Obesity, Metabolic Syndrome, and Type 2 diabetes are characterized by insulin resistance affecting multiple tissues (e.g., liver, muscle, and fat). Recent studies determined that intracellular autophagy plays an important role maintaining the metabolic health of tissues involved in the pathogenesis of insulin resistance. Autophagy is the intracellular lysosomal trafficking pathway that maintains energy homeostasis and counteracts multiple forms of cellular stress. In addition, autophagy is the sole mechanism for mitochondrial degradation and turnover in cells. Autophagy functions in skeletal muscle, liver, pancreatic beta cells, and hypothalamus to maintain insulin-glucose homeostasis;in addition, autophagy is required for lipolysis in liver. Prior studies examining the role of autophagy in adipose tissue utilized mouse models in which adipocyte autophagy was impaired during embryogenesis. These mice were lean and protected from diet-induced obesity, and exhibited enhanced insulin sensitivity and glucose intolerance. Such observations led to speculations that inhibiting autophagy in adipocytes might provide a promising strategy for treating or preventing obesity and its metabolic consequences. However, despite their apparently favorable metabolic phenotype, the mice with embryonic impairment of autophagy were not healthy: they exhibit increased rates of death (40% at 12 weeks of age) and inflammation and macrophage infiltration in adipose tissue. Due to the extreme alterations of adipocyte development and adipose tissue depot formation in these mice, they are not adequate models for assessing the post-developmental role of autophagy in the mature adipocyte. We hypothesize autophagy plays an important, protective function in mature adipocytes, and post-developmental impairment of adipocyte autophagy will induce intracellular stress and insulin-resistance via established signaling mechanisms;in addition, we predict """"""""autophagic stress"""""""" will cause release of unique circulating factors from adipocytes that drive systemic insulin-resistance and glucose intolerance via direct effects on other organs (e.g., liver, muscle, and pancreatic beta cells). The Overall Objectives of this project are: (i) to determine the role of adipocyte autophagy in the pathogenesis of insulin-resistance and glucose intolerance in vivo by defining specific target tissues and molecular actions through which adipocyte autophagy regulates systemic metabolism in the adult;and (ii) to define the normal regulation and metabolic functions of autophagy in mature adipocytes, independently of the role of autophagy in adipocyte development/differentiation. We genetically engineered mice so that autophagy can be turned off in adulthood, after the developmental period of intense adipogenesis, via a tamoxifen- inducible genetic impairment. Preliminary findings with """"""""mature adipocyte autophagy knockout mice"""""""" indicate autophagy does not regulate adiposity but is necessary for healthy insulin-glucose homeostasis. In the proposed work we will extend these observations to a systematic assessment of the tissue specific-mechanisms through which impairment of autophagy in mature adipocytes causes insulin resistance and glucose intolerance in mice in vivo (Aim #1);and we will make use of cultured primary adipocyte progenitor cells to study how the timing of autophagy impairment during adipogenesis influences the metabolic phenotype of adipocytes in vitro (Aim #2).

Public Health Relevance

Autophagy is a key metabolic process within cells that is regulated by nutrients and insulin. Recent work has shown that autophagy is required in several tissues for maintaining normal responses to insulin and normal regulation of glucose. The proposed work will determine how autophagy regulates aspects of normal adipocyte biology and its role in several forms of adipocyte dysfunction that contribute to insulin resistance and glucose intolerance at the whole body level. Prior work in this area utilized animal models with developmental impairment of adipocyte development (adipogenesis). The propose work will be the first to assess the post- developmental role of autophagy in normal adipocytes of adult mice. Understanding the role of autophagy in adipocyte biology may provide new strategies for the treatment or prevention of insulin resistance and Type 2 diabetes.

National Institute of Health (NIH)
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Research Project (R01)
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Integrative Physiology of Obesity and Diabetes Study Section (IPOD)
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Haft, Carol R
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University of Utah
Internal Medicine/Medicine
Schools of Medicine
Salt Lake City
United States
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Cai, Jinjin; Pires, Karla M; Ferhat, Maroua et al. (2018) Autophagy Ablation in Adipocytes Induces Insulin Resistance and Reveals Roles for Lipid Peroxide and Nrf2 Signaling in Adipose-Liver Crosstalk. Cell Rep 25:1708-1717.e5
Thompson, Spencer J; Sargsyan, Ashot; Lee, Seung-Ah et al. (2017) Hepatocytes Are the Principal Source of Circulating RBP4 in Mice. Diabetes 66:58-63
Sargsyan, A; Cai, J; Fandino, L B et al. (2015) Rapid parallel measurements of macroautophagy and mitophagy in mammalian cells using a single fluorescent biosensor. Sci Rep 5:12397
Bharath, Leena P; Mueller, Robert; Li, Youyou et al. (2014) Impairment of autophagy in endothelial cells prevents shear-stress-induced increases in nitric oxide bioavailability. Can J Physiol Pharmacol 92:605-12
Boudina, Sihem; Graham, Timothy E (2014) Mitochondrial function/dysfunction in white adipose tissue. Exp Physiol 99:1168-78