL-2 mRNA above the level in PHA-stimulated cultures, but maintains an enhanced level of IL-2 mRNA in the activated cells for more than 6 hr after stimulation. These observations correlate well with the kinetics of IL-2 protein production into the culture media. The results thus suggest that IL-1 and IFN-alpha may exert an enhancing effect on IL-2 production by distinct mechanisms. In addition, none of the five other lymphokines tested (i.e., IL-2, IL-3, IL-4, IL-5, and IL-6) had any significant effect on IL-2 mRNA expression in the activated MOLT-16 cells.
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