Obesity is associated with a state of chronic inflammation that is thought to be a major contributor to diabetes and atherosclerosis. Many inflammatory pathways that contribute to the development of insulin resistance and atherosclerosis are regulated by IKK?/NF-?B signaling. However, the role of IKK? in metabolic disorders and atherosclerosis remains elusive. Our initial studies showed that IKK? deficiency (driven by a SM22Cre-IKK?- flox system) in smooth muscle cells (SMCs) rendered mice resistant to the development of diet-induced obesity, metabolic disorders, and atherosclerosis. We made the novel finding that SM22 is expressed in primary adipose stromal vascular (SV) cells and IKK? positively regulates adipogenesis, indicating that chronic inflammation might be an important initial trigger for the adipocyte differentiation in response to high-fat diet consumption. Our central hypothesis is that IKK? is essential for adipogenesis and atherogenesis, and that high-fat diet-induced IKK? activation promotes adipocyte differentiation and adipose inflammation, leading to increased obesity, insulin resistance, and atherosclerosis.
Three specific aims are proposed: (1) Define the role of IKK? in the regulation of murine and human adipocyte differentiation in response to overnutrition; (2) Determine the contribution of adipocyte IKK? to the development of obesity-associated insulin resistance and atherosclerosis; and (3) Determine the impact of pharmacological inhibition of IKK? by antisense oligonucleotides on diet-induced obesity and atherosclerosis. The proposed studies will define the role of IKK? in adipogenesis and atherogenesis and will reveal a critical link between overnutrition, inflammation, and cardiometabolic disease. Our studies will also provide strong evidence for use of appropriate IKK? inhibitors as an innovative therapeutic strategy to treat obesity and cardiometabolic disease.

Public Health Relevance

Obesity is a rapidly growing epidemic representing a serious threat to the health of the population in almost every country around the world. There is an urgent need to understand the mechanisms underlying the diet- induced obesity and associated cardiometabolic disease. The proposed study will investigate a novel mechanism that links overnutrition to obesity and metabolic disorders.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Project (R01)
Project #
5R01HL131925-03
Application #
9438565
Study Section
Vascular Cell and Molecular Biology Study Section (VCMB)
Program Officer
Kirby, Ruth
Project Start
2016-04-01
Project End
2020-02-29
Budget Start
2018-03-01
Budget End
2019-02-28
Support Year
3
Fiscal Year
2018
Total Cost
Indirect Cost
Name
University of Kentucky
Department
Pharmacology
Type
Schools of Medicine
DUNS #
939017877
City
Lexington
State
KY
Country
United States
Zip Code
40526
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Memetimin, Hasiyet; Li, Dong; Tan, Kaiyuan et al. (2018) Myeloid Specific Deletion of Thrombospondin 1 Protects Against Inflammation and Insulin Resistance in Long-term Diet-induced Obese Male Mice. Am J Physiol Endocrinol Metab :
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Sui, Yipeng; Liu, Zun; Park, Se-Hyung et al. (2018) IKK? is a ?-catenin kinase that regulates mesenchymal stem cell differentiation. JCI Insight 3:
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Helsley, Robert N; Sui, Yipeng; Park, Se-Hyung et al. (2016) Targeting I?B kinase ? in Adipocyte Lineage Cells for Treatment of Obesity and Metabolic Dysfunctions. Stem Cells 34:1883-95
Park, Se-Hyung; Liu, Zun; Sui, Yipeng et al. (2016) IKK? Is Essential for Adipocyte Survival and Adaptive Adipose Remodeling in Obesity. Diabetes 65:1616-29