Increased basal insulin secretion in Pdzd2-deficient mice.

S W Tsang, D Shao, K S E Cheah, K Okuse, P S Leung, K-M Yao
Author Information
  1. S W Tsang: Department of Biochemistry, LKS Faculty of Medicine, The University of Hong Kong, Pokfulam, Hong Kong SAR, China.

Abstract

Expression of the multi-PDZ protein Pdzd2 (PDZ domain-containing protein 2) is enriched in pancreatic islet beta cells, but not in exocrine or alpha cells, suggesting a role for Pdzd2 in the regulation of pancreatic beta-cell function. To explore the in vivo function of Pdzd2, Pdzd2-deficient mice were generated. Homozygous Pdzd2 mutant mice were viable and their gross morphology appeared normal. Interestingly, Pdzd2-deficient mice showed enhanced glucose tolerance in intraperitoneal glucose tolerance tests and their plasma insulin levels indicated increased basal insulin secretion after fasting. Moreover, insulin release from mutant pancreatic islets was found to be twofold higher than from normal islets. To verify the functional defect in vitro, Pdzd2 was depleted in INS-1E cells using two siRNA duplexes. Pdzd2-depleted INS-1E cells also displayed increased insulin secretion at low concentrations of glucose. Our results provide the first evidence that Pdzd2 is required for normal regulation of basal insulin secretion.

MeSH Term

Animals
Blood Glucose
Body Weight
Cell Adhesion Molecules
Cells, Cultured
Gene Silencing
Glucose Tolerance Test
Insulin
Insulin Secretion
Insulin-Secreting Cells
Mice
Mice, Knockout
Nerve Tissue Proteins
Phenotype

Chemicals

Blood Glucose
Cell Adhesion Molecules
Insulin
Nerve Tissue Proteins
Pdzd2 protein, mouse

Word Cloud

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