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C-reactive protein functions as a negative regulator of macrophage activation induced by apoptotic DNA
Protein & Cell ; (12): 672-679, 2011.
Article in English | WPRIM (Western Pacific) | ID: wpr-757055
Responsible library: WPRO
ABSTRACT
C-reactive protein (CRP), an acute-phase protein with an ability to bind to nuclear antigen, has been reported to regulate cytokine secretion and modulate immune responses. We previously reported that activated syngeneic lymphocyte-derived apoptotic DNA (apopDNA) could induce macrophage activation and contribute to the initiation and progression of lupus nephritis. It is reasonable to hypothesize that CRP might regulate apopDNA-induced macrophage activation. Herein, CRP was shown to promote macrophage-mediated apopDNA uptake by binding to apopDNA (CRP/apopDNA complex). Notably, CRP/apopDNA treatment inhibited the production of inflammatory cytokines and chemokines by macrophages which could be induced by apopDNA alone. Further coculture and transwell studies revealed that CRP/apopDNA-induced macrophages prohibited apopDNA-induced macrophage activation in an IL-10 dependent manner. These results provide insight into the potential mechanism of CRP regulatory activity in macrophage activation induced by apopDNA in the context of lupus nephritis and other autoimmune diseases.
Subject(s)
Full text: Available Database: WPRIM (Western Pacific) Main subject: Pharmacology / Physiology / Protein Binding / Lupus Nephritis / C-Reactive Protein / DNA / Enzyme-Linked Immunosorbent Assay / Cell Line, Tumor / Real-Time Polymerase Chain Reaction / Lupus Erythematosus, Systemic Limits: Animals Language: English Journal: Protein & Cell Year: 2011 Document type: Article
Full text: Available Database: WPRIM (Western Pacific) Main subject: Pharmacology / Physiology / Protein Binding / Lupus Nephritis / C-Reactive Protein / DNA / Enzyme-Linked Immunosorbent Assay / Cell Line, Tumor / Real-Time Polymerase Chain Reaction / Lupus Erythematosus, Systemic Limits: Animals Language: English Journal: Protein & Cell Year: 2011 Document type: Article
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