3,5-diiodo-L-thyronine upregulates rat-liver mitochondrial F(o)F(1)-ATP synthase by GA-binding protein/nuclear respiratory factor-2.
Abstract
Besides triiodothyronine (T3), 3,5-diiodo-l-thyronine (T2) has been reported to affect mitochondrial bioenergetic parameters. T2 effects have been considered as independent of protein synthesis. Here, we investigated the effect of in vivo chronic T2 administration to hypothyroid rats on liver mitochondrial FoF1-ATP synthase activity and expression. T2 increased state 4 and state 3 oxygen consumption and raised ATP synthesis and hydrolysis, which were reduced in hypothyroid rats. Immunoblotting analysis showed that T2 up-regulated the expression of several subunits (α, β, FoI-PVP and OSCP) of the ATP synthase. The observed increase of β-subunit mRNA accumulation suggested a T2-mediated nuclear effect. Then, the molecular basis underlying T2 effects was investigated. Our results support the notion that the β-subunit of ATP synthase is indirectly regulated by T2 through, at least in part, the activation of the transcription factor GA-binding protein/nuclear respiratory factor-2. These findings provide new insights into the T2 role on bioenergetic mechanisms.
Autore Pugliese
Tutti gli autori
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Mangiullo R. , Gnoni A. , Damiano F. , Siculella L. , Zanotti F. , Papa S. , Gnoni G.V.
Titolo volume/Rivista
BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS
Anno di pubblicazione
2010
ISSN
0005-2728
ISBN
Non Disponibile
Numero di citazioni Wos
25
Ultimo Aggiornamento Citazioni
28/04/2018
Numero di citazioni Scopus
26
Ultimo Aggiornamento Citazioni
28/04/2018
Settori ERC
Non Disponibile
Codici ASJC
Non Disponibile
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