Synthesis of mitochondrial uncoupling protein in brown adipocytes differentiated in cell culture
Jazyk angličtina Země Spojené státy americké Médium print
Typ dokumentu časopisecké články
PubMed
2176208
PII: S0021-9258(18)45690-6
Knihovny.cz E-zdroje
- MeSH
- 2D gelová elektroforéza MeSH
- buněčná diferenciace MeSH
- hnědá tuková tkáň cytologie metabolismus MeSH
- iontové kanály MeSH
- kinetika MeSH
- kultivované buňky MeSH
- membránové proteiny biosyntéza izolace a purifikace MeSH
- methionin metabolismus MeSH
- mitochondriální proteiny MeSH
- mitochondrie metabolismus MeSH
- myši inbrední BALB C MeSH
- myši MeSH
- protonové ATPasy biosyntéza izolace a purifikace MeSH
- radioizotopy síry MeSH
- respirační komplex IV biosyntéza izolace a purifikace MeSH
- transportní proteiny * MeSH
- uncoupling protein 1 MeSH
- zvířata MeSH
- Check Tag
- myši MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- iontové kanály MeSH
- membránové proteiny MeSH
- methionin MeSH
- mitochondriální proteiny MeSH
- protonové ATPasy MeSH
- radioizotopy síry MeSH
- respirační komplex IV MeSH
- transportní proteiny * MeSH
- uncoupling protein 1 MeSH
In order to characterize the biogenesis of unique thermogenic mitochondria of brown adipose tissue, differentiation of precursor cells isolated from mouse brown adipose tissue was studied in cell culture. Synthesis of mitochondrial uncoupling protein (UCP), F1-ATPase, and cytochrome oxidase was examined by L-[35S]methionine labeling and immunoblotting. For the first time, synthesis of physiological amounts of the UCP, a key and tissue-specific component of thermogenic mitochondria, was observed in cultures at about confluence (day 6), indicating that a complete differentiation of brown adipocytes was achieved in vitro. In postconfluent cells (day 8) the content of UCP decreased rapidly, in contrast to some other mitochondrial proteins (beta subunit of F1-ATPase, cytochrome oxidase). In these cells, it was possible, by using norepinephrine, to induce specifically the synthesis of the UCP but not of F1-ATPase or cytochrome oxidase. The maximal response was observed at 0.1 microM norepinephrine and the synthesis of UCP remained activated for at least 24 h. Detailed analysis revealed a major role of the beta-adrenergic receptors and elevated intracellular concentration of cAMP in stimulation of UCP synthesis. A quantitative recovery of the newly synthesized UCP in the mitochondrial fraction indicated completed biogenesis of functionally competent thermogenic mitochondria.