Role of BH3-Only Molecules Bim and Puma in β-Cell Death in Pdx1 Deficiency

Autor: Changzheng Wang, Honggang Ye, Kenneth S. Polonsky, Liqun Mao, Juan Sun, Emily H. Cheng, Decheng Ren, Graeme I. Bell
Rok vydání: 2014
Předmět:
endocrine system
Programmed cell death
endocrine system diseases
Endocrinology
Diabetes and Metabolism

Apoptosis
Biology
digestive system
Cell Line
Transcriptome
Mice
03 medical and health sciences
0302 clinical medicine
Downregulation and upregulation
RNA interference
Insulin-Secreting Cells
Proto-Oncogene Proteins
hemic and lymphatic diseases
Puma
Internal Medicine
Animals
RNA
Messenger

RNA
Small Interfering

030304 developmental biology
Homeodomain Proteins
0303 health sciences
Bcl-2-Like Protein 11
Tumor Suppressor Proteins
Lentivirus
Membrane Proteins
biology.organism_classification
Molecular biology
Up-Regulation
Islet Studies
Haplotypes
Cell culture
Gene Knockdown Techniques
030220 oncology & carcinogenesis
Trans-Activators
Cancer research
PDX1
RNA Interference
biological phenomena
cell phenomena
and immunity

Apoptosis Regulatory Proteins
Zdroj: Diabetes
ISSN: 1939-327X
0012-1797
Popis: Mutations in pancreatic duodenal homeobox-1 (PDX1) are associated with diabetes in humans. Pdx1-haploinsufficient mice develop diabetes due to an increase in β-cell death leading to reduced β-cell mass. For definition of the molecular link between Pdx1 deficiency and β-cell death, Pdx1-haploinsufficient mice in which the genes for the BH3-only molecules Bim and Puma had been ablated were studied on a high-fat diet. Compared with Pdx1+/− mice, animals haploinsufficient for both Pdx1 and Bim or Puma genes showed improved glucose tolerance, enhanced β-cell mass, and reduction in the number of TUNEL-positive cells in islets. These results suggest that Bim and Puma ablation improves β-cell survival in Pdx1+/− mice. For exploration of the mechanisms responsible for these findings, Pdx1 gene expression was knocked down in mouse MIN6 insulinoma cells resulting in apoptotic cell death that was found to be associated with increased expression of BH3-only molecules Bim and Puma. If the upregulation of Bim and Puma that occurs during Pdx1 suppression was prevented, apoptotic β-cell death was reduced in vitro. These results suggest that Bim and Puma play an important role in β-cell apoptosis in Pdx1-deficient diabetes.
Databáze: OpenAIRE