Novel role of cholesteryl ester transfer protein (CETP): attenuation of adiposity by enhancing lipolysis and brown adipose tissue activity

dc.contributorSistema FMUSP-HC: Faculdade de Medicina da Universidade de São Paulo (FMUSP) e Hospital das Clínicas da FMUSP
dc.contributor.authorRAPOSO, Helena F.
dc.contributor.authorFORSYTHE, Patricia
dc.contributor.authorCHAUSSE, Bruno
dc.contributor.authorCASTELLI, Julia Z.
dc.contributor.authorMORAES-VIEIRA, Pedro M.
dc.contributor.authorNUNES, Valeria S.
dc.contributor.authorOLIVEIRA, Helena C. F.
dc.date.accessioned2021-02-18T13:56:55Z
dc.date.available2021-02-18T13:56:55Z
dc.date.issued2021
dc.description.abstractObjective: The systemic function of CETP has been well characterized. CETP plasma activity reduces HDL cholesterol and thus increases the risk of atherosclerosis. Here, we investigated whether CETP expression modulate adiposity. Methods: Body adiposity and energy metabolism related assays and gene/protein expression were compared in CETP transgenic and non-transgenic mice and in hamsters treated with CETP neutralizing antibody. Results: We found that transgenic mice expressing human CETP present less white adipose tissue mass and lower leptinemia than nontransgenic (NTg) littermates. No differences were found in physical activity, food intake, fat fecal excretion, lipogenesis or exogenous lipid accumulation in adipose depots. Nonetheless, adipose lipolysis rates and whole-body energy expenditure were elevated in CETP mice. In accordance, lipolysis-related gene expression and protein content were increased in visceral and brown adipose tissue (BAT). In addition, we verified increased BAT temperature and oxygen consumption. These results were confirmed in two other animal models: 1) hamsters treated with CETP neutralizing antibody and 2) an independent line of transgenic mice expressing simian CETP. Conclusions: These findings reveal a novel anti-adipogenic role for CETP.eng
dc.description.indexMEDLINEeng
dc.identifier.citationMETABOLISM-CLINICAL AND EXPERIMENTAL, v.114, article ID 154429, 14p, 2021
dc.identifier.doi10.1016/j.metabol.2020.154429
dc.identifier.eissn1532-8600
dc.identifier.issn0026-0495
dc.identifier.urihttps://observatorio.fm.usp.br/handle/OPI/39589
dc.language.isoeng
dc.publisherW B SAUNDERS CO-ELSEVIER INCeng
dc.relation.ispartofMetabolism-Clinical and Experimental
dc.rightsrestrictedAccesseng
dc.rights.holderCopyright W B SAUNDERS CO-ELSEVIER INCeng
dc.subjectCETPeng
dc.subjectAdiposityeng
dc.subjectLipolysiseng
dc.subjectOxygen consumptioneng
dc.subjectBrown adipose tissueeng
dc.subject.otherhormone-sensitive lipaseeng
dc.subject.otherdiet-induced obesityeng
dc.subject.othertransgenic miceeng
dc.subject.othergene-expressioneng
dc.subject.othercell-sizeeng
dc.subject.otherhigh-riskeng
dc.subject.otherplasmaeng
dc.subject.otherglucoseeng
dc.subject.otheratherosclerosiseng
