<?xml version="1.0" encoding="UTF-8"?><?xml-stylesheet type="text/xsl" href="static/style.xsl"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-04-29T03:58:54Z</responseDate><request verb="GetRecord" identifier="oai:riubu.ubu.es:10259/4994" metadataPrefix="qdc">https://riubu.ubu.es/oai/request</request><GetRecord><record><header><identifier>oai:riubu.ubu.es:10259/4994</identifier><datestamp>2021-11-10T09:38:26Z</datestamp><setSpec>com_10259_4725</setSpec><setSpec>com_10259_5086</setSpec><setSpec>com_10259_2604</setSpec><setSpec>col_10259_4726</setSpec></header><metadata><qdc:qualifieddc xmlns:qdc="http://dspace.org/qualifieddc/" xmlns:doc="http://www.lyncode.com/xoai" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:dcterms="http://purl.org/dc/terms/" xmlns:dc="http://purl.org/dc/elements/1.1/" xsi:schemaLocation="http://purl.org/dc/elements/1.1/ http://dublincore.org/schemas/xmls/qdc/2006/01/06/dc.xsd http://purl.org/dc/terms/ http://dublincore.org/schemas/xmls/qdc/2006/01/06/dcterms.xsd http://dspace.org/qualifieddc/ http://www.ukoln.ac.uk/metadata/dcmi/xmlschema/qualifieddc.xsd">
<dc:title>Insulin degrading enzyme is up-regulated in pancreatic β cells by insulin treatment</dc:title>
<dc:creator>Fernández Díaz, Cristina M. .</dc:creator>
<dc:creator>Escobar Curbelo, Luis .</dc:creator>
<dc:creator>López Acosta, J.F.</dc:creator>
<dc:creator>Lobatón, Carmen D.</dc:creator>
<dc:creator>Moreno, Alfredo</dc:creator>
<dc:creator>Sanz Ortega, Julián</dc:creator>
<dc:creator>Perdomo Hernández, Germán M.</dc:creator>
<dc:creator>Cózar Castellano, Irene</dc:creator>
<dc:subject>Insulin-degrading enzyme</dc:subject>
<dc:subject>Type 2 diabetes,</dc:subject>
<dc:subject>Insulin treatment,</dc:subject>
<dc:subject>OHAs</dc:subject>
<dc:subject>Beta-cells</dc:subject>
<dc:subject>Alpha-cells</dc:subject>
<dc:subject>Rodent islets</dc:subject>
<dc:subject>Human islets</dc:subject>
<dcterms:abstract>Insulin Degrading Enzyme (IDE) is an&#xd;
endopeptidase that degrades insulin and glucagon. Ide&#xd;
gene has been associated with type-2 diabetes mellitus&#xd;
(DM2). However, the physiological role(s) of IDE in&#xd;
glucose homeostasis and its potential therapeutic benefit&#xd;
remain not completely known.&#xd;
To contribute in the understanding of IDE's role in&#xd;
glucose metabolism, we analyzed IDE protein level in&#xd;
pancreatic islets from two hyperinsulinemic mouse&#xd;
models, db/db and high-fat diet (HFD) mice, as well as&#xd;
in human islets from DM2 patients treated with oral&#xd;
hypoglycemic agents (OHAs) or insulin. IDE protein&#xd;
level was detected by staining and by western-blot.&#xd;
INS1E cells, rat and human islets were treated with&#xd;
insulin and IDE protein level was studied.&#xd;
We have shown for the first time IDE staining in&#xd;
rodent and human tissue, using the proper negative&#xd;
control, IDE null mouse tissue. Our staining indicates&#xd;
that IDE is expressed in both beta- and alpha-cells, with&#xd;
higher expression in alpha-cells. Db/db and HFD mice&#xd;
islets showed increased IDE protein level. Interestingly,&#xd;
human islets from DM2 patients treated with OHAs&#xd;
showed decreased IDE protein level in beta-cells.&#xd;
Meanwhile, islets from insulin-treated DM2 patients&#xd;
showed augmented IDE protein level compared to&#xd;
OHAs patients, pointing to an upregulation of IDE&#xd;
protein level stimulated by insulin. These data correlate&#xd;
nicely with insulin-stimulated upregulation of IDE in&#xd;
cultured INS1E cells, as well as in rat and human islets.In conclusion, our study shows that IDE is expressed&#xd;
in pancreatic beta- and alpha-cells of both rodents and&#xd;
humans, having higher expression in alpha-cells.&#xd;
Furthermore, insulin stimulates IDE protein level in&#xd;
pancreatic beta-cells. These results may have&#xd;
implications in how DM2 patient’s treatment affects&#xd;
their beta-cell function.</dcterms:abstract>
<dcterms:dateAccepted>2018-11-02T10:09:38Z</dcterms:dateAccepted>
<dcterms:available>2018-11-02T10:09:38Z</dcterms:available>
<dcterms:created>2018-11-02T10:09:38Z</dcterms:created>
<dcterms:issued>2018-11</dcterms:issued>
<dc:type>info:eu-repo/semantics/article</dc:type>
<dc:identifier>0213-3911</dc:identifier>
<dc:identifier>http://hdl.handle.net/10259/4994</dc:identifier>
<dc:identifier>10.14670/HH-11-997</dc:identifier>
<dc:language>eng</dc:language>
<dc:relation>Histology and Histopathology. 2018, V. 33, n. 11, p. 1167-1180</dc:relation>
<dc:relation>http://www.hh.um.es/2018/HH_33_11_2018.htm</dc:relation>
<dc:relation>info:eu-repo/grantAgreement/MINECO/SAF2014-58702-C2-1-R</dc:relation>
<dc:relation>info:eu-repo/grantAgreement/MINECO/SAF2014-58702-C2-2-R</dc:relation>
<dc:rights>http://creativecommons.org/licenses/by-nc-nd/4.0/</dc:rights>
<dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
<dc:rights>Attribution-NonCommercial-NoDerivatives 4.0 International</dc:rights>
<dc:publisher>Universidad de Murcia</dc:publisher>
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