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Expression data in mouse liver expressing or not the adapter Grb14

ABSTRACT: Grb14 is an endogenous inhibitor of insulin signaling We used microarrays to investigate gene expression patterns after Grb14 silencing in mouse liver

ORGANISM(S): Mus musculus

PROVIDER: GSE81387 | GEO | 2016/10/28

SECONDARY ACCESSION(S): PRJNA321424

REPOSITORIES: GEO

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Expression data in mouse liver expressing or not the adapter Grb14

Project description:Grb14 is an endogenous inhibitor of insulin signaling We used microarrays to investigate gene expression patterns after Grb14 silencing in mouse liver

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Expression data in mouse liver expressing or not the adapter Grb14

Project description:Grb14 is an endogenous inhibitor of insulin signaling We used microarrays to investigate gene expression patterns after Grb14 silencing in mouse liver Ten week old mice were injected intraveinously with recombinant adenovirus expressing a control sh RNA (sh scramble) or a sh targetting Grb14 (shGrb14), and liver were studied in the fed state 7 days after the infection

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Inhibition of Grb14, a negative modulator of insulin signaling, improves glucose homeostasis without causing cardiac dysfunction

Project description:Insulin resistance increases patient’s risk of developing type 2 diabetes (T2D), nonalcoholic steatohepatitis (NASH) and a host of other comorbidities including cardiovascular disease and cancer. At the molecular level, insulin exerts its function through the insulin receptor (IR), a transmembrane receptor tyrosine kinase. Data from human genetic studies have shown that Grb14 functions as a negative modulator of IR activity, and germline Grb14-knockout (KO) mice have improved insulin signaling in liver and muscle tissues. Here, we show that Grb14 knockdown in the liver and the heart with an AAV-shRNA (Grb14-shRNA) improves glucose homeostasis in diet-induced obese (DIO) mice. A previous report has shown that germline deletion of Grb14 in mice results in cardiac hypertrophy and decreased systolic function, effects that could severely limit the therapeutic potential of targeting Grb14. In this report, we demonstrate that there are no significant changes in hemodynamic function as measured by echocardiography in DIO Grb14 and DIO sham mice for a period of four months. While additional studies are needed to further establish efficacy and to de-risk potential negative cardiac effects in pre-clinical heart failure models, our data support inhibiting Grb14 to treat diabetes and related conditions.

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Project description:Liver macrophages inhibit the endogenous antioxidant response in obesity-associated insulin resistance [miRNA-Seq]

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Expression data from liver, muscle and fat tissue of children with end stage liver disease

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