Volume 4, Issue 1 694198 pp. 7-12
Article
Open Access

Ins1 Gene Up-Regulated in a β-Cell Line Derived from Ins2 Knockout Mice

Loïc Leroux

Loïc Leroux

Department of Genetics, Development and Molecular Pathology Institut Cochin, INSERM, CNRS Université René Descartes 24 rue du Faubourg Saint-Jacques Paris 75014, France , univ-paris5.fr

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Béatrice Durel

Béatrice Durel

Department of Genetics, Development and Molecular Pathology Institut Cochin, INSERM, CNRS Université René Descartes 24 rue du Faubourg Saint-Jacques Paris 75014, France , univ-paris5.fr

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Valérie Autier

Valérie Autier

MERCK Laboratories Chilly Mazarin, France , merck.com

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Louise Deltour

Louise Deltour

Department of Genetics, Development and Molecular Pathology Institut Cochin, INSERM, CNRS Université René Descartes 24 rue du Faubourg Saint-Jacques Paris 75014, France , univ-paris5.fr

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Danielle Bucchini

Danielle Bucchini

Department of Genetics, Development and Molecular Pathology Institut Cochin, INSERM, CNRS Université René Descartes 24 rue du Faubourg Saint-Jacques Paris 75014, France , univ-paris5.fr

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Jacques Jami

Jacques Jami

Department of Genetics, Development and Molecular Pathology Institut Cochin, INSERM, CNRS Université René Descartes 24 rue du Faubourg Saint-Jacques Paris 75014, France , univ-paris5.fr

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Rajiv L. Joshi

Corresponding Author

Rajiv L. Joshi

Department of Genetics, Development and Molecular Pathology Institut Cochin, INSERM, CNRS Université René Descartes 24 rue du Faubourg Saint-Jacques Paris 75014, France , univ-paris5.fr

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First published: 20 November 2002
Citations: 5

Abstract

The authors have derived a new β-cell line (βIns2−/−lacZ) from Ins2−/− mice that carry the lacZ reporter gene under control of the Ins2 promoter. βIns2−/−lacZ cells stained positively using anti-insulin antibody, expressed β-cell–specific genes encoding the transcription factor PDX-1, glucokinase, and Glut-2, retained glucose-responsiveness for insulin secretion, and expressed the lacZ gene. Analysis of Ins1 expression by reverse transcriptase–polymerase chain reaction (RT-PCR) showed that Ins1 transcripts were significantly raised to compensate for the lack of Ins2 transcripts in βIns2−/−lacZ cells, as compared to those found in βTC1 cells expressing both Ins1/Ins2. Thus, transcriptional up-regulation of the remaining functional insulin gene in Ins2−/− mice could potentially contribute to the β-cell adaptation exhibited by these mutants, in addition to the increase in β-cell mass that we previously reported.We have also shown that lacZ expression, as analyzed by determining β-galactosidase activity, was up-regulated by incubating βIns2−/−lacZ cells with GLP-1 and/or IBMX, 2 known stimulators of insulin gene expression. These cells thus represent a new tool for testing of molecules capable of stimulating Ins2 promoter activity

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