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Tau Suppresses Microtubule-Regulated Pancreatic Insulin Secretion

[Molecular Psychiatry] Scientists demonstrated that pancreatic tau was crucial for insulin secretion regulation and glucose homeostasis. Tau levels were found to be elevated in β-islet cells of patients with type 2 diabetes mellitus, and loss of tau enhanced insulin secretion in cell lines.

Hollow Microfiber Assembly-Based Endocrine Pancreas-on-a-Chip for Sugar Substitute Evaluation

[Advanced Healthcare Materials] The authors developed a new type of endocrine pancreas-on-a-chip based on a microfiber assembly and evaluated its stimulation of pancreatic secretion by glucose or sugar substitutes.

Deletion of Ascl1 in Pancreatic β-Cells Improves Insulin Secretion, Promotes Parasympathetic Innervation, and Attenuates Dedifferentiation during Metabolic Stress

[Molecular Metabolism] To determine the role of Achaete-scute homolog 1 (Ascl1) in metabolic-stress induced β-cell failure, researchers generated pancreatic β-cell-specific Ascl1 knockout mice and assessed β-cell function and gene expression in response to a normal diet, metabolic stress, and excitotoxic stress.

Activation of AMPK Ameliorates Acute Severe Pancreatitis by Suppressing Pancreatic Acinar Cell Necroptosis in Obese Mice Models

[Cell Death Discovery] Researchers selected C57BL/6 mice as lean mice models, ob/ob mice or diet induced obese mice as obese mice models and then induced experimental acute pancreatitis in mice via injections of caerulein.

Estimating Residual Undifferentiated Cells in Human Chemically Induced Pluripotent Stem Cell Derived Islets Using lncRNA as Biomarkers

[Scientific Reports] Scientists developed a highly sensitive assay to detect residual undifferentiated cells in islet cells derived from human chemically induced pluripotent stem cells, which were transgene-free and safer.

Direct Regulation of FNIP1 and FNIP2 by MEF2 Sustains MTORC1 Activation and Tumor Progression in Pancreatic Cancer

[Autophagy] The authors demonstrated that transcription factors myocyte enhancer factor 2A (MEF2A) and MEF2D synergistically regulated mechanistic target of rapamycin kinase complex 1 (MTORC1) activation via modulating its cyto-lysosome shutting.

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