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Coactivator P300 promotes hepatic steatosis in obesity

Coactivator P300 promotes hepatic steatosis in obesity
共激活剂 P300 促进肥胖患者的肝脂肪变性
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

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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.
期刊论文(4)
专著(0)
科研奖励(0)
会议论文
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
  • 批准号:
    9902424
  • 项目类别:
  • 资助金额:
    $54.79万
  • 财政年份:
    2019
  • 负责人:
    Ling He
  • 依托单位:
Coactivator P300 promotes hepatic steatosis in obesity
  • 批准号:
    9755549
  • 项目类别:
  • 资助金额:
    $57.13万
  • 财政年份:
    2019
  • 负责人:
    Ling He
  • 依托单位:
Coactivator P300 promotes hepatic steatosis in obesity
  • 批准号:
    10365981
  • 项目类别:
  • 资助金额:
    $53.21万
  • 财政年份:
    2019
  • 负责人:
    Ling He
  • 依托单位:
Activation of the cAMP-PKA pathway antagonizes metformin action
  • 批准号:
    9186543
  • 项目类别:
  • 资助金额:
    $36.45万
  • 财政年份:
    2015
  • 负责人:
    Ling He
  • 依托单位:
海外基金