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Thyroid hormone enhances the ability of serum to accept cellular cholesterol via the ABCA1 transporter.


ABSTRACT: The goal of this study was to examine the effects of thyroid hormone status on the ability of serum to accept cellular cholesterol.Sera from hypophysectomized rats treated ± T(3) was used to evaluate the role of thyroid hormone on serum efflux capacity. 2D-DIGE analysis of serum proteins showed that T(3) treated rats had increased ApoA-I, ApoA-IV and fetuin A levels with decreased Apo E levels. Microarray and real-time RT-PCR analysis of rat liver revealed large increases in ApoA-I, ApoA-IV, ABCG5, and ABCG8 in response to T(3). J774 macrophages, BHK cells, and Fu5AH rat hepatoma cells were used to measure cholesterol efflux mediated by ABCA1, ABCG1 transporters or SR-BI. Sera from T(3)-treated rats stimulated efflux via ABCA1 but not by ABCG1 or SR-BI. Gel filtration chromatography revealed that T(3) treatment caused a decrease in HDL particle size accompanied by higher levels of lipid-poor ApoA-I.Thyroid hormone enhances the ability of serum to accept cellular cholesterol via the ABCA1 transporter. This effect is most likely attributable to increases in small HDL and lipid poor ApoA-I in response to T(3).

SUBMITTER: Boone LR 

PROVIDER: S-EPMC3324859 | biostudies-literature | 2011 Sep

REPOSITORIES: biostudies-literature

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Thyroid hormone enhances the ability of serum to accept cellular cholesterol via the ABCA1 transporter.

Boone Lindsey R LR   Lagor William R WR   Moya Margarita de la Llera Mde L   Niesen Melissa I MI   Rothblat George H GH   Ness Gene C GC  

Atherosclerosis 20110506 1


<h4>Objective</h4>The goal of this study was to examine the effects of thyroid hormone status on the ability of serum to accept cellular cholesterol.<h4>Methods and results</h4>Sera from hypophysectomized rats treated ± T(3) was used to evaluate the role of thyroid hormone on serum efflux capacity. 2D-DIGE analysis of serum proteins showed that T(3) treated rats had increased ApoA-I, ApoA-IV and fetuin A levels with decreased Apo E levels. Microarray and real-time RT-PCR analysis of rat liver re  ...[more]

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