Differentiation of brown adipose tissue and biogenesis of thermogenic mitochondria in situ and in cell culture
Jazyk angličtina Země Nizozemsko Médium print
Typ dokumentu časopisecké články
PubMed
2168211
DOI
10.1016/0005-2728(90)90258-6
PII: 0005-2728(90)90258-6
Knihovny.cz E-zdroje
- MeSH
- buněčná diferenciace MeSH
- fluorescenční mikroskopie MeSH
- hnědá tuková tkáň cytologie enzymologie metabolismus MeSH
- inbrední kmeny potkanů MeSH
- jodidperoxidasa metabolismus MeSH
- křečci praví MeSH
- křeček rodu Mesocricetus MeSH
- krysa rodu Rattus MeSH
- kultivované buňky MeSH
- mitochondrie metabolismus MeSH
- myši inbrední BALB C MeSH
- myši MeSH
- perinatologie MeSH
- protonové ATPasy metabolismus MeSH
- respirační komplex IV metabolismus MeSH
- rozpřahující látky metabolismus MeSH
- termoregulace MeSH
- zvířata MeSH
- Check Tag
- křečci praví MeSH
- krysa rodu Rattus MeSH
- myši MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- jodidperoxidasa MeSH
- protonové ATPasy MeSH
- respirační komplex IV MeSH
- rozpřahující látky MeSH
Differentiation and biogenesis of mitochondria in brown adipose tissue (BAT) was studied in situ and in cell culture by Western blotting, enzyme activity measurements, [35S]methionine incorporation and immunofluorescence microscopy. In different rodent species the perinatal development of BAT thermogenic function resulted from the formation of thermogenic mitochondria which replaced the preexisting nonthermogenic mitochondria. Their biogenesis was characterized by the sudden appearance and rapid increase of the uncoupling protein (UCP), increase of cytochrome oxidase (COX) and decrease of H(+)-ATPase. In primary cell culture, differentiation of precursor cells from mouse BAT to typical multilocular adipocytes was accompanied by increasing content of COX and H(+)-ATPase. A selective synthesis of UCP was induced by activation of beta-adrenergic receptors or by elevated levels of cellular cAMP. UCP was quantitatively incorporated into mitochondria and within 24 h after stimulation reached near physiological concentration. Both in situ and in cell culture, the conditions enabling the expression of UCP gene were accompanied by activation of intracellular thyroxine 5'-deiodinase.
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