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<ns5:p><ns5:bold>Background:</ns5:bold> The K<ns5:sub>ATP</ns5:sub> channel plays a key role in glucose homeostasis by coupling metabolically generated changes in ATP to insulin secretion from pancreatic beta-cells.  Gain-of-function mutations in either the pore-forming (Kir6.2) or regulatory (SUR1) subunit of this channel are a common cause of transient neonatal diabetes mellitus (TNDM), in which diabetes presents shortly after birth but remits within the first few years of life, only to return in later life. The reasons behind this time dependence are unclear.</ns5:p><ns5:p> <ns5:bold>Methods:</ns5:bold> In an attempt to understand the mechanism behind diabetes remission and relapse, we generated mice expressing the common TNDM mutation SUR1-R1183W. We employed Cre/LoxP technology for both inducible and constitutive expression of SUR1-R1183W specifically in mouse beta-cells, followed by investigation of their phenotype using glucose tolerance tests and insulin secretion from isolated islets. </ns5:p><ns5:p> <ns5:bold>Results:</ns5:bold> We found that the R1183W mutation impaired inhibition of K<ns5:sub>ATP</ns5:sub> channels by ATP when heterologously expressed in human embryonic kidney cells. However, neither induced nor constitutive expression of SUR1-R1183W in mice resulted in changes in blood glucose homeostasis, compared to littermate controls. When challenged with a high fat diet, female mice expressing SUR1-R1183W showed increased weight gain, elevated blood glucose and impaired glycaemic control, but glucose-stimulated insulin secretion from pancreatic islets appeared unchanged.</ns5:p><ns5:p> <ns5:bold>Conclusions:</ns5:bold> The mouse model of TNDM did not recapitulate the human phenotype. We discuss multiple potential reasons why this might be the case. Based on our findings, we recommend future TNDM mouse models employing a gain-of-function SUR1 mutation should be created using the minimally invasive CRISPR/Cas technology, which avoids many potential pitfalls associated with the Cre/LoxP system.</ns5:p>

Original publication

DOI

10.12688/wellcomeopenres.15529.1

Type

Journal article

Journal

Wellcome Open Research

Publisher

Faculty of 1000 Ltd

Publication Date

30/01/2020

Volume

5

Pages

15 - 15