Tau suppresses microtubule-regulated pancreatic insulin secretion
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-stimu...
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Veröffentlicht in: | Molecular psychiatry 2023-09, Vol.28 (9), p.3982-3993 |
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creator | Mangiafico, Salvatore P. Tuo, Qing-Zhang Li, Xiao-Lan Liu, Yu Haralambous, Christian Ding, Xu-Long Ayton, Scott Wang, Qing Laybutt, D. Ross Chan, Jeng Yie Zhang, Xiang Kos, Cameron Thomas, Helen E. Loudovaris, Thomas Yang, Chieh-Hsin Joannides, Christos N. Lamont, Benjamin J. Dai, Lunzhi He, Hai-Huai Dong, Biao Andrikopoulos, Sofianos Bush, Ashley I. Lei, Peng |
description | 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. |
doi_str_mv | 10.1038/s41380-023-02267-w |
format | Article |
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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.</description><identifier>ISSN: 1359-4184</identifier><identifier>EISSN: 1476-5578</identifier><identifier>DOI: 10.1038/s41380-023-02267-w</identifier><identifier>PMID: 37735502</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>13/1 ; 13/51 ; 14/34 ; 38/91 ; 631/337 ; 692/699 ; Alzheimer Disease - metabolism ; Alzheimer's disease ; Animals ; Behavioral Sciences ; Beta cells ; Biological Psychology ; Blood levels ; Cell lines ; Diabetes mellitus (non-insulin dependent) ; Diabetes Mellitus, Type 2 - metabolism ; Genetic suppression ; Glucose ; Glucose - metabolism ; Homeostasis ; Humans ; Insulin ; Insulin - metabolism ; Insulin Secretion ; Islet cells ; Medicine ; Medicine & Public Health ; Mice ; Neurodegenerative diseases ; Neurosciences ; Pancreas ; Pancreas - metabolism ; Pancreas - pathology ; Pharmacotherapy ; Psychiatry ; Secretion ; Tau protein ; tau Proteins - metabolism ; Therapeutic targets</subject><ispartof>Molecular psychiatry, 2023-09, Vol.28 (9), p.3982-3993</ispartof><rights>The Author(s), under exclusive licence to Springer Nature Limited 2023. Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.</rights><rights>2023. The Author(s), under exclusive licence to Springer Nature Limited.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c375t-c009340db6dc318cff892a794b0454edab33df9de1c14abc92257775954eaa823</citedby><cites>FETCH-LOGICAL-c375t-c009340db6dc318cff892a794b0454edab33df9de1c14abc92257775954eaa823</cites><orcidid>0000-0002-3003-8910 ; 0000-0001-9034-4154 ; 0000-0002-3479-2427 ; 0000-0001-5652-1962 ; 0000-0001-8259-9069 ; 0000-0002-6242-5990</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1038/s41380-023-02267-w$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1038/s41380-023-02267-w$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,780,784,27923,27924,41487,42556,51318</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/37735502$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Mangiafico, Salvatore P.</creatorcontrib><creatorcontrib>Tuo, Qing-Zhang</creatorcontrib><creatorcontrib>Li, Xiao-Lan</creatorcontrib><creatorcontrib>Liu, Yu</creatorcontrib><creatorcontrib>Haralambous, Christian</creatorcontrib><creatorcontrib>Ding, Xu-Long</creatorcontrib><creatorcontrib>Ayton, Scott</creatorcontrib><creatorcontrib>Wang, Qing</creatorcontrib><creatorcontrib>Laybutt, D. Ross</creatorcontrib><creatorcontrib>Chan, Jeng Yie</creatorcontrib><creatorcontrib>Zhang, Xiang</creatorcontrib><creatorcontrib>Kos, Cameron</creatorcontrib><creatorcontrib>Thomas, Helen E.</creatorcontrib><creatorcontrib>Loudovaris, Thomas</creatorcontrib><creatorcontrib>Yang, Chieh-Hsin</creatorcontrib><creatorcontrib>Joannides, Christos N.</creatorcontrib><creatorcontrib>Lamont, Benjamin J.</creatorcontrib><creatorcontrib>Dai, Lunzhi</creatorcontrib><creatorcontrib>He, Hai-Huai</creatorcontrib><creatorcontrib>Dong, Biao</creatorcontrib><creatorcontrib>Andrikopoulos, Sofianos</creatorcontrib><creatorcontrib>Bush, Ashley I.</creatorcontrib><creatorcontrib>Lei, Peng</creatorcontrib><title>Tau suppresses microtubule-regulated pancreatic insulin secretion</title><title>Molecular psychiatry</title><addtitle>Mol Psychiatry</addtitle><addtitle>Mol Psychiatry</addtitle><description>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.