Journal
PLOS ONE
Volume 10, Issue 9, Pages -Publisher
PUBLIC LIBRARY SCIENCE
DOI: 10.1371/journal.pone.0138788
Keywords
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Categories
Funding
- National Natural Sciences Foundation of China [81300158, 81270269]
- Aid Program for Science and Technology Department of Human Province [2015JC3083]
- Outstanding Young Aid Program for Education Department of Human Province [13B103]
- Research and Innovation Aid Program for Graduate Student of Human Province [CX2014B393]
- Scientific Research Aid Program for Chinese Medicine of Human Province [201524]
- Aid Program for Science and Technology Bureau of HengYang City [2013KS20, 2013KS25]
- Aid Program for Science and Technology Innovative Research Team in Higher Educational Institutions of Hunan Province [2008-244]
- Construct Program of the Key Discipline in Hunan Province, Research and Innovation Aid Program for College Student of University of South China, China [52]
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Recent studies have suggested that miR-590 may play critical roles in cardiovascular disease. This study was designed to determine the effects of miR-590 on lipoprotein lipase (LPL) expression and development of atherosclerosis in apolipoprotein E knockout (apoE(-/-)) mice and explore the potential mechanisms. En face analysis of the whole aorta revealed that miR-590 significantly decreased aortic atherosclerotic plaque size and lipid content in apoE (-/-) mice. Double immunofluorescence staining in cross-sections of the proximal aorta showed that miR-590 agomir reduced CD68 and LPL expression in macrophages in atherosclerotic lesions. MiR-590 agomir down-regulated LPL mRNA and protein expression as analyzed by RT-qPCR and western blotting analyses, respectively. Consistently, miR-590 decreased the expression of CD36 and scavenger receptor A1 (SRA1) mRNA and protein. High-performance liquid chromatography (HPLC) analysis confirmed that treatment with miR-590 agomir reduced lipid levels either in plasma orinabdominal cavity macrophages of apoE(-/-) mice. ELISA analysis showed that miR-590 agomir decreased plasma levels of proinflammatory cytokines, such as tumor necrosis factor-alpha (TNF-alpha), monocyte chemotactic protein-1 (MCP-1), interleukin-1 beta (IL-1 beta) and interleukin-6 (IL-6). In contrast, treatment with miR-590 antagomir prevented or reversed these effects. Taken together, these results reveal a novel mechanism of miR-590 effects, and may provide new insights into the development of strategies for attenuating lipid accumulation and pro-inflammatory cytokine secretion.
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