Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Pivot Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Target Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Query: UMLS:C0262471 (
ENT
)
5,307
document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)
The expressions of CNT and
ENT
(concentrative and equilibrative nucleoside transporters) in macrophages are differentially regulated by IFN-gamma (interferon-gamma). This cytokine controls gene expression through
STAT1
-dependent and/or -independent pathways (where
STAT1
stands for signal transduction and activator of transcription 1). In the present study, the role of
STAT1
in the response of nucleoside transporters to IFN-gamma was studied using macrophages from
STAT1
knockout mice. IFN-gamma triggered an inhibition of ENT1-related nucleoside transport activity through
STAT1
-dependent mechanisms. Such inhibition of macrophage growth and ENT1 activity by IFN-gamma is required for DNA synthesis. Interestingly, IFN-gamma led to an induction of the CNT1- and CNT2-related nucleoside transport activities independent of
STAT1
, thus ensuring the supply of extracellular nucleosides for the
STAT1
-independent RNA synthesis. IFN-gamma up-regulated CNT2 mRNA and CNT1 protein levels and down-regulated ENT1 mRNA in both wild-type and
STAT1
knockout macrophages. This is consistent with a
STAT1
-independent, long-term-mediated, probably transcription-dependent, regulation of nucleoside transporter genes. Moreover,
STAT1
-dependent post-transcriptional mechanisms are implicated in the regulation of ENT1 activity. Although nitric oxide is involved in the regulation of ENT1 activity in B-cells at a post-transcriptional level, our results show that
STAT1
-dependent induction of nitric oxide by IFN-gamma is not implicated in the regulation of ENT1 activity in macrophages. Our results indicate that both
STAT1
-dependent and -independent pathways are involved in the regulation of nucleoside transporters by IFN-gamma in macrophages.
...
PMID:Interferon-gamma regulates nucleoside transport systems in macrophages through signal transduction and activator of transduction factor 1 (STAT1)-dependent and -independent signalling pathways. 1286 60