dc.subject.othermetabolismeng
dc.subject.wosEndocrinology & Metabolismeng
dc.titleNovel role of cholesteryl ester transfer protein (CETP): attenuation of adiposity by enhancing lipolysis and brown adipose tissue activityeng
dc.typearticleeng
dc.type.categoryoriginal articleeng
dc.type.versionpublishedVersioneng
dspace.entity.typePublication
hcfmusp.author.externalRAPOSO, Helena F.:Univ Estadual Campinas, Dept Struct & Funct Biol, Inst Biol, Campinas, SP, Brazil; Univ Estadual Campinas, Obes & Comorbid Res Ctr, Inst Biol, Campinas, SP, Brazil
hcfmusp.author.externalFORSYTHE, Patricia:Univ Estadual Campinas, Dept Struct & Funct Biol, Inst Biol, Campinas, SP, Brazil
hcfmusp.author.externalCHAUSSE, Bruno:Univ Estadual Campinas, Obes & Comorbid Res Ctr, Inst Biol, Campinas, SP, Brazil
hcfmusp.author.externalCASTELLI, Julia Z.:Univ Estadual Campinas, Dept Struct & Funct Biol, Inst Biol, Campinas, SP, Brazil; Univ Estadual Campinas, Obes & Comorbid Res Ctr, Inst Biol, Campinas, SP, Brazil
hcfmusp.author.externalMORAES-VIEIRA, Pedro M.:Univ Estadual Campinas, Obes & Comorbid Res Ctr, Inst Biol, Campinas, SP, Brazil; Univ Estadual Campinas, Lab Immunometab, Dept Genet Evolut Microbiol & Immunol, Inst Biol, Campinas, SP, Brazil; Univ Estadual Campinas, Expt Med Res Cluster EMRC, Campinas, SP, Brazil
hcfmusp.author.externalOLIVEIRA, Helena C. F.:Univ Estadual Campinas, Dept Struct & Funct Biol, Inst Biol, Campinas, SP, Brazil; Univ Estadual Campinas, Obes & Comorbid Res Ctr, Inst Biol, Campinas, SP, Brazil
hcfmusp.citation.scopus8
hcfmusp.contributor.author-fmusphcVALERIA SUTTI NUNES
hcfmusp.description.articlenumber154429
hcfmusp.description.volume114
hcfmusp.origemWOS
hcfmusp.origem.pubmed33166579
hcfmusp.origem.scopus2-s2.0-85096388578
hcfmusp.origem.wosWOS:000599880200018
hcfmusp.publisher.cityPHILADELPHIAeng
hcfmusp.publisher.countryUSAeng
hcfmusp.relation.referenceAgha G, 2015, INT J EPIDEMIOL, V44, P1277, DOI 10.1093/ije/dyu236eng
hcfmusp.relation.referenceAkbarzadeh M, 2012, MOL BIOL REP, V39, P9529, DOI 10.1007/s11033-012-1817-3eng
hcfmusp.relation.referenceAshrafi K, 2003, NATURE, V421, P268, DOI 10.1038/nature01279eng
hcfmusp.relation.referenceBarter PJ, 2007, NEW ENGL J MED, V357, P2109, DOI 10.1056/NEJMoa0706628eng
hcfmusp.relation.referenceBenoist F, 1997, J BIOL CHEM, V272, P23572, DOI 10.1074/jbc.272.38.23572eng
hcfmusp.relation.referenceBenton MC, 2015, GENOME BIOL, V16, DOI 10.1186/s13059-014-0569-xeng
hcfmusp.relation.referenceBroeders EPM, 2015, CELL METAB, V22, P418, DOI 10.1016/j.cmet.2015.07.002eng
hcfmusp.relation.referenceCannon B, 2011, J EXP BIOL, V214, P242, DOI 10.1242/jeb.050989eng
hcfmusp.relation.referenceCappel DA, 2013, MOL METAB, V2, P457, DOI 10.1016/j.molmet.2013.08.007eng
hcfmusp.relation.referenceCazita PM, 2008, SHOCK, V30, P590, DOI 10.1097/SHK.0b013e31816e30fdeng
