Imperial College London
Alternate

DrIsabelleLeclerc

Faculty of Medicine, Department of Metabolism, Digestion and Reproduction

Visiting Professor
 
 
 
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Contact

 

+44 (0)20 7594 3354i.leclerc

 
 
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Location

 

323ICTEM buildingHammersmith Campus

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Summary

 

Publications

Citation

BibTex format

@article{Nguyen-Tu:2018:10.1074/jbc.RA118.003613,
author = {Nguyen-Tu, M-S and da, Silva Xavier G and Leclerc, I and Rutter, GA},
doi = {10.1074/jbc.RA118.003613},
journal = {Journal of Biological Chemistry},
pages = {14178--14189},
title = {Transcription factor-7-like 2 (TCF7L2) gene acts downstream of the Lkb1/Stk11 kinase to control mTOR signaling, β cell growth, and insulin secretion},
url = {http://dx.doi.org/10.1074/jbc.RA118.003613},
volume = {293},
year = {2018}
}
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RIS format (EndNote, RefMan)

TY  - JOUR
AB  - Variants in the transcription factor-7-like 2 (TCF7L2/TCF4) gene, involved in Wnt signalling, are associated with type 2 diabetes. Loss of Tcf7l2 selectively from the β cell in mice has previously been shown to cause glucose intolerance and to lower β cell mass. Deletion of the tumour suppressor liver kinase B1 (LKB1/STK11) leads to β cell hyperplasia and enhanced glucose-stimulated insulin secretion, providing a convenient genetic model for increased β cell growth and function. The aim of this study was to explore the possibility that Tcf7l2 may be required for the effects of Lkb1 deletion on insulin secretion in the mouse β cell. Mice bearing floxed Lkb1 and/or Tcf7l2 alleles were bred with knock-in mice bearing Cre recombinase inserted at the Ins1 locus (Ins1Cre), allowing highly β cell-selective deletion of either or both genes. Oral glucose tolerance was unchanged by the further deletion of a single Tcf7l2 allele in these cells. By contrast, mice lacking both Tcf7l2 alleles on this background showed improved oral glucose tolerance and insulin secretion in vivo and in vitro compared to mice lacking a single Tcf7l2 allele. Bi-allelic Tcf7l2 deletion also enhanced β cell proliferation, increased β cell mass and caused changes in polarity as revealed by the "rosette-like" arrangement of β cells. Tcf7l2 deletion also increased signalling by Target of Rapamycin (mTOR), augmenting phospho-ribosomal S6 levels. We identified a novel signalling mechanism through which a modifier gene, Tcf7l2, lies on a pathway through which LKB1 acts in the β cell to restrict insulin secretion.
AU  - Nguyen-Tu,M-S
AU  - da,Silva Xavier G
AU  - Leclerc,I
AU  - Rutter,GA
DO  - 10.1074/jbc.RA118.003613
EP  - 14189
PY  - 2018///
SN  - 0021-9258
SP  - 14178
TI  - Transcription factor-7-like 2 (TCF7L2) gene acts downstream of the Lkb1/Stk11 kinase to control mTOR signaling, β cell growth, and insulin secretion
T2  - Journal of Biological Chemistry
UR  - http://dx.doi.org/10.1074/jbc.RA118.003613
UR  - https://www.ncbi.nlm.nih.gov/pubmed/29967064
UR  - http://www.jbc.org/content/293/36/14178
UR  - http://hdl.handle.net/10044/1/61951
VL  - 293
ER  -
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