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A newly identified microRNA, mmu-miR-7578, functions as a negative regulator on inflammatory cytokines tumor necrosis factor-? and interleukin-6 via targeting Egr1 in vivo.


ABSTRACT: Appropriate innate immune responses are required to protect an organism against foreign pathogens, and the immune response must be tightly controlled. Here, we report a new microRNA (miRNA) identified from a small RNA library from the epididymis, termed miR-7578, that acts as a negative regulator of inflammatory responses. It was abundantly expressed in immune-related organs and induced by lipopolysaccharide in the lung and epididymis, as well as macrophages stimulated with diverse Toll-like receptor ligands, in an NF-?B-dependent manner. mmu-miR-7578 inhibited the release of pro-inflammatory cytokines, including TNF? and IL6, by regulating its target gene Egr1, which encodes a transcription factor that activates TNF? and NF-?B expression. Transgenic mice overexpressing mmu-miR-7578 displayed higher resistance to endotoxin shock and lower plasma levels of TNF? and IL6, indicating that this miRNA acted as a negative molecule of immune response. In sum, we report a previously uncharacterized LPS-responsive miRNA that controls inflammatory response in a feedback loop by fine-tuning a key transcription factor in vivo.

SUBMITTER: Zhang J 

PROVIDER: S-EPMC3567682 | biostudies-literature | 2013 Feb

REPOSITORIES: biostudies-literature

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A newly identified microRNA, mmu-miR-7578, functions as a negative regulator on inflammatory cytokines tumor necrosis factor-α and interleukin-6 via targeting Egr1 in vivo.

Zhang Jinsong J   Xie Shengsong S   Ma Wubin W   Teng Yu Y   Tian Ye Y   Huang Xingxu X   Zhang Yonglian Y  

The Journal of biological chemistry 20121126 6


Appropriate innate immune responses are required to protect an organism against foreign pathogens, and the immune response must be tightly controlled. Here, we report a new microRNA (miRNA) identified from a small RNA library from the epididymis, termed miR-7578, that acts as a negative regulator of inflammatory responses. It was abundantly expressed in immune-related organs and induced by lipopolysaccharide in the lung and epididymis, as well as macrophages stimulated with diverse Toll-like rec  ...[more]

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