hcfmusp.relation.referenceCherezov V, 2007, SCIENCE, V318, P1258, DOI 10.1126/science.1150577eng
hcfmusp.relation.referenceCortes-Martin A, 2020, SCI REP-UK, V10, DOI 10.1038/s41598-020-64833-4eng
hcfmusp.relation.referenceDRAYNA D, 1987, NATURE, V327, P632, DOI 10.1038/327632a0eng
hcfmusp.relation.referenceFerrante AW, 2013, DIABETES OBES METAB, V15, P34, DOI 10.1111/dom.12154eng
hcfmusp.relation.referenceHA YC, 1982, COMP BIOCHEM PHYS B, V71, P265, DOI 10.1016/0305-0491(82)90252-8eng
hcfmusp.relation.referenceHaas JT, 2015, HEPATOLOGY, V62, P1659, DOI 10.1002/hep.28125eng
hcfmusp.relation.referenceHarada LM, 2007, ATHEROSCLEROSIS, V191, P313, DOI 10.1016/j.atherosclerosis.2006.05.036eng
hcfmusp.relation.referenceHildebrandt AL, 2002, J PHARMACOL TOXICOL, V47, P99, DOI 10.1016/S1056-8719(02)00208-3eng
hcfmusp.relation.referenceHolm C, 2003, BIOCHEM SOC T, V31, P1120, DOI 10.1042/BST0311120eng
hcfmusp.relation.referenceHPS3 TIMI55-REVEAl Collaborative, 2017, NEW ENGL J MED, V377, P1217, DOI 10.1056/NEJMoa1706444eng
hcfmusp.relation.referenceHutter E, 2006, EXP GERONTOL, V41, P103, DOI 10.1016/j.exger.2005.09.011eng
hcfmusp.relation.referenceIzem L, 2015, J LIPID RES, V56, P515, DOI 10.1194/jlr.M053678eng
hcfmusp.relation.referenceJIANG XC, 1992, J CLIN INVEST, V90, P1290, DOI 10.1172/JCI115993eng
hcfmusp.relation.referenceJohansson LE, 2012, AM J CLIN NUTR, V96, P196, DOI 10.3945/ajcn.111.020578eng
hcfmusp.relation.referenceLangin D, 2006, PHARMACOL RES, V53, P482, DOI 10.1016/j.phrs.2006.03.009eng
hcfmusp.relation.referenceLe Lay S, 2001, J BIOL CHEM, V276, P16904, DOI 10.1074/jbc.M010955200eng
hcfmusp.relation.referenceLee HJ, 2018, SCI REP-UK, V8, DOI 10.1038/s41598-018-20809-zeng
hcfmusp.relation.referenceLi YH, 2014, LIPIDS HEALTH DIS, V13, DOI 10.1186/1476-511X-13-136eng
hcfmusp.relation.referenceLincoff AM, 2017, NEW ENGL J MED, V376, P1933, DOI 10.1056/NEJMoa1609581eng
hcfmusp.relation.referenceMagdalon J, 2016, BBA-MOL CELL BIOL L, V1861, P430, DOI 10.1016/j.bbalip.2016.02.023eng
hcfmusp.relation.referenceMAROTTI KR, 1993, NATURE, V364, P73, DOI 10.1038/364073a0eng
hcfmusp.relation.referenceMasschelin PM, 2020, FRONT PHYSIOL, V10, DOI 10.3389/fphys.2019.01638eng
hcfmusp.relation.referenceMoraes-Vieira PM, 2016, DIABETES, V65, P1317, DOI 10.2337/db15-1696eng
hcfmusp.relation.referenceNavarro CDC, 2017, FREE RADICAL BIO MED, V113, P190, DOI 10.1016/j.freeradbiomed.2017.09.026eng
hcfmusp.relation.referenceNicholson A, 2010, OBESITY, V18, P1902, DOI 10.1038/oby.2009.477eng
hcfmusp.relation.referenceNunes VS, 2011, CLIN CHIM ACTA, V412, P176, DOI 10.1016/j.cca.2010.09.039eng
hcfmusp.relation.referenceOliveira HCF, 1997, ARTERIOSCL THROM VAS, V17, P1045, DOI 10.1161/01.ATV.17.6.1045eng
hcfmusp.relation.referenceOliveira HCF, 2020, ADV EXP MED BIOL, V1276, P15, DOI 10.1007/978-981-15-6082-8_2eng
hcfmusp.relation.referenceOliveira HCF, 2011, IUBMB LIFE, V63, P248, DOI 10.1002/iub.448eng
