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Mmu-miR-27a-5p-Dependent Upregulation of MCPIP1 Inhibits the Inflammatory Response in LPS-Induced RAW264.7 Macrophage Cells
by
Zhu, Huapei
, Cheng, Ying
, Jia, Xiaoxiao
, Xu, Kailian
, Pang, Feng
, Zhao, Tianjing
, Wang, Fengyang
, Guo, Shiyu
, Du, Li
, Shi, Qiaoyun
, Jiao, Hanwei
in
3' Untranslated Regions - genetics
/ Animals
/ Base Sequence
/ Binding sites
/ Biomedical research
/ Biotechnology
/ Cloning
/ Cytokines
/ E coli
/ Genetic aspects
/ Genetic engineering
/ Health aspects
/ Immune system
/ Inflammation
/ Inflammation - metabolism
/ Inflammation - pathology
/ Interleukins - secretion
/ Lipopolysaccharides
/ Lipopolysaccharides - pharmacology
/ Macrophages
/ Macrophages - drug effects
/ Macrophages - metabolism
/ Macrophages - pathology
/ Macrophages - secretion
/ Methods
/ Mice
/ MicroRNA
/ MicroRNAs - genetics
/ MicroRNAs - metabolism
/ Molecular Sequence Data
/ Mutation
/ R&D
/ RAW 264.7 Cells
/ Real-Time Polymerase Chain Reaction
/ Research & development
/ Ribonucleases - genetics
/ Ribonucleases - metabolism
/ RNA sequencing
/ RNA, Messenger - genetics
/ RNA, Messenger - metabolism
/ Rodents
/ Studies
/ Up-Regulation - drug effects
/ Up-Regulation - genetics
2015
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Mmu-miR-27a-5p-Dependent Upregulation of MCPIP1 Inhibits the Inflammatory Response in LPS-Induced RAW264.7 Macrophage Cells
by
Zhu, Huapei
, Cheng, Ying
, Jia, Xiaoxiao
, Xu, Kailian
, Pang, Feng
, Zhao, Tianjing
, Wang, Fengyang
, Guo, Shiyu
, Du, Li
, Shi, Qiaoyun
, Jiao, Hanwei
in
3' Untranslated Regions - genetics
/ Animals
/ Base Sequence
/ Binding sites
/ Biomedical research
/ Biotechnology
/ Cloning
/ Cytokines
/ E coli
/ Genetic aspects
/ Genetic engineering
/ Health aspects
/ Immune system
/ Inflammation
/ Inflammation - metabolism
/ Inflammation - pathology
/ Interleukins - secretion
/ Lipopolysaccharides
/ Lipopolysaccharides - pharmacology
/ Macrophages
/ Macrophages - drug effects
/ Macrophages - metabolism
/ Macrophages - pathology
/ Macrophages - secretion
/ Methods
/ Mice
/ MicroRNA
/ MicroRNAs - genetics
/ MicroRNAs - metabolism
/ Molecular Sequence Data
/ Mutation
/ R&D
/ RAW 264.7 Cells
/ Real-Time Polymerase Chain Reaction
/ Research & development
/ Ribonucleases - genetics
/ Ribonucleases - metabolism
/ RNA sequencing
/ RNA, Messenger - genetics
/ RNA, Messenger - metabolism
/ Rodents
/ Studies
/ Up-Regulation - drug effects
/ Up-Regulation - genetics
2015
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Mmu-miR-27a-5p-Dependent Upregulation of MCPIP1 Inhibits the Inflammatory Response in LPS-Induced RAW264.7 Macrophage Cells
by
Zhu, Huapei
, Cheng, Ying
, Jia, Xiaoxiao
, Xu, Kailian
, Pang, Feng
, Zhao, Tianjing
, Wang, Fengyang
, Guo, Shiyu
, Du, Li
, Shi, Qiaoyun
, Jiao, Hanwei
in
3' Untranslated Regions - genetics
/ Animals
/ Base Sequence
/ Binding sites
/ Biomedical research
/ Biotechnology
/ Cloning
/ Cytokines
/ E coli
/ Genetic aspects
/ Genetic engineering
/ Health aspects
/ Immune system
/ Inflammation
/ Inflammation - metabolism
/ Inflammation - pathology
/ Interleukins - secretion
/ Lipopolysaccharides
/ Lipopolysaccharides - pharmacology
/ Macrophages
/ Macrophages - drug effects
/ Macrophages - metabolism
/ Macrophages - pathology
/ Macrophages - secretion
/ Methods
/ Mice
/ MicroRNA
/ MicroRNAs - genetics
/ MicroRNAs - metabolism
/ Molecular Sequence Data
/ Mutation
/ R&D
/ RAW 264.7 Cells
/ Real-Time Polymerase Chain Reaction
/ Research & development
/ Ribonucleases - genetics
/ Ribonucleases - metabolism
/ RNA sequencing
/ RNA, Messenger - genetics
/ RNA, Messenger - metabolism
/ Rodents
/ Studies
/ Up-Regulation - drug effects
/ Up-Regulation - genetics
2015
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Mmu-miR-27a-5p-Dependent Upregulation of MCPIP1 Inhibits the Inflammatory Response in LPS-Induced RAW264.7 Macrophage Cells
Journal Article
Mmu-miR-27a-5p-Dependent Upregulation of MCPIP1 Inhibits the Inflammatory Response in LPS-Induced RAW264.7 Macrophage Cells
2015
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Overview
Lipopolysaccharide (LPS) stimulates macrophages to release proinflammatory cytokines. MicroRNAs (miRNAs) are short noncoding RNAs that are involved in inflammatory reaction. Our previously study identified the downregulated expression of mmu-miR-27a-5p in RAW267.4 cells treated with LPS. To dissect the mechanism that mmu-miR-27a-5p regulates target genes and affects proinflammatory cytokine secretion more clearly, based on previous bioinformatics prediction data, one of the potential target genes, MCPIP1 was observed to be upregulated with qRT-PCR and western blot. Luciferase reporter assays were performed to further confirm in silico prediction and determine that MCPIP1 is the target of mmu-miR-27-5p. The results suggested that mmu-miR-27a-5p directly targeted the 3′-UTR of MCPIP1 and the interaction between mmu-miR-27-5p and the 3′-UTR of MCPIP1 is sequence-specific. MCPIP1 overexpression decreased the secretion of IL-6, IL-1β, and IL-10 in macrophage cells stimulated with LPS. Our findings may provide the important information for the precise roles of mmu-miR-27a-5p in the macrophage inflammatory response to LPS stimulation in the future.
Publisher
Hindawi Publishing Corporation,John Wiley & Sons, Inc
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