Insulin and glucose play a role in foam cell formation and function
- Pavel N. Shashkin(corresponding author),
- Nitin Jain,
- Yury I. Miller,
- Benjamin A. Rissing,
- Yuqing Huo,
- Susanna R. Keller
- University of Virginia,
- Cleveland Clinic Foundation,
- Pfizer,
- University of California at San Diego,
- University of Minnesota Twin Cities
Open access
Sustainable Development Goals
- SDG 3 Good Health and Well
Abstract
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® 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 I was significantly down-regulated. In hyperinsulinemic hyperglycemic conditions, modified LDL upregulated Akt phosphorylation and expression of the insulin-regulated aminopeptidase. The level of proinflammatory cytokines, IL-1β, 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.
Publication Information
Output type
Original language
English (US)Article number
13Journal (Volume, Issue Number)
Cardiovascular Diabetology (Volume 5)Publication milestones
- Published - 06/20/2006
Publication status
ISSN
1475-2840Publication IDs
- Scopus: 33747598913
- PubMed: 16787541
- ORCID: /0000-0002-0305-4122/work/124760183
