Regulatory B Cell–Specific Interleukin-10 Is Dispensable for Atherosclerosis Development in Mice. Issue 8 (August 2015)

• Record Type: Journal Article
• Authors: Sage, Andrew P.; Nus, Meritxell; Baker, Lauren L.; Finigan, Alison J.; Masters, Leanne M.; Mallat, Ziad
• Is Part Of: Arteriosclerosis, thrombosis, and vascular biology. Volume 35:Issue 8(2015)
• Publication Date: 2015-08
• Subjects: atherosclerosis -- interleukins -- lymphocytes; Arteriosclerosis -- Periodicals; Thrombosis -- Periodicals; Blood-vessels -- Pathophysiology -- Periodicals; Electronic journals; 616.13
• DOI: 10.1161/ATVBAHA.115.305568
• Languages: English
• ISSNs: 1079-5642

Abstract

Abstract : Objective—: To determine the role of regulatory B cell–derived interleukin (IL)-10 in atherosclerosis. Approach and Results—: We created chimeric Ldlr −/− mice with a B cell–specific deficiency in IL-10, and confirmed that purified B cells stimulated with lipopolysaccharide failed to produce IL-10 compared with control Ldlr −/− chimeras. Mice lacking B-cell IL-10 demonstrated enhanced splenic B-cell numbers but no major differences in B-cell subsets, T cell or monocyte distribution, and unchanged body weights or serum cholesterol levels compared with control mice. After 8 weeks on high-fat diet, there were no differences in aortic root or aortic arch atherosclerosis. In addition to plaque size, plaque composition (macrophages, T cells, smooth muscle cells, and collagen) was similar between groups. Conclusions—: In contrast to its prominent regulatory role in many immune-mediated diseases and its proposed modulatory role in atherosclerosis, B cell–derived IL-10 does not alter atherosclerosis in mice. Abstract : Supplemental Digital Content is available in the text.