Diverse coactivator recruitment through differential PPARγ nuclear receptor agonism

5 páginas

Autores:
Lizcano Losada, Fernando
Vargas, Diana
Tipo de recurso:
Fecha de publicación:
2013
Institución:
Universidad de la Sabana
Repositorio:
Repositorio Universidad de la Sabana
Idioma:
spa
OAI Identifier:
oai:intellectum.unisabana.edu.co:10818/23945
Acceso en línea:
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3615519/
http://hdl.handle.net/10818/23945
Palabra clave:
DNA binding proteins co-activato
Gene expression
Transcription
Telmisartan
Rights
License
Attribution-NonCommercial-NoDerivatives 4.0 International
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spelling Lizcano Losada, FernandoVargas, Diana5/13/2016 11:322016-05-13T16:32:44Z2013-03-04Lizcano, F., & Vargas, D. (2013). Diverse coactivator recruitment through differential PPARγ nuclear receptor agonism. Genetics and Molecular Biology, 36(1), 134–139. http://doi.org/10.1590/S1415-475720130050000021415-4757http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3615519/http://hdl.handle.net/10818/2394510.1590/S1415-475720130050000025 páginasThe PPARγ nuclear receptor regulates the expression of genes involved in lipid and carbohydrate metabolism, and it has protective effects in some patients with type 2 diabetes. Nevertheless, the therapeutic value of the PPARγ nuclear receptor protein is limited due to the secondary effects of some PPARγ ligands. Because the downstream effects of PPARγ are determined by the binding of specific cofactors that are mediated by ligand-induced conformational changes, we evaluated the differential effects of various ligands on the binding of certain cofactors associated with PPARγ. The ligands used were rosiglitazone for treating type 2 diabetes and telmisartan for treating arterial hypertension. Functional, phenotypic, and molecular studies were conducted on pre-adipocyte 3T3-L1 and functional studies in U2OS cells. The moderating influence of various cofactor families was evaluated using transient transfection assays. Our findings confirm that telmisartan has a partial modulating effect on PPARγ activity compared to rosiglitazone. The cofactors SRC1 and GRIP1 mediate the activity of telmisartan and rosiglitazone and partially determine the difference in their effects. Studying the modulating activity of these cofactors can provide interesting insights for developing new therapeutic approaches for certain metabolic diseases.Publicación sin clasificar en Sherpa Romeoapplication/pdfspaGenetics and Molecular BiologyGenet Mol Biol. 2013 Mar; 36(1): 134–139Attribution-NonCommercial-NoDerivatives 4.0 Internationalhttp://creativecommons.org/licenses/by-nc-nd/4.0/http://purl.org/coar/access_right/c_abf2Universidad de La SabanaIntellectum Repositorio Universidad de La SabanaDNA binding proteins co-activatoGene expressionTranscriptionTelmisartanDiverse coactivator recruitment through differential PPARγ nuclear receptor agonismarticlepublishedVersionhttp://purl.org/coar/version/c_970fb48d4fbd8a85http://purl.org/coar/resource_type/c_6501CC-LICENSElicense_rdflicense_rdfapplication/rdf+xml; charset=utf-81223https://intellectum.unisabana.edu.co/bitstream/10818/23945/2/license_rdf7c9ab7f006165862d8ce9ac5eac01552MD52LICENSElicense.txtlicense.txttext/plain; charset=utf-8498https://intellectum.unisabana.edu.co/bitstream/10818/23945/3/license.txtf52a2cfd4df262e08e9b300d62c85cabMD5310818/23945oai:intellectum.unisabana.edu.co:10818/239452022-05-10 05:17:53.411Intellectum Universidad de la Sabanacontactointellectum@unisabana.edu.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
dc.title.en.fl_str_mv Diverse coactivator recruitment through differential PPARγ nuclear receptor agonism
title Diverse coactivator recruitment through differential PPARγ nuclear receptor agonism
spellingShingle Diverse coactivator recruitment through differential PPARγ nuclear receptor agonism
DNA binding proteins co-activato
Gene expression
Transcription
Telmisartan
title_short Diverse coactivator recruitment through differential PPARγ nuclear receptor agonism
title_full Diverse coactivator recruitment through differential PPARγ nuclear receptor agonism
title_fullStr Diverse coactivator recruitment through differential PPARγ nuclear receptor agonism
title_full_unstemmed Diverse coactivator recruitment through differential PPARγ nuclear receptor agonism
title_sort Diverse coactivator recruitment through differential PPARγ nuclear receptor agonism
dc.creator.fl_str_mv Lizcano Losada, Fernando
Vargas, Diana
dc.contributor.author.none.fl_str_mv Lizcano Losada, Fernando
Vargas, Diana
dc.subject.es_CO.fl_str_mv DNA binding proteins co-activato
Gene expression
Transcription
Telmisartan
topic DNA binding proteins co-activato
Gene expression
Transcription
Telmisartan
description 5 páginas
publishDate 2013
dc.date.issued.none.fl_str_mv 2013-03-04
dc.date.available.none.fl_str_mv 2016-05-13T16:32:44Z
dc.date.accessioned.none.fl_str_mv 5/13/2016 11:32
dc.type.en.fl_str_mv article
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dc.identifier.citation.es_CO.fl_str_mv Lizcano, F., & Vargas, D. (2013). Diverse coactivator recruitment through differential PPARγ nuclear receptor agonism. Genetics and Molecular Biology, 36(1), 134–139. http://doi.org/10.1590/S1415-47572013005000002
dc.identifier.issn.none.fl_str_mv 1415-4757
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dc.identifier.uri.none.fl_str_mv http://hdl.handle.net/10818/23945
dc.identifier.doi.none.fl_str_mv 10.1590/S1415-47572013005000002
identifier_str_mv Lizcano, F., & Vargas, D. (2013). Diverse coactivator recruitment through differential PPARγ nuclear receptor agonism. Genetics and Molecular Biology, 36(1), 134–139. http://doi.org/10.1590/S1415-47572013005000002
1415-4757
10.1590/S1415-47572013005000002
url http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3615519/
http://hdl.handle.net/10818/23945
dc.language.iso.es_CO.fl_str_mv spa
language spa
dc.relation.ispartofseries.none.fl_str_mv Genet Mol Biol. 2013 Mar; 36(1): 134–139
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dc.rights.uri.*.fl_str_mv http://creativecommons.org/licenses/by-nc-nd/4.0/
rights_invalid_str_mv Attribution-NonCommercial-NoDerivatives 4.0 International
http://creativecommons.org/licenses/by-nc-nd/4.0/
http://purl.org/coar/access_right/c_abf2
dc.format.es_CO.fl_str_mv application/pdf
dc.publisher.es_CO.fl_str_mv Genetics and Molecular Biology
dc.source.es_CO.fl_str_mv Universidad de La Sabana
Intellectum Repositorio Universidad de La Sabana
institution Universidad de la Sabana
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