Characterization of the expression, localization, and secretion of PANDER in alpha-cells

Mol Cell Endocrinol. 2010 Aug 30;325(1-2):36-45. doi: 10.1016/j.mce.2010.05.008.

Abstract

The novel islet-specific protein PANcreatic DERived Factor (PANDER; FAM3B) has been extensively characterized with respect to the beta-cell, and these studies suggest a potential function for PANDER in the regulation of glucose homeostasis. Little is known regarding PANDER in pancreatic -cells, which are critically involved in maintaining euglycemia. Here we present the first report elucidating the expression and regulation of PANDER within the alpha-cell. Pander mRNA and protein are detected in alpha-cells, with primary localization to a glucagon-negative granular cytosolic compartment. PANDER secretion from alpha-cells is nutritionally and hormonally regulated by l-arginine and insulin, demonstrating similarities and differences with glucagon. Signaling via the insulin receptor (IR) through the PI3K and Akt/PKB node is required for insulin-stimulated PANDER release. The separate localization of PANDER and glucagon is consistent with their differential regulation, and the effect of insulin suggests a paracrine/endocrine effect on PANDER release. This provides further insight into the potential glucose-regulatory role of PANDER.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Arginine / pharmacology
  • Cell Culture Techniques
  • Cells, Cultured
  • Cytokines / genetics*
  • Cytokines / metabolism*
  • Dose-Response Relationship, Drug
  • Gene Expression
  • Glucagon-Secreting Cells / drug effects
  • Glucagon-Secreting Cells / metabolism*
  • Glucose / pharmacology
  • In Situ Hybridization, Fluorescence
  • Insulin / metabolism
  • Insulin / pharmacology
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Paracrine Communication / drug effects
  • Paracrine Communication / physiology
  • Tissue Distribution

Substances

  • Cytokines
  • Insulin
  • PANDER protein, mouse
  • Arginine
  • Glucose