Reversal of hyperlipidemia with a genetic switch favorably affects the content and inflammatory state of macrophages in atherosclerotic plaques.

Abstract

BACKGROUND:

We previously showed that the progression of atherosclerosis in the Reversa mouse (Ldlr(-/-Apob100/100Mttpfl/fl) Mx1Cre(+/+)) was arrested when the hyperlipidemia was normalized by inactivating the gene for microsomal triglyceride transfer protein. Here, we tested whether atherosclerosis would regress if the lipid levels were reduced after advanced plaques formed.

METHODS AND RESULTS:

Reversa mice were fed an atherogenic diet for 16 weeks. Plasma lipid levels were then reduced. Within 2 weeks, this reduction led to decreased monocyte-derived (CD68(+)) cells in atherosclerotic plaques and was associated with emigration of these cells out of plaques. In addition, the fall in lipid levels was accompanied by lower plaque lipid content and by reduced expression in plaque CD68(+) cells of inflammatory genes and higher expression of genes for markers of antiinflammatory M2 macrophages. Plaque composition was affected more than plaque size, with the decreased content of lipid and CD68(+) cells balanced by a higher content of collagen. When the reduced lipid level was combined with the administration of pioglitazone to simulate the clinical aggressive lipid management and proliferator-activated receptor-γ agonist treatment, the rate of depletion of plaque CD68(+) cells was unaffected, but there was a further increase in their expression of antiinflammatory macrophage markers.

CONCLUSION:

The Reversa mouse is a new model of atherosclerosis regression. After lipid lowering, favorable changes in plaque composition were independent of changes in size. In addition, plaque CD68(+) cells became less inflammatory, an effect enhanced by treatment with pioglitazone.

• Authors: Jonathan E Feig, Sajesh Parathath, James X Rong, Stephanie L Mick, Yuliya Vengrenyuk, Lisa Grauer, Stephen G Young, Edward A Fisher
• Journal: Circulation (Circulation) Vol. 123 Issue 9 Pg. 989-98 (Mar 08 2011) ISSN: 1524-4539 [Electronic] United States
• PMID: 21339485 (Publication Type: Comparative Study, Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't)

Chemical References

• Carrier Proteins
• microsomal triglyceride transfer protein

Topics

• Animals
• Carrier Proteins (antagonists & inhibitors, genetics, metabolism)
• Cell Movement (genetics)
• Disease Models, Animal
• Gene Targeting (methods)
• Genes, Switch (genetics)
• Genetic Therapy (methods)
• Hypercholesterolemia (genetics, pathology, therapy)
• Inflammation (genetics, pathology, therapy)
• Macrophages (classification, pathology)
• Mice
• Mice, Knockout
• Mice, Transgenic
• Microsomes (metabolism)
• Monocytes (metabolism, pathology)
• Plaque, Atherosclerotic (genetics, pathology, therapy)