This project proposes to investigate the potential role of diabetes on the interaction between lipoproteins and extracellular proteoglycans of the artery wall, alterations of which might account for the increased atherosclerosis risk typical of diabetes. Studies will be undertaken to determine whether alterations in either lipoproteins or proteoglycans that might occur in diabetes will modify their interaction in such a manner that would result in the increased retention of lipoproteins in the artery wall. Features common to IDDM and NIDDM such as lipoprotein oxidation, non- enzymatic glycation of proteins, altered matrix gene expression, and development of renal complications are hypothesized to alter lipoprotein- proteoglycan interaction. These interactions may also be affected by the presence and nature of intermediary molecules such as apo E and lipoprotein lipase (LPL). Lipoprotein-proteoglycan interactions will be evaluated by in vitro experiments, by studying lipoproteins from subjects with diabetes and renal complications, and proteoglycan from subjects and renal complications, and proteoglycans from arteries of subjects with diabetes. Project 2 is part of an integrated program aimed at providing further understanding of the mechanisms of accelerated macrovascular disease in diabetes. As such, it interacts with each of the four other projects in this Program Project.

Project Start
2000-12-01
Project End
2002-03-31
Budget Start
1998-10-01
Budget End
1999-09-30
Support Year
42
Fiscal Year
2002
Total Cost
$130,479
Indirect Cost
Name
University of Washington
Department
Type
DUNS #
135646524
City
Seattle
State
WA
Country
United States
Zip Code
98195
Hutchins, Patrick M; Heinecke, Jay W (2015) Cholesterol efflux capacity, macrophage reverse cholesterol transport and cardioprotective HDL. Curr Opin Lipidol 26:388-93
Vaisar, Tomáš; Tang, Chongren; Babenko, Ilona et al. (2015) Inflammatory remodeling of the HDL proteome impairs cholesterol efflux capacity. J Lipid Res 56:1519-30
Hutchins, Patrick M; Ronsein, Graziella E; Monette, Jeffrey S et al. (2014) Quantification of HDL particle concentration by calibrated ion mobility analysis. Clin Chem 60:1393-401
Purnell, Jonathan Q; Zinman, Bernard; Brunzell, John D et al. (2013) The effect of excess weight gain with intensive diabetes mellitus treatment on cardiovascular disease risk factors and atherosclerosis in type 1 diabetes mellitus: results from the Diabetes Control and Complications Trial/Epidemiology of Diabetes Interven Circulation 127:180-7
Umemoto, Tomio; Han, Chang Yeop; Mitra, Poulami et al. (2013) Apolipoprotein AI and high-density lipoprotein have anti-inflammatory effects on adipocytes via cholesterol transporters: ATP-binding cassette A-1, ATP-binding cassette G-1, and scavenger receptor B-1. Circ Res 112:1345-54
Liu, Yuhua; Tang, Chongren (2012) Regulation of ABCA1 functions by signaling pathways. Biochim Biophys Acta 1821:522-9
de Boer, Ian H; Sachs, Michael C; Cleary, Patricia A et al. (2012) Circulating vitamin D metabolites and kidney disease in type 1 diabetes. J Clin Endocrinol Metab 97:4780-8
Hoofnagle, Andrew N; Wu, Mingyuan; Gosmanova, Albina K et al. (2010) Low clusterin levels in high-density lipoprotein associate with insulin resistance, obesity, and dyslipoproteinemia. Arterioscler Thromb Vasc Biol 30:2528-34
Tang, Chongren; Kanter, Jenny E; Bornfeldt, Karin E et al. (2010) Diabetes reduces the cholesterol exporter ABCA1 in mouse macrophages and kidneys. J Lipid Res 51:1719-28
Vaisar, Tomás; Kassim, Sean Y; Gomez, Ivan G et al. (2009) MMP-9 sheds the beta2 integrin subunit (CD18) from macrophages. Mol Cell Proteomics 8:1044-60

Showing the most recent 10 out of 24 publications