NUPR1 preserves insulin secretion of pancreatic β-cells during inflammatory stress by multiple low-dose streptozotocin and high-fat diet

Am J Physiol Endocrinol Metab. 2020 Aug 1;319(2):E338-E344. doi: 10.1152/ajpendo.00088.2020. Epub 2020 Jun 23.

Abstract

Obesity is associated with dyslipidemia and subclinical inflammation that promotes metabolic disturbances including insulin resistance and pancreatic β-cell dysfunction. The nuclear protein, transcriptional regulator 1 (NUPR1) responds to cellular stresses and features tissue protective properties. To characterize the role of NUPR1 in endocrine pancreatic islets during inflammatory stress, we generated transgenic mice with β-cell-specific Nupr1 overexpression (βNUPR1). Under normal conditions, βNUPR1 mice did not differ from wild type (WT) littermates and display normal glucose homeostasis and β-cell mass. For induction of inflammatory conditions, mice were treated with multiple low-dose streptozotocin (mld-STZ) and/or fed a high-fat diet (HFD). All treatments significantly worsened glycaemia in WT mice, while βNUPR1 mice substantially preserved insulin secretion and glucose tolerance. HFD increased β-cell mass in all animals, with βNUPR1 mice tending to show higher values. The improved outcome of βNUPR1 mice was accompanied by decreased NF-κB activation and lymphocyte infiltration in response to mld-STZ. In vitro, isolated βNUPR1 islets preserved insulin secretion and content with insignificantly low apoptosis during culture stress and IL-1β exposure. These findings suggest that NUPR1 plays a vital role in the protection of β-cells from apoptosis, related degradation of insulin storages and subsequent secretion during inflammatory and obesity-related tissue stress.

Keywords: IL-1β; NF-κB; NUPR1; high-fat diet; insulin secretion.

MeSH terms

  • Animals
  • Apoptosis / physiology
  • Blood Glucose / analysis
  • Cells, Cultured
  • DNA-Binding Proteins / genetics
  • DNA-Binding Proteins / physiology*
  • Diet, High-Fat / adverse effects*
  • Female
  • Gene Expression
  • Homeostasis
  • Inflammation / etiology
  • Inflammation / physiopathology*
  • Insulin Secretion / physiology*
  • Insulin-Secreting Cells / physiology*
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mice, Transgenic
  • Neoplasm Proteins / genetics
  • Neoplasm Proteins / physiology*
  • Sex Factors
  • Streptozocin / administration & dosage*

Substances

  • Blood Glucose
  • DNA-Binding Proteins
  • Neoplasm Proteins
  • Nupr1 protein, mouse
  • Streptozocin