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• W2783808220 endingPage "3173" @default.
• W2783808220 startingPage "3166" @default.
• W2783808220 abstract "The microtubule-associated protein tau is highly expressed in pancreatic islets. Abnormally phosphorylated tau aggregates assemble into neurofibrillary tangles linked to Alzheimer's disease pathology and has also been found in islets of patients with type 2 diabetes. However, the significance of tau in islet function remains relatively unexplored. Therefore, we investigated the role of tau on β cell function and glucose homeostasis using tau knockout (tauKO) mice. TauKO mice were hyperglycemic and glucose intolerant at an early age. Islet insulin content was reduced and proinsulin levels were significantly elevated in tauKO mice, resulting in impaired glucose-stimulated insulin secretion. Loss of tau also resulted in increased epididymal fat mass and leptin levels, reduced glucose production, and insulin resistance at later ages, leading to complete onset of diabetes. Transgenic expression of human tau in islets was unable to rescue those defects in glucose regulation, indicating structural and/or functional differences between mouse and human tau. Cumulatively, these results suggest an important role for tau in the proper maintenance of pancreatic β cell function and glucose homeostasis.—Wijesekara, N., Gonçalves, R. A., Ahrens, R., De Felice, F. G., Fraser, P. E. Tau ablation in mice leads to pancreatic β cell dysfunction and glucose intolerance. FASEB J. 32, 3166–3173 (2018). www.fasebj.org" @default.
• W2783808220 created "2018-01-26" @default.
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• W2783808220 date "2018-01-18" @default.
• W2783808220 modified "2023-10-01" @default.
• W2783808220 title "Tau ablation in mice leads to pancreatic β cell dysfunction and glucose intolerance" @default.
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• W2783808220 doi "https://doi.org/10.1096/fj.201701352" @default.
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