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: EC:1.6.3.1 (
NADPH oxidase
)
11,281
document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)
To determine whether macrophage differentiation involves increased uptake of vitamin C, or ascorbic acid, we assessed the expression and function of its transporter
SVCT2
during phorbol ester-induced differentiation of human-derived THP-1 monocytes. Induction of THP-1 monocyte differentiation by phorbol 12-myristate 13-acetate (PMA) markedly increased
SVCT2
mRNA, protein, and function. When ascorbate was present during PMA-induced differentiation, the increase in
SVCT2
protein expression was inhibited, but differentiation was enhanced. PMA-induced
SVCT2
protein expression was blocked by inhibitors of protein kinase C (PKC), with most of the affect due to the PKCbetaI and betaII isoforms. Activation of MEK/ERK was sustained up to 48 h after PMA treatment, and the inhibitors completely blocked PMA-stimulated
SVCT2
protein expression, indicating an exclusive role for the classical MAP kinase pathway. However, inhibitors of NF-kappaB activation,
NADPH oxidase
inhibitors, and several antioxidants also partially prevented
SVCT2
induction, suggesting diverse distal routes for control of
SVCT2
transcription. Both known promoters for the
SVCT2
were involved in these effects. In conclusion, PMA-induced monocyte-macrophage differentiation is enhanced by ascorbate and associated with increased expression and function of the
SVCT2
protein through a pathway involving sustained activation of PKCbetaI/II, MAP kinase,
NADPH oxidase
, and NF-kappaB.
...
PMID:Macrophage differentiation increases expression of the ascorbate transporter (SVCT2). 1923 38