The Adipose Tissue Core will provide a wide variety of cost-effective services for the study of? human and mouse adipose tissue. Services will include techniques of cell separation and sorting,? histology, molecular biology and protein chemistry. Specifically, freshly isolated human and mouse? fat samples will be subjected to collagenase digestion (under conditions least likely to alter gene? expression) to separate primary adipocytes from the stromal vascular fraction. Adipose tissue? macrophages will subsequently be separated from the stromal vascular fraction with antibodycoated? magnetic beads. Gene expression will be analyzed in whole adipose tissue and its cellular? components using quantitative 'real-time' reverse-transcriptase polymerase chain reaction (rt-PCR,? Roche LightCycler). Quantification of RNA copy number will be derived from plasmid standard? curves for every gene of interest. Analysis of gene expression will be complemented by analysis of? protein expression of key adipocyte secretory products by Western blotting. Additionally, Western? blotting will be used to study the activation of various components of the insulin signaling pathway? in adipose tissue sampled under a variety of in vivo conditions. Quantitative assessment of? macrophage infiltration into adipose tissue will be performed by two alternative methods:? quantitative rt-PCR (using specific macrophage markers) and Fluorescence Activated Cell Sorting? (FACS) analysis. Since many of the above techniques require freshly obtained adipose tissue, the? concentration of these techniques in one Core should favor efficiency and minimize handling.? The following are several additional, highly specialized techniques offered by the Core. Adipocyte? size and number will be quantified following osmium fixation of adipose tissue samples. Serial? biopsies of rat adipose tissue will be performed in vivo by Dr. Vasselli. Lipoprotein lipase activity will? be assayed in frozen adipose tissue samples by Dr. Johnson. Recombinant adipokine production? will be provided by Dr. Lawrence Shapiro.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Center Core Grants (P30)
Project #
5P30DK026687-27
Application #
7418671
Study Section
Special Emphasis Panel (ZDK1)
Project Start
2007-04-01
Project End
2011-03-31
Budget Start
2007-04-01
Budget End
2008-03-31
Support Year
27
Fiscal Year
2007
Total Cost
$128,293
Indirect Cost
Name
St. Luke's-Roosevelt Institute for Health Sciences
Department
Type
DUNS #
623216371
City
New York
State
NY
Country
United States
Zip Code
10019
Pizinger, Theresa; Kovtun, Kyle; RoyChoudhury, Arindam et al. (2018) Pilot study of sleep and meal timing effects, independent of sleep duration and food intake, on insulin sensitivity in healthy individuals. Sleep Health 4:33-39
Kissileff, H R; Herzog, M (2018) Progressive ratio (PR) schedules and the sipometer: Do they measure wanting, liking, and/or reward? A tribute to Anthony Sclafani and Karen Ackroff. Appetite 122:44-50
Pan, Xiaoyue; Schwartz, Gary J; Hussain, M Mahmood (2018) Oleoylethanolamide differentially regulates glycerolipid synthesis and lipoprotein secretion in intestine and liver. J Lipid Res 59:2349-2359
Davidson, Lance E; Yu, Wen; Goodpaster, Bret H et al. (2018) Fat-Free Mass and Skeletal Muscle Mass Five Years After Bariatric Surgery. Obesity (Silver Spring) 26:1130-1136
Millings, Elizabeth J; De Rosa, Maria Caterina; Fleet, Sarah et al. (2018) ILDR2 has a negligible role in hepatic steatosis. PLoS One 13:e0197548
Peaceman, Alan M; Clifton, Rebecca G; Phelan, Suzanne et al. (2018) Lifestyle Interventions Limit Gestational Weight Gain in Women with Overweight or Obesity: LIFE-Moms Prospective Meta-Analysis. Obesity (Silver Spring) 26:1396-1404
Espeland, Mark A; Luchsinger, Jose A; Neiberg, Rebecca H et al. (2018) Long Term Effect of Intensive Lifestyle Intervention on Cerebral Blood Flow. J Am Geriatr Soc 66:120-126
Liu, Shunmei; Marcelin, Genevieve; Blouet, Clemence et al. (2018) A gut-brain axis regulating glucose metabolism mediated by bile acids and competitive fibroblast growth factor actions at the hypothalamus. Mol Metab 8:37-50
Cheng, X; Zhang, Y; Wang, C et al. (2018) The optimal anatomic site for a single slice to estimate the total volume of visceral adipose tissue by using the quantitative computed tomography (QCT) in Chinese population. Eur J Clin Nutr 72:1567-1575
Fang, Hongjuan; Berg, Elizabeth; Cheng, Xiaoguang et al. (2018) How to best assess abdominal obesity. Curr Opin Clin Nutr Metab Care 21:360-365

Showing the most recent 10 out of 809 publications