Overexpression of complement component C5a accelerates the development of atherosclerosis in ApoE-knockout mice.

Abstract

BACKGROUND:

In this study, we investigated the direct effect of C5a overexpression on atherosclerosis.

METHODS AND RESULTS:

A recombinant adenovirus expressing mouse C5a (Ad-C5a) was constructed and injected intravenously into ApoE-/- mice. After 12 weeks of a high-fat diet, Ad-C5a injection produced more extensive lesions than control adenovirus, and its proathrosclerotic role was significantly blocked by C5a receptor antagonist. Immunohistochemical analysis showed enhanced macrophage infiltration in atherosclerotic regions with C5a overexpression. Trans-well assay revealed C5a receptor-dependent chemotaxis of C5a to macrophages. Furthermore, Ad-C5a overexpression promoted foam cell formation and lipid deposition but reduced collagen content. In addition, with Ad-C5a overexpression, the serum levels of interleukin 6 and tumor necrosis factor α were upregulated.

CONCLUSIONS:

C5a overexpression could accelerate the development of atherosclerosis in ApoE-/- mice by promoting macrophage recruitment, foam cell formation and inflammatory activation. Furthermore, its proatherogetic role is mediated by the C5a receptor.

• Authors: Guipeng An, Bo Li, Xiaoman Liu, Mingxiang Zhang, Fei Gao, Yuxia Zhao, Fengshuang An, Yun Zhang, Cheng Zhang
• Journal: Oncotarget (Oncotarget) Vol. 7 Issue 35 Pg. 56060-56070 (Aug 30 2016) ISSN: 1949-2553 [Electronic] United States
• PMID: 27517153 (Publication Type: Journal Article)

Chemical References

• AcPhe(ornithine-Pro-cyclohexylamine-Trp-Arg)
• Interleukin-6
• Peptides, Cyclic
• Receptor, Anaphylatoxin C5a
• Recombinant Proteins
• Tumor Necrosis Factor-alpha
• interleukin-6, mouse
• Complement C5a

Topics

• Adenoviridae (genetics)
• Animals
• Aorta (pathology)
• Atherosclerosis (blood, etiology, pathology)
• Chemotaxis
• Complement C5a (genetics, metabolism)
• Diet, High-Fat (adverse effects)
• Genetic Vectors (chemistry)
• HEK293 Cells
• Humans
• Interleukin-6 (blood)
• Macrophages (pathology)
• Male
• Mice
• Mice, Inbred C57BL
• Mice, Knockout, ApoE
• Peptides, Cyclic (pharmacology)
• RAW 264.7 Cells
• Receptor, Anaphylatoxin C5a (antagonists & inhibitors)
• Recombinant Proteins (genetics, metabolism)
• Transfection
• Tumor Necrosis Factor-alpha (blood)
• Up-Regulation