</description><subject>13/1</subject><subject>13/51</subject><subject>14/34</subject><subject>38/91</subject><subject>631/337</subject><subject>692/699</subject><subject>Alzheimer Disease - metabolism</subject><subject>Alzheimer's disease</subject><subject>Animals</subject><subject>Behavioral Sciences</subject><subject>Beta cells</subject><subject>Biological Psychology</subject><subject>Blood levels</subject><subject>Cell lines</subject><subject>Diabetes mellitus (non-insulin dependent)</subject><subject>Diabetes Mellitus, Type 2 - metabolism</subject><subject>Genetic suppression</subject><subject>Glucose</subject><subject>Glucose - metabolism</subject><subject>Homeostasis</subject><subject>Humans</subject><subject>Insulin</subject><subject>Insulin - metabolism</subject><subject>Insulin Secretion</subject><subject>Islet cells</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Mice</subject><subject>Neurodegenerative diseases</subject><subject>Neurosciences</subject><subject>Pancreas</subject><subject>Pancreas - metabolism</subject><subject>Pancreas - pathology</subject><subject>Pharmacotherapy</subject><subject>Psychiatry</subject><subject>Secretion</subject><subject>Tau protein</subject><subject>tau Proteins - metabolism</subject><subject>Therapeutic targets</subject><issn>1359-4184</issn><issn>1476-5578</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNp9kEtLAzEUhYMotlb_gAsZcOMmmuckWRbxBQU3dR0ymUyZMi-TCcV_b-pUBRcuwg053z039wBwidEtRlTeBYapRBARmg7JBdwdgTlmIoecC3mc7pQryLBkM3AWwhahvchPwYwKQTlHZA6WaxOzEIfBuxBcyNra-n6MRWwc9G4TGzO6MhtMZ70zY22zuguxqbssuPQy1n13Dk4q0wR3cagL8Pb4sL5_hqvXp5f75QpaKvgILUKKMlQWeWkplraqpCJGKFYgxpkrTUFpWanSYYuZKawihAshuEqiMZLQBbiZfAffv0cXRt3WwbqmMZ3rY9BE5hITzDFL6PUfdNtH36XfaaIQFZQyphJFJiptHIJ3lR583Rr_oTHS-4D1FLBOAeuvgPUuNV0drGPRuvKn5TvRBNAJCEnqNs7_zv7H9hMDOYbP</recordid><startdate>20230901</startdate><enddate>20230901</enddate><creator>Mangiafico, Salvatore P.</creator><creator>Tuo, Qing-Zhang</creator><creator>Li, Xiao-Lan</creator><creator>Liu, Yu</creator><creator>Haralambous, Christian</creator><creator>Ding, Xu-Long</creator><creator>Ayton, Scott</creator><creator>Wang, Qing</creator><creator>Laybutt, D. 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Ross</au><au>Chan, Jeng Yie</au><au>Zhang, Xiang</au><au>Kos, Cameron</au><au>Thomas, Helen E.</au><au>Loudovaris, Thomas</au><au>Yang, Chieh-Hsin</au><au>Joannides, Christos N.</au><au>Lamont, Benjamin J.</au><au>Dai, Lunzhi</au><au>He, Hai-Huai</au><au>Dong, Biao</au><au>Andrikopoulos, Sofianos</au><au>Bush, Ashley I.</au><au>Lei, Peng</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Tau suppresses microtubule-regulated pancreatic insulin secretion</atitle><jtitle>Molecular psychiatry</jtitle><stitle>Mol Psychiatry</stitle><addtitle>Mol Psychiatry</addtitle><date>2023-09-01</date><risdate>2023</risdate><volume>28</volume><issue>9</issue><spage>3982</spage><epage>3993</epage><pages>3982-3993</pages><issn>1359-4184</issn><eissn>1476-5578</eissn><abstract>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.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>37735502</pmid><doi>10.1038/s41380-023-02267-w</doi><tpages>12</tpages><orcidid>https://orcid.org/0000-0002-3003-8910</orcidid><orcidid>https://orcid.org/0000-0001-9034-4154</orcidid><orcidid>https://orcid.org/0000-0002-3479-2427</orcidid><orcidid>https://orcid.org/0000-0001-5652-1962</orcidid><orcidid>https://orcid.org/0000-0001-8259-9069</orcidid><orcidid>https://orcid.org/0000-0002-6242-5990</orcidid></addata></record> |
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subjects | 13/1 13/51 14/34 38/91 631/337 692/699 Alzheimer Disease - metabolism Alzheimer's disease Animals Behavioral Sciences Beta cells Biological Psychology Blood levels Cell lines Diabetes mellitus (non-insulin dependent) Diabetes Mellitus, Type 2 - metabolism Genetic suppression Glucose Glucose - metabolism Homeostasis Humans Insulin Insulin - metabolism Insulin Secretion Islet cells Medicine Medicine & Public Health Mice Neurodegenerative diseases Neurosciences Pancreas Pancreas - metabolism Pancreas - pathology Pharmacotherapy Psychiatry Secretion Tau protein tau Proteins - metabolism Therapeutic targets |
title | Tau suppresses microtubule-regulated pancreatic insulin secretion |
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