Mitochondrial uncoupling proteins--facts and fantasies
Language English Country Czech Republic Media print
Document type Journal Article, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, P.H.S., Review
Grant support
TW01487
FIC NIH HHS - United States
PubMed
15119950
Knihovny.cz E-resources
- MeSH
- Down-Regulation MeSH
- Ion Channels MeSH
- Humans MeSH
- Fatty Acids metabolism MeSH
- Membrane Proteins metabolism MeSH
- Mitochondrial Proteins MeSH
- Mitochondria metabolism MeSH
- Brain metabolism MeSH
- Organ Specificity MeSH
- Protein Isoforms metabolism MeSH
- Reactive Oxygen Species metabolism MeSH
- Muscles metabolism MeSH
- Carrier Proteins metabolism MeSH
- Uncoupling Protein 1 MeSH
- Binding Sites MeSH
- Animals MeSH
- Check Tag
- Humans MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Review MeSH
- Research Support, U.S. Gov't, P.H.S. MeSH
- Names of Substances
- Ion Channels MeSH
- Fatty Acids MeSH
- Membrane Proteins MeSH
- Mitochondrial Proteins MeSH
- Protein Isoforms MeSH
- Reactive Oxygen Species MeSH
- Carrier Proteins MeSH
- UCP1 protein, human MeSH Browser
- Uncoupling Protein 1 MeSH
Instead of a comprehensive review, we describe the basic undisputed facts and a modest contribution of our group to the fascinating area of the research on mitochondrial uncoupling proteins. After defining the terms uncoupling, leak, protein-mediated uncoupling, we discuss the assumption that due to their low abundance the novel mitochondrial uncoupling proteins (UCP2 to UCP5) can provide only a mild uncoupling, i.e. can decrease the proton motive force by several mV only. Contrary to this, the highly thermogenic role of UCP1 in brown adipose tissue is not given only by its high content (approximately 5 % of mitochondrial proteins) but also by the low ATP synthase content and high capacity respiratory chain. Fatty acid cycling mechanism as a plausible explanation for the protonophoretic function of all UCPs and some other mitochondrial carriers is described together with the experiments supporting it. The phylogenesis of all UCPs, estimated UCP2 content in several tissues, and details of UCP2 activation are described on the basis of our experiments. Functional activation of UCP2 is proposed to decrease reactive oxygen species (ROS) production. Moreover, reaction products of lipoperoxidation such as cleaved hydroperoxy-fatty acids and hydroxy-fatty acid can activate UCP2 and promote feedback down-regulation of mitochondrial ROS production.
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Cytoprotective activity of mitochondrial uncoupling protein-2 in lung and spleen
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Channel character of uncoupling protein-mediated transport