The Transcription Factor Rfx3 Regulates β-Cell Differentiation, Function, and Glucokinase Expression

被引:55
作者
Ait-Lounis, Aouatef [1 ]
Bonal, Claire [2 ]
Seguin-Estevez, Queralt [1 ]
Schmid, Christoph D. [3 ]
Bucher, Philipp [3 ]
Herrera, Pedro L. [2 ]
Durand, Benedicte [4 ,5 ]
Meda, Paolo [6 ]
Reith, Walter [1 ]
机构
[1] Univ Geneva, CMU, Fac Med, Dept Pathol & Immunol, Geneva, Switzerland
[2] Univ Geneva, Dept Genet Med & Dev, Fac Med, Geneva, Switzerland
[3] Swiss Inst Bioinformat, Ecole Polytech Fed Lausanne, Inst Suisse Rech Expt Canc, Lausanne, Switzerland
[4] Univ Lyon, Lyon, France
[5] CNRS, Ctr Genet Mol & Cellulaire, Unite Mixte Rech 5534, Villeurbanne, France
[6] Univ Geneva, Dept Cell Physiol & Metab, Fac Med, Geneva, Switzerland
基金
瑞士国家科学基金会;
关键词
STIMULATED INSULIN-SECRETION; DNA-BINDING PROTEINS; EMBRYONIC STEM-CELLS; LEFT-RIGHT ASYMMETRY; PANCREAS DEVELOPMENT; ENDOCRINE PANCREAS; MOTOR PROTEIN; MICE LACKING; GENE; PROMOTER;
D O I
10.2337/db09-0986
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
OBJECTIVE-Pancreatic islets of perinatal mice lacking the transcription factor Rfx3 exhibit a marked reduction in insulin-producing beta-cells. The objective of this work was to unravel the cellular and molecular mechanisms underlying this deficiency. RESEARCH DESIGN AND METHODS-Immunofluorescence studies and quantitative RT-PCR experiments were used to study the emergence of insulin-positive cells, the expression of transcription factors implicated in the differentiation of beta-cells from endocrine progenitors, and the expression of mature beta-cell markers during development in Rfx3(-/-) and pancreas-specific Rfx3-knockout mice. RNA interference experiments were performed to document the consequences of downregulating Rfx3 expression in Min6 beta-cells. Quantitative chromatin immunoprecipitation (ChIP), ChIP sequencing, and bandshift experiments were used to identify Rfx3 target genes. RESULTS-Reduced development of insulin-positive cells in Rfx3(-/-) mice was not due to deficiencies in endocrine progenitors or beta-lineage specification, but reflected the accumulation of insulin-positive beta-cell precursors and defective beta-cells exhibiting reduced insulin, Glut-2, and Gck expression. Similar incompletely differentiated beta-cells developed in pancreas-specific Rfx3-deficient embryos. Defective beta-cells lacking Glut-2 and Gck expression dominate in Rfx3-deficent adults, leading to glucose intolerance. Attenuated Glut-2 and glucokinase expression, and impaired glucose-stimulated insulin secretion, were also induced by RNA interference-mediated inhibition of Rfx3 expression in Min6 cells. Finally, Rfx3 was found to bind in Min6 cells and human islets to two well-known regulatory sequences, Pal-1 and Pal-2, in the neuroendocrine promoter of the glucokinase gene. CONCLUSIONS-Our results show that Rfx3 is required for the differentiation and function of mature beta-cells and regulates the beta-cell promoter of the glucokinase gene. Diabetes 59:16741685, 2010
引用
收藏
页码:1674 / 1685
页数:12
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