Coactivator P300 promotes hepatic steatosis in obesity
Coactivator P300 promotes hepatic steatosis in obesity
批准号:
10597095
负责人:
Ling He
金额:
$52.39万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2019
资助国家:
美国
项目状态:
未结题
起止时间:
2019-04-01 至 2025-03-31
关键词:
ADD-1 proteinAcetylationAcetyltransferaseAffectBindingChemicalsDataDeacetylaseDefectDevelopmentDiabetes MellitusDiseaseDisease ResistanceDoseE1A-associated p300 proteinEP300 geneEpidemicFatty LiverFatty acid glycerol estersGene ExpressionGeneticGoalsHepaticHepatocyteHigh Fat DietHyperglycemiaIRS1 geneIRS2 geneImpairmentInflammatoryInsulin ReceptorInsulin ResistanceInsulin Signaling PathwayKnockout MiceKnowledgeLinkLiverLysineMapsMediatingMediatorMetabolicMetabolic DiseasesMolecularMusNon-Insulin-Dependent Diabetes MellitusNuclearObese MiceObesityOvernutritionPIK3CG genePathway interactionsPatientsPlayPopulationProteinsResveratrolRiskRoleSIRT1 geneSiteTestingTherapeuticTissuesTriglyceridesTyrosine PhosphorylationXBP1 genebiological adaptation to stresscytokineendoplasmic reticulum stressexperimental studyfatty liver diseaseglucose metabolismimprovedin vivoinhibitorinsulin sensitivityinsulin signalinglipid biosynthesislipid metabolismnegative affectnew therapeutic targetnon-alcoholic fatty liver diseasenovelobese patientsoverexpressionp300/CBP-Associated Factorpreventsmall hairpin RNAtherapeutic target
中文摘要
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英文摘要
Obesity, which has reached epidemic proportions worldwide, is associated with an increased risk of numerous
metabolic abnormalities including nonalcoholic fatty liver disease (NAFLD) and type 2 diabetes (T2D). NAFLD
is increasingly common, and now affects over 30% of the population in the USA. Insulin resistance is a hallmark
of type 2 diabetes and obesity, and excessive accumulation of triglycerides is a hallmark of NAFLD. Because
intact insulin signaling is required for lipogenesis, the defect in insulin signaling should reduce hepatic triglyceride
content; however, patients with obesity and type 2 diabetes commonly have nonalcoholic fatty liver disease
(NAFLD), and the majority of patients with NAFLD are also obese and/or have T2D. The underlying mechanisms
leading to the paradoxical co-occurrence of hepatic steatosis and insulin resistance are not well understood.
Previous studies have shown that overexpression of the deacetylase Sirtuin 1 or treatment with resveratrol, a
Sirtuin 1 activator, not only improved hepatic steatosis, but also restored insulin sensitivity in tissues with insulin
resistance. These results suggest that an acetyltransferase can antagonize Sirtuin 1’s activity, causing hepatic
steatosis and insulin resistance. We observed a significant increase in hepatic acetyltransferase P300’s protein
levels in high-fat diet (HFD) fed mice and ob/ob mice through the IRE1-XBP1s pathway in the endoplasmic
reticulum stress response. Depletion of P300 or inhibition of P300 acetyltransferase activity decreased lipogenic
gene expression and increased insulin sensitivity. Therefore, P300 uniquely increases lipogenesis and disrupts
insulin signaling in the liver of obesity. We will assess the role of elevated P300 in promoting hepatic lipogenesis
in Aim 1. We will define the molecular mechanisms of P300’s promotion of hepatic steatosis in Aim 2. We propose
to determine whether P300 acetyltransferase activity is a therapeutic target for obesity/T2D in Aim 3. We believe
that P300 plays an important role in the development of NAFLD and insulin resistance, linking inflammatory and
metabolic diseases.
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DOI:
10.1097/hc9.0000000000000174
发表时间:
2023-07-01
期刊:
Hepatology communications
影响因子:
5.1
作者:
[]
通讯作者:
Mitochondria in Early Life.
生命早期的线粒体。
DOI:
10.2174/1573396319666221221110728
发表时间:
2023
期刊:
Current pediatric reviews
影响因子:
2
作者:
[He,Ling, Maheshwari,Akhil]
通讯作者:
Maheshwari,Akhil
DOI:
10.5005/jp-journals-11002-0013
发表时间:
2022-01
期刊:
Newborn (Clarksville, Md.)
影响因子:
--
作者:
[Peng J, Ramatchandirin B, Pearah A, Maheshwari A, He L]
通讯作者:
He L
DOI:
10.4103/1673-5374.385286
发表时间:
2024-05
期刊:
Neural regeneration research
影响因子:
6.1
作者:
[Loan A, Syal C, Lui M, He L, Wang J]
通讯作者:
Wang J
Coactivator P300 promotes hepatic steatosis in obesity
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批准号:9902424
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依托单位:
Coactivator P300 promotes hepatic steatosis in obesity
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Coactivator P300 promotes hepatic steatosis in obesity
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Activation of the cAMP-PKA pathway antagonizes metformin action
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Activation of the cAMP-PKA pathway antagonizes metformin action
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The Distinct Role of CBP and p300 in Regulating Hepatic Glucose Production
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The Distinct Role of CBP and p300 in Regulating Hepatic Glucose Production
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批准号:8328726
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财政年份:2011
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The Distinct Role of CBP and p300 in Regulating Hepatic Glucose Production
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批准号:8515392
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项目类别:
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财政年份:2011
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依托单位:
The Distinct Role of CBP and p300 in Regulating Hepatic Glucose Production
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批准号:7989326
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项目类别:
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资助金额:$9.0万
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财政年份:2010
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依托单位:
The Distinct Role of CBP and p300 in Regulating Hepatic Glucose Production
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批准号:8115793
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项目类别:
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资助金额:$9.0万
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财政年份:2010
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负责人:Ling He
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依托单位:
海外基金