[HTML][HTML] Long noncoding RNA MALAT1 promotes hepatic steatosis and insulin resistance by increasing nuclear SREBP-1c protein stability

C Yan, J Chen, N Chen - Scientific reports, 2016 - nature.com
C Yan, J Chen, N Chen
Scientific reports, 2016nature.com
Metastasis-associated lung adenocarcinoma transcript 1 (MALAT1) is implicated in liver cell
proliferation. However, its role in hepatic steatosis and insulin resistance remain poorly
understood. The aim of this study was to investigate the effects of MALAT1 on hepatic lipid
accumulation and its potential targets. As expected, MALAT1 expression is increased in
hepatocytes exposed to palmitate and livers of ob/ob mice. Knockdown of MALAT1
expression dramatically suppressed palmitate-induced lipid accumulation and the increase …
Abstract
Metastasis-associated lung adenocarcinoma transcript 1 (MALAT1) is implicated in liver cell proliferation. However, its role in hepatic steatosis and insulin resistance remain poorly understood. The aim of this study was to investigate the effects of MALAT1 on hepatic lipid accumulation and its potential targets. As expected, MALAT1 expression is increased in hepatocytes exposed to palmitate and livers of ob/ob mice. Knockdown of MALAT1 expression dramatically suppressed palmitate-induced lipid accumulation and the increase of nuclear SREBP-1c protein in HepG2 cells. In addition, RNA immunoprecipitation and RNA pull-down assay confirmed that MALAT1 interacted with SREBP-1c to stabilize nuclear SREBP-1c protein. Finally, injection of si-MALAT1 prevented hepatic lipid accumulation and insulin resistance in ob/ob mice. In conclusion, our observations suggest that MALAT1 promotes hepatic steatosis and insulin resistance by increasing nuclear SREBP-1c protein stability.
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