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Status |
Public on Mar 30, 2019 |
Title |
MicroRNA-223 ameliorates nonalcoholic steatohepatitis and cancer by targeting multiple inflammatory and oncogenic genes in hepatocytes |
Organism |
Mus musculus |
Experiment type |
Expression profiling by array
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Summary |
Here, we found that microRNA-223 (miR-223) was highly elevated in hepatocytes after high fat diet (HFD) feeding in mice and in human nonalcoholic steatohepatitis (NASH) samples. Genetic deletion of the miR-223 induced a full spectrum of nonalcoholic fatty liver disease (NAFLD) in mice after long-term (up to one year) HFD feeding including NASH-related steatosis, inflammation, fibrosis and HCC. To better explore the mechanisms underlying the abnormalities observed in HFD-fed miR-223KO mice, we examined hepatic gene expression in 3-month-HFD-fed WT and miR-223KO mice by microarray analysis. Finally, we revealed that miR-223 plays a key role in controlling steatosis-to-NASH progression by inhibiting hepatic Cxcl10 and Taz expression.
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Overall design |
Two-condition experiment, WT and miR-223KO.
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Contributor(s) |
He Y, Cai Y, Gao B |
Citation(s) |
30964207 |
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Submission date |
Mar 29, 2019 |
Last update date |
Jul 03, 2019 |
Contact name |
Yong He |
E-mail(s) |
yong.he.nih@gmail.com
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Phone |
3014807478
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Organization name |
NIAAA/NIH
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Street address |
5625 Fishers lane Room 2S-12
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City |
Rockville |
State/province |
MD |
ZIP/Postal code |
20852 |
Country |
USA |
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Platforms (1) |
GPL7202 |
Agilent-014868 Whole Mouse Genome Microarray 4x44K G4122F (Probe Name version) |
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Samples (8)
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Relations |
BioProject |
PRJNA529919 |