Insulin and glucose play a role in foam cell formation and function

被引:24
作者
Shashkin, Pavel N. [1 ,2 ]
Jain, Nitin [1 ,3 ]
Miller, Yury I. [4 ]
Rissing, Benjamin A. [1 ]
Huo, Yuqing [1 ,5 ]
Keller, Susanna R. [6 ]
Vandenhoff, George E. [6 ]
Nadler, Jerry L. [6 ]
McIntyre, Thomas M. [2 ]
机构
[1] Univ Virginia, Cardiovasc Res Ctr, Charlottesville, VA 22903 USA
[2] Cleveland Clin, Dept Cell Biol, Cleveland, OH 44195 USA
[3] Pfizer Inc, Groton, CT 06340 USA
[4] Univ Calif San Diego, Dept Med, La Jolla, CA 92093 USA
[5] Univ Minnesota, Dept Med, Minneapolis, MN 55455 USA
[6] Univ Virginia, Dept Internal Med, Div Endocrinol, Charlottesville, VA 22908 USA
关键词
Insulin Receptor; Insulin Signaling; Affymetrix GeneChip; Foam Cell Formation; Insulin Signaling Cascade;
D O I
10.1186/1475-2840-5-13
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Foam cell formation in diabetic patients often occurs in the presence of high insulin and glucose levels. To test whether hyperinsulinemic hyperglycemic conditions affect foam cell differentiation, we examined gene expression, cytokine production, and Akt phosphorylation in human monocyte-derived macrophages incubated with two types of oxidized low density lipoprotein (LDL), minimally modified LDL (mmLDL) and extensively oxidized LDL (OxLDL). Methods and results: Using Affymetrix GeneChip (R) arrays, we found that several genes directly related to insulin signaling were changed. The insulin receptor and glucose-6-phosphate dehydrogenase were upregulated by mmLDL and OxLDL, whereas insulin-induced gene 1 was significantly downregulated. In hyperinsulinemic hyperglycemic conditions, modified LDL upregulated Akt phosphorylation and expression of the insulin-regulated aminopeptidase. The level of proinflammatory cytokines, IL-l beta, IL-12, and IL-6, and of a 5-lipoxygenase eicosanoid, 5-hydroxyeicosatetraenoic acid (5-HETE), was also increased. Conclusion: These results suggest that the exposure of macrophages to modified low density lipoproteins in hyperglycemic hyperinsulinemic conditions affects insulin signaling and promotes the release of proinflammatory stimuli, such as cytokines and eicosanoids. These in turn may contribute to the development of insulin resistance.
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页数:11
相关论文
共 62 条
[1]  
Artie AD, 2004, J CLIN INVEST, V113, P1112
[2]  
Bey EA, 2000, J LIPID RES, V41, P489
[3]   Modulation of atherogenesis by chemokines [J].
Boisvert, WA .
TRENDS IN CARDIOVASCULAR MEDICINE, 2004, 14 (04) :161-165
[4]   INSULIN INSULIN-LIKE GROWTH FACTOR-I INDUCE ACTIN TRANSCRIPTION IN MOUSE FIBROBLASTS EXPRESSING CONSTITUTIVELY MYC GENE [J].
BUCHOU, T ;
GABEN, AM ;
PHANDINHTUY, F ;
MESTER, J .
MOLECULAR AND CELLULAR ENDOCRINOLOGY, 1991, 75 (03) :181-187
[5]  
Candido Riccardo, 2003, Curr Opin Investig Drugs, V4, P1088
[6]   p110 delta, a novel phosphatidylinositol 3-kinase catalytic subunit that associates with p85 and is expressed predominantly in leukocytes [J].
Chantry, D ;
Vojtek, A ;
Kashishian, A ;
Holtzman, DA ;
Wood, C ;
Gray, PW ;
Cooper, JA ;
Hoekstra, MF .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (31) :19236-19241
[7]  
CLINTON SK, 1992, AM J PATHOL, V140, P301
[8]   Inflammation: the link between insulin resistance, obesity and diabetes [J].
Dandona, P ;
Aljada, A ;
Bandyopadhyay, A .
TRENDS IN IMMUNOLOGY, 2004, 25 (01) :4-7
[9]   INSULIN-STIMULATED GLUCOSE-TRANSPORT IN CIRCULATING MONONUCLEAR-CELLS FROM NONDIABETIC AND IDDM SUBJECTS [J].
DANEMAN, D ;
ZINMAN, B ;
ELLIOTT, ME ;
BILAN, PJ ;
KLIP, A .
DIABETES, 1992, 41 (02) :227-234
[10]   The role of interleukin-4 and interleukin-12 in the progression of atherosclerosis in apolipoprotein E-deficient mice [J].
Davenport, P ;
Tipping, PG .
AMERICAN JOURNAL OF PATHOLOGY, 2003, 163 (03) :1117-1125