| Glucose regulates LXRα subcellular localization and function in rat pancreatic β-cells |
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| 引用本文： | Helleboid-Chapman A,Helleboid S,Jakel H,Timmerman C,Sergheraert C,Pattou F,Fruchart-Najib J,Fruchart JC. Glucose regulates LXRα subcellular localization and function in rat pancreatic β-cells[J]. Cell research, 2006, 16(7): 661-670 |
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| 作者姓名： | Helleboid-Chapman A Helleboid S Jakel H Timmerman C Sergheraert C Pattou F Fruchart-Najib J Fruchart JC |
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| 作者单位： | Atherosclerosis Department UR 545 INSERM,the Faculty of Pharmacy,Lille 2 University,1 rue du Professeur Calmette BP245,Lille cedex 59019,France,Atherosclerosis Department,UR 545 INSERM,the Faculty of Pharmacy,Lille 2 University,1 rue du Professeur Calmette BP245,Lille cedex 59019,France,Atherosclerosis Department,UR 545 INSERM,the Faculty of Pharmacy,Lille 2 University,1 rue du Professeur Calmette BP245,Lille cedex 59019,France,Synthesis,Structure and Biomolecule Function,UMR 8525 CNRS,Pasteur Institute of Lille,Lille 2 University,Lille,France,Cell Therapy for Diabetes,ERIT-M 0106,Faculty,of Medecine University of Lille 2/INSERM,Lille 59045,France,Atherosclerosis Department,UR 545 INSERM,the Faculty of Pharmacy,Lille 2 University,1 rue du Professeur Calmette BP245,Lille cedex 59019,France,Atherosclerosis Department,UR 545 INSERM,the Faculty of Pharmacy,Lille 2 University,1 rue du Professeur Calmette BP245,Lille cedex 59019,France |
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| 基金项目： | Acknowledgment This work was supported by research grants from Leducq foundation （02CVD02）. |
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| 摘 要： | Liver X receptors （LXRs） are members of the nuclear receptor superfamily, which have been implicated in lipid homeostasis and more recently in glucose metabolism. Here, we show that glucose does not change LXRα protein level, but affects its localization in pancreatic β-cells. LXRα is found in the nucleus at 8 mM glucose and in the cytoplasm at 4.2 mM. Addition of glucose translocates LXRα from the cytoplasm into the nucleus. Moreover, after the activation of LXR by its synthetic non-steroidal agonist （T0901317）, insulin secretion and glucose uptake are increased at 8 mM and decreased at 4.2 mM glucose in a dose-dependent manner. Furthermore, at low glucose condition, okadaic acid reversed LXRα effect on insulin secretion, suggesting the involvement of glucose signaling through a phosphorylation-dependent mechanism.
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| 关 键 词： | LXRα 葡萄糖 亚细胞 胰腺β-细胞 |
| 收稿时间： | 2005-10-06 |
| 修稿时间： | 2005-10-062006-04-25 |
Glucose regulates LXRalpha subcellular localization and function in rat pancreatic beta-cells |
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| Helleboid-Chapman Audrey,Helleboid Stéphane,Jakel Heidelinde,Timmerman Catherine,Sergheraert Christian,Pattou François,Fruchart-Najib Jamila,Fruchart Jean-Charles. Glucose regulates LXRalpha subcellular localization and function in rat pancreatic beta-cells[J]. Cell research, 2006, 16(7): 661-670 |
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| Authors: | Helleboid-Chapman Audrey Helleboid Stéphane Jakel Heidelinde Timmerman Catherine Sergheraert Christian Pattou François Fruchart-Najib Jamila Fruchart Jean-Charles |
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| Affiliation: | Atherosclerosis Department, UR 545 INSERM, the Faculty of Pharmacy, Lille 2 University, 1 rue du Professeur Calmette BP245, Lille cedex 59019, France. audrey.chapman@pasteur-lille.fr |
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| Abstract: | Liver X receptors (LXRs) are members of the nuclear receptor superfamily, which have been implicated in lipid homeostasis and more recently in glucose metabolism. Here, we show that glucose does not change LXRalpha protein level, but affects its localization in pancreatic beta-cells. LXRalpha is found in the nucleus at 8 mM glucose and in the cytoplasm at 4.2 mM. Addition of glucose translocates LXRalpha from the cytoplasm into the nucleus. Moreover, after the activation of LXR by its synthetic non-steroidal agonist (T0901317), insulin secretion and glucose uptake are increased at 8 mM and decreased at 4.2 mM glucose in a dose-dependent manner. Furthermore, at low glucose condition, okadaic acid reversed LXRalpha effect on insulin secretion, suggesting the involvement of glucose signaling through a phosphorylation-dependent mechanism. |
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