Tag results:

obesity

Roles of IκB Kinases and TANK-Binding Kinase 1 in Hepatic Lipid Metabolism and Nonalcoholic Fatty Liver Disease

[Experimental and Molecular Medicine] The authors review the biochemical steps of hepatic lipid metabolism, dysregulated lipid metabolism in obesity and nonalcoholic fatty liver disease (NAFLD), and the roles of IκB kinase complexes and TANK-binding kinase 1 in obesity and NAFLD.

CRISPR-Enhanced Human Adipocyte Browning as Cell Therapy for Metabolic Disease

[Nature Communications] Scientists applied methods to greatly expand human adipocyte progenitors from small samples of human subcutaneous adipose tissue and then disrupt the thermogenic suppressor gene NRIP1 by CRISPR.

The Hepatic Stellate Cells (HSTCs) and Adipose-Derived Mesenchymal Stem Cells (ASCs) Axis as a Potential Major Driver of Metabolic Syndrome – Novel Concept and...

[Stem Cell Reviews and Reports] Researchers suggested that inter-organ communication on the level of stem progenitor cells-HSTCs and ASCs could represents a key mechanism involved in controlling glucose tolerance as well as insulin sensitivity.

Targeting p21Cip1 Highly Expressing Cells in Adipose Tissue Alleviates Insulin Resistance in Obesity

[Cell Metabolism] Using single-cell transcriptomics, the authors identified a small, critically important, but previously unexamined cell population, p21Cip1 highly expressing (p21high) cells, which accumulated in adipose tissue with obesity.

Adipocyte-Derived Exosomes May Promote Breast Cancer Progression in Type 2 Diabetes

[Science Signaling] Researchers found that primary human adipocytes shed extracellular vesicles, specifically exosomes, that induced the expression of genes associated with epithelial-to-mesenchymal transition and cancer stem–like cell traits in cocultured breast cancer cell lines.

GRP75 Regulates Mitochondrial-Supercomplex Turnover to Modulate Insulin Sensitivity

[Diabetes] Scientists assessed the roles of GRP75, other than as a component, in insulin action in both in vitro and in vivo models with insulin resistance.

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