hcfmusp.relation.referenceOSONO Y, 1995, J CLIN INVEST, V95, P1124, DOI 10.1172/JCI117760eng
hcfmusp.relation.referenceOsuga J, 2000, P NATL ACAD SCI USA, V97, P787, DOI 10.1073/pnas.97.2.787eng
hcfmusp.relation.referenceRadeau T, 1995, J LIPID RES, V36, P2552eng
hcfmusp.relation.referenceRaposo HF, 2016, LIPIDS HEALTH DIS, V15, DOI 10.1186/s12944-016-0179-6eng
hcfmusp.relation.referenceRaposo HF, 2015, NUTR METAB, V12, DOI 10.1186/s12986-015-0058-6eng
hcfmusp.relation.referenceRautureau Y, 2018, CIRCULATION, V138, P1677, DOI 10.1161/CIRCULATIONAHA.117.031134eng
hcfmusp.relation.referenceRODBELL M, 1964, J BIOL CHEM, V239, P375eng
hcfmusp.relation.referenceSAGGERSON ED, 1988, BIOCHEM J, V251, P701, DOI 10.1042/bj2510701eng
hcfmusp.relation.referenceSalerno AG, 2007, INT J OBESITY, V31, P1586, DOI 10.1038/sj.ijo.0803646eng
hcfmusp.relation.referenceSalerno AG, 2019, BIOCHEM J, V476, P3769, DOI 10.1042/BCJ20190543eng
hcfmusp.relation.referenceSchwartz GG, 2012, NEW ENGL J MED, V367, P2089, DOI 10.1056/NEJMoa1206797eng
hcfmusp.relation.referenceShabalina IG, 2010, BBA-BIOENERGETICS, V1797, P773, DOI 10.1016/j.bbabio.2010.04.007eng
hcfmusp.relation.referenceSHEPHERD D, 1969, BIOCHEM J, V114, P597, DOI 10.1042/bj1140597eng
hcfmusp.relation.referenceTAKAHASHI K, 1993, J CLIN INVEST, V92, P2060, DOI 10.1172/JCI116802eng
hcfmusp.relation.referenceTalbot CPJ, 2018, ATHEROSCLEROSIS, V274, P23, DOI 10.1016/j.atherosclerosis.2018.04.029eng
hcfmusp.relation.referenceTALL AR, 1993, J LIPID RES, V34, P1255eng
hcfmusp.relation.referenceTeran-Garcia M, 2008, ATHEROSCLEROSIS, V196, P455, DOI 10.1016/j.atherosclerosis.2006.12.005eng
hcfmusp.relation.referenceToye AA, 2005, DIABETOLOGIA, V48, P675, DOI 10.1007/s00125-005-1680-zeng
hcfmusp.relation.referenceTsutsumi K, 2001, BIOL PHARM BULL, V24, P579, DOI 10.1248/bpb.24.579eng
hcfmusp.relation.referenceVAUGHAN M, 1962, J BIOL CHEM, V237, P3354eng
hcfmusp.relation.referenceWang JL, 2012, ATHEROSCLEROSIS, V223, P342, DOI 10.1016/j.atherosclerosis.2012.06.003eng
hcfmusp.relation.referenceWatanabe M, 2006, NATURE, V439, P484, DOI 10.1038/nature04330eng
hcfmusp.relation.referenceYao ZP, 2005, ANAL BIOCHEM, V343, P344, DOI 10.1016/j.ab.2005.05.002eng
hcfmusp.relation.referenceZHAO J, 1994, AM J PHYSIOL-CELL PH, V267, pC969eng
hcfmusp.relation.referenceZhou HW, 2006, J LIPID RES, V47, P2011, DOI 10.1194/jlr.M600153-JLR200eng
hcfmusp.scopus.lastupdate2024-05-10
relation.isAuthorOfPublication53de8332-95fd-4c89-a0e5-61aa19ef33cb
relation.isAuthorOfPublication.latestForDiscovery53de8332-95fd-4c89-a0e5-61aa19ef33cb
Arquivos
Pacote Original
Agora exibindo 1 - 1 de 1
Nenhuma Miniatura disponível
Nome:
art_RAPOSO_Novel_role_of_cholesteryl_ester_transfer_protein_CETP_2021.PDF
Tamanho:
1.16 MB
Formato:
Adobe Portable Document Format
Descrição:
publishedVersion (English)