Mechanisms of β-cell functional adaptation to changes in workload

Diabetes Obes Metab. 2016 Sep;18 Suppl 1(Suppl 1):78-86. doi: 10.1111/dom.12729.

Abstract

Insulin secretion must be tightly coupled to nutritional state to maintain blood glucose homeostasis. To this end, pancreatic β-cells sense and respond to changes in metabolic conditions, thereby anticipating insulin demands for a given physiological context. This is achieved in part through adjustments of nutrient metabolism, which is controlled at several levels including allosteric regulation, post-translational modifications, and altered expression of metabolic enzymes. In this review, we discuss mechanisms of β-cell metabolic and functional adaptation in the context of two physiological states that alter glucose-stimulated insulin secretion: fasting and insulin resistance. We review current knowledge of metabolic changes that occur in the β-cell during adaptation and specifically discuss transcriptional mechanisms that underlie β-cell adaptation. A more comprehensive understanding of how β-cells adapt to changes in nutrient state could identify mechanisms to be co-opted for therapeutically modulating insulin secretion in metabolic disease.

Keywords: adaptation; fasting; insulin resistance; insulin secretion; metabolism; transcription; β-cell.

Publication types

  • Review

MeSH terms

  • Adaptation, Physiological*
  • Allosteric Regulation
  • Animals
  • Blood Glucose / metabolism*
  • Fasting / metabolism*
  • Gene Expression Regulation*
  • Homeostasis
  • Humans
  • Insulin / metabolism*
  • Insulin Resistance / genetics*
  • Insulin Secretion
  • Insulin-Secreting Cells / metabolism*
  • Protein Processing, Post-Translational*

Substances

  • Blood Glucose
  • Insulin