Obesity, which is characterized by excess adipose tissue mass, is associated with metabolic abnormalities? and systemic inflammation. The mechanism(s) responsible for this relationship is not completely known but? likely involves the endocrine functions of adipose tissue. Adipose tissue produces a variety of bioactive? substances (i.e. adipokines) with central or peripheral actions that regulate food intake and energy? expenditure (1). In addition, plasma concentrations of some adipokines are associated with many features? of the Metabolic Syndrome, such as insulin resistance, type 2 diabetes mellitus, dyslipidemia, and coronary? artery disease (2). Accordingly, the number of investigators who are interested in the molecular biology? and cellular physiology of adipocytes and adipose tissue is increasing. To address this growing interest at? Washington University, we conducted a survey of our faculty regarding their interest and need for research? services involving adipose tissue. In response to this survey, we propose an Adipocyte Biology Core? (ABC), which is specifically tailored to meet the needs of CNRU investigators and faculty in basic? and clinical departments who wish to conduct nutrition- or obesity- related adipose tissue research.? These services do not overlap with those provided by other cores, and services for adipose tissue cell? sizing and macrophage content will be coordinated with the Histology Core of the Diabetes Research and? Training Center to maximize efficiency and cost-effectiveness. The study of adipose tissue biology requires? specific methods, equipment and expertise that are difficult to assemble by individual investigators and? present a barrier to those who are new to this field. Therefore, the overall objective of the ABC is to? provide CNRU researchers with access to the training, expertise, and facilities needed for? comprehensive study of adipose tissue.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Center Core Grants (P30)
Project #
2P30DK056341-06
Application #
7116102
Study Section
Special Emphasis Panel (ZDK1-GRB-4 (J1))
Project Start
2006-04-01
Project End
2011-03-31
Budget Start
2006-05-01
Budget End
2007-03-31
Support Year
6
Fiscal Year
2006
Total Cost
$111,871
Indirect Cost
Name
Washington University
Department
Type
DUNS #
068552207
City
Saint Louis
State
MO
Country
United States
Zip Code
63130
Riek, Amy E; Oh, Jisu; Darwech, Isra et al. (2018) Vitamin D3 supplementation decreases a unique circulating monocyte cholesterol pool in patients with type 2 diabetes. J Steroid Biochem Mol Biol 177:187-192
Bittel, Adam J; Bohnert, Kathryn L; Reeds, Dominic N et al. (2018) Reduced Muscle Strength in Barth Syndrome May Be Improved by Resistance Exercise Training: A Pilot Study. JIMD Rep :
Shepherd, Andrew J; Copits, Bryan A; Mickle, Aaron D et al. (2018) Angiotensin II Triggers Peripheral Macrophage-to-Sensory Neuron Redox Crosstalk to Elicit Pain. J Neurosci 38:7032-7057
Cifarelli, Vincenza; Abumrad, Nada A (2018) Intestinal CD36 and Other Key Proteins of Lipid Utilization: Role in Absorption and Gut Homeostasis. Compr Physiol 8:493-507
Smith, Gordon I; Commean, Paul K; Reeds, Dominic N et al. (2018) Effect of Protein Supplementation During Diet-Induced Weight Loss on Muscle Mass and Strength: A Randomized Controlled Study. Obesity (Silver Spring) 26:854-861
Perry, Justin S A; Russler-Germain, Emilie V; Zhou, You W et al. (2018) Transfer of Cell-Surface Antigens by Scavenger Receptor CD36 Promotes Thymic Regulatory T Cell Receptor Repertoire Development and Allo-tolerance. Immunity 48:1271
Turecamo, S E; Walji, T A; Broekelmann, T J et al. (2018) Contribution of metabolic disease to bone fragility in MAGP1-deficient mice. Matrix Biol 67:1-14
Samovski, Dmitri; Dhule, Pallavi; Pietka, Terri et al. (2018) Regulation of Insulin Receptor Pathway and Glucose Metabolism by CD36 Signaling. Diabetes 67:1272-1284
Porter, Lane C; Franczyk, Michael P; Pietka, Terri et al. (2018) NAD+-dependent deacetylase SIRT3 in adipocytes is dispensable for maintaining normal adipose tissue mitochondrial function and whole body metabolism. Am J Physiol Endocrinol Metab 315:E520-E530
Acevedo, María Belén; Eagon, J Christopher; Bartholow, Bruce D et al. (2018) Sleeve gastrectomy surgery: when 2 alcoholic drinks are converted to 4. Surg Obes Relat Dis 14:277-283

Showing the most recent 10 out of 1334 publications