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Glut4

KARATE: PKA-Induced KRAS4B-RHOA-mTORC2 Supercomplex Phosphorylates AKT in Insulin Signaling and Glucose Homeostasis

[Molecular Cell] By investigating insulin receptor signaling in human cells and biochemical reconstitution, scientists found that insulin induced the activation of mTORC2 toward AKT by assembling a supercomplex with KRAS4B and RHOA GTPases, termed KARATE (KRAS4B-RHOA-mTORC2 Ensemble).

A Xanthene Derivative, DS20060511, Attenuates Glucose Intolerance by Inducing Skeletal Muscle-Specific GLUT4 Translocation in Mice

[Communications Biology] Scientists showed a xanthene derivative, DS20060511, induced GLUT4 translocation to the skeletal muscle cell surface, thereby stimulating glucose uptake into the tissue.

The Promise(s) of Mesenchymal Stem Cell Therapy in Averting Preclinical Diabetes: Lessons from In Vivo and In Vitro Model Systems

[Scientific Reports] Investigators showed that intramuscular injection of placental (P)-MSCs homed more towards the visceral site, restored HOMA-IR and glucose homeostasis in the WNIN/GR-Ob rats. P-MSC therapy was effective in re-establishing the dysregulated cytokines.

Integrated Analysis of Long Non-Coding RNAs and mRNAs Associated with Malignant Transformation of Gastrointestinal Stromal Tumors

[Cell Death & Disease] The authors revealed a series of key pathways and hub long non-coding RNAs involved in the malignant transformation of gastrointestinal stromal tumors (GISTs). DNM3OS promoted GIST cell proliferation and mitosis by regulating the expression of GLUT4 and CD36.

Beta-Catenin Is Required for Optimal Exercise and Contraction Stimulated Skeletal Muscle Glucose Uptake

[Journal of Physiology] Muscle specific deletion of β-catenin induced in adult mice impaired both exercise and contraction (isolated muscle) induced glucose uptake without affecting running performance or canonical exercise signaling pathways.

Linking Metabolic Dysfunction with Cardiovascular Diseases: Brn-3b/POU4F2 Transcription Factor in Cardiometabolic Tissues in Health and Disease

[Cell Death & Disease] Scientists explore the emerging evidence that supports novel and important roles for the POU4F2/Brn-3b transcription factor in controlling cellular genes that regulate cardiometabolic function.

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