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1.
FEBS Lett ; 587(21): 3487-94, 2013 Nov 01.
Article in English | MEDLINE | ID: mdl-24036448

ABSTRACT

G-protein-coupled receptor kinase 2 (GRK2) levels are elevated in inflammation but its role is not clear yet. Here we show that GRK2 expression is dependent on NFκB transcriptional activity. In macrophages, LPS induces GRK2 accumulation in mitochondria increasing biogenesis. The overexpression of the carboxy-terminal domain of GRK2 (ßARK-ct), known to displace GRK2 from plasma membranes, induces earlier localization of GRK2 to mitochondria in response to LPS leading to increased mt-DNA transcription and reduced ROS production and cytokine expression. Our study shows the relevance of GRK2 subcellular localization in macrophage biology and its potential therapeutic properties in inflammation.


Subject(s)
G-Protein-Coupled Receptor Kinase 2/metabolism , Inflammation/metabolism , Macrophages/metabolism , Mitochondria/enzymology , Animals , Humans , Lipopolysaccharides/metabolism , Lipopolysaccharides/pharmacology , Mice , Mitochondria/metabolism , Reactive Oxygen Species/metabolism , Signal Transduction
2.
J Appl Physiol (1985) ; 90(1): 389-96, 2001 Jan.
Article in English | MEDLINE | ID: mdl-11133932

ABSTRACT

Mitochondrial transcription factor A (Tfam) is a nuclear-encoded gene product that is imported into mitochondria and is required for the transcription of mitochondrial DNA (mtDNA). We hypothesized that conditions known to produce mitochondrial biogenesis in skeletal muscle would be preceded by an increase in Tfam expression. Therefore, rat muscle was stimulated (10 Hz, 3 h/day). Tfam mRNA levels were significantly elevated (by 55%) at 4 days and returned to control levels at 14 days. Tfam import into intermyofibrillar (IMF) mitochondria was increased by 52 and 61% (P < 0.05) at 5 and 7 days, respectively. This corresponded to an increase in the level of import machinery components. Immunoblotting data indicated that IMF Tfam protein content was increased by 63% (P < 0.05) at 7 days of stimulation. This was associated with a 49% (P < 0.05) increase in complex formation at the mtDNA promoter and a 65% (P < 0.05) increase in the levels of a mitochondrial transcript, cytochrome-c oxidase (COX) subunit III. Similarly, COX enzyme activity was elevated by 71% (P < 0.05) after 7 days of contractile activity. These results indicate that early events in mitochondrial biogenesis include increases in Tfam mRNA, followed by accelerations in mitochondrial import and increased Tfam content, which correspond with increased binding to the mtDNA promoter region. This was accompanied by increased mitochondrial transcript levels and elevated COX activity. These data support the role of Tfam as a regulatory protein involved in contractile activity-induced mitochondrial biogenesis.


Subject(s)
DNA-Binding Proteins , Mitochondrial Proteins , Muscle Contraction/physiology , Nuclear Proteins/metabolism , Transcription Factors/metabolism , Animals , Binding Sites , Biological Transport , DNA/physiology , Male , Mitochondria, Muscle/metabolism , Muscle, Skeletal/metabolism , Myofibrils/metabolism , Nuclear Proteins/genetics , Prostaglandin-Endoperoxide Synthases/metabolism , RNA, Messenger/metabolism , Rats , Rats, Sprague-Dawley , Transcription Factors/genetics
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