Pim3 negatively regulates glucose-stimulated insulin secretion

Gregory Vlacich, Martijn C. Nawijn, Gene C. Webb, Donald F. Steiner

Research output: Contribution to journalArticlepeer-review

15 Scopus citations


Pancreatic β-cell response to glucose stimulation is governed by tightly regulated signaling pathways which have not been fully characterized. A screen for novel signaling intermediates identified Pim3 as a glucose-responsive gene in the β cell, and here, we characterize its role in the regulation of β cell function. Pim3 expression in the β cell was first observed through microarray analysis on glucose-stimulated murine insulinoma (MIN6) cells where expression was strongly and transiently induced. In the pancreas, Pim3 expression exhibited similar dynamics and was restricted to the β cell. Perturbation of Pim3 function resulted in enhanced glucose-stimulated insulin secretion, both in MIN6 cells and in isolated islets from Pim3-/- mice, where the augmentation was specifically seen in the second phase of secretion. Consequently, Pim3-/- mice displayed an increased glucose tolerance in vivo. Interestingly, Pim3-/- mice also exhibited increased insulin sensitivity. Glucose stimulation of isolated Pim3 -/- islets resulted in increased phosphorylation of ERK1/2, a kinase involved in regulating β cell response to glucose. Pim3 was also found to physically interact with SOCS6 and SOCS6 levels were strongly reduced in Pim3-/- islets. Overexpression of SOCS6 inhibited glucose-induced ERK1/2 activation, strongly suggesting that Pim3 regulates ERK1/2 activity through SOCS6. These data reveal that Pim3 is a novel glucose-responsive gene in the β cell that negatively regulates insulin secretion by inhibiting the activation of ERK1/2, and through its effect on insulin sensitivity, has potentially a more global function in glucose homeostasis.

Original languageEnglish
Pages (from-to)308-317
Number of pages10
Issue number5
StatePublished - 2010


  • Beta cell
  • ERK
  • Insulin secretion
  • Pim3
  • SOCS6
  • Signal transduction


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