TY - JOUR
T1 - Tau suppresses microtubule-regulated pancreatic insulin secretion
AU - Mangiafico, Salvatore P.
AU - Tuo, Qing Zhang
AU - Li, Xiao Lan
AU - Liu, Yu
AU - Haralambous, Christian
AU - Ding, Xu Long
AU - Ayton, Scott
AU - Wang, Qing
AU - Laybutt, D. Ross
AU - Chan, Jeng Yie
AU - Zhang, Xiang
AU - Kos, Cameron
AU - Thomas, Helen E.
AU - Loudovaris, Thomas
AU - Yang, Chieh Hsin
AU - Joannides, Christos N.
AU - Lamont, Benjamin J.
AU - Dai, Lunzhi
AU - He, Hai Huai
AU - Dong, Biao
AU - Andrikopoulos, Sofianos
AU - Bush, Ashley I.
AU - Lei, Peng
N1 - Publisher Copyright:
© 2023, The Author(s), under exclusive licence to Springer Nature Limited.
PY - 2023/9
Y1 - 2023/9
N2 - Tau protein is implicated in the pathogenesis of Alzheimer’s disease (AD) and other tauopathies, but its physiological function is in debate. Mostly explored in the brain, tau is also expressed in the pancreas. We further explored the mechanism of tau’s involvement in the regulation of glucose-stimulated insulin secretion (GSIS) in islet β-cells, and established a potential relationship between type 2 diabetes mellitus (T2DM) and AD. We demonstrate that pancreatic tau is crucial for insulin secretion regulation and glucose homeostasis. Tau levels were found to be elevated in β-islet cells of patients with T2DM, and loss of tau enhanced insulin secretion in cell lines, drosophila, and mice. Pharmacological or genetic suppression of tau in the db/db diabetic mouse model normalized glucose levels by promoting insulin secretion and was recapitulated by pharmacological inhibition of microtubule assembly. Clinical studies further showed that serum tau protein was positively correlated with blood glucose levels in healthy controls, which was lost in AD. These findings present tau as a common therapeutic target between AD and T2DM.
AB - Tau protein is implicated in the pathogenesis of Alzheimer’s disease (AD) and other tauopathies, but its physiological function is in debate. Mostly explored in the brain, tau is also expressed in the pancreas. We further explored the mechanism of tau’s involvement in the regulation of glucose-stimulated insulin secretion (GSIS) in islet β-cells, and established a potential relationship between type 2 diabetes mellitus (T2DM) and AD. We demonstrate that pancreatic tau is crucial for insulin secretion regulation and glucose homeostasis. Tau levels were found to be elevated in β-islet cells of patients with T2DM, and loss of tau enhanced insulin secretion in cell lines, drosophila, and mice. Pharmacological or genetic suppression of tau in the db/db diabetic mouse model normalized glucose levels by promoting insulin secretion and was recapitulated by pharmacological inhibition of microtubule assembly. Clinical studies further showed that serum tau protein was positively correlated with blood glucose levels in healthy controls, which was lost in AD. These findings present tau as a common therapeutic target between AD and T2DM.
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U2 - 10.1038/s41380-023-02267-w
DO - 10.1038/s41380-023-02267-w
M3 - Article
C2 - 37735502
AN - SCOPUS:85171638121
SN - 1359-4184
VL - 28
SP - 3982
EP - 3993
JO - Molecular Psychiatry
JF - Molecular Psychiatry
IS - 9
ER -