An Activating STAT3 Mutation Causes Neonatal Diabetes through Premature Induction of Pancreatic Differentiation

Cell Rep. 2017 Apr 11;19(2):281-294. doi: 10.1016/j.celrep.2017.03.055.

Abstract

Activating germline mutations in STAT3 were recently identified as a cause of neonatal diabetes mellitus associated with beta-cell autoimmunity. We have investigated the effect of an activating mutation, STAT3K392R, on pancreatic development using induced pluripotent stem cells (iPSCs) derived from a patient with neonatal diabetes and pancreatic hypoplasia. Early pancreatic endoderm differentiated similarly from STAT3K392R and healthy-control cells, but in later stages, NEUROG3 expression was upregulated prematurely in STAT3K392R cells together with insulin (INS) and glucagon (GCG). RNA sequencing (RNA-seq) showed robust NEUROG3 downstream targets upregulation. STAT3 mutation correction with CRISPR/Cas9 reversed completely the disease phenotype. STAT3K392R-activating properties were not explained fully by altered DNA-binding affinity or increased phosphorylation. Instead, reporter assays demonstrated NEUROG3 promoter activation by STAT3 in pancreatic cells. Furthermore, proteomic and immunocytochemical analyses revealed increased nuclear translocation of STAT3K392R. Collectively, our results demonstrate that the STAT3K392R mutation causes premature endocrine differentiation through direct induction of NEUROG3 expression.

Keywords: CRISPR; NEUROG3; STAT3; beta cell; endocrine cells; genome editing; iPSC; monogenic diabetes; pancreatic differentiation; stem cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Autoimmunity / genetics
  • Basic Helix-Loop-Helix Transcription Factors / biosynthesis*
  • Basic Helix-Loop-Helix Transcription Factors / genetics
  • CRISPR-Cas Systems
  • Cell Differentiation / genetics*
  • Cell Line
  • Diabetes Mellitus / etiology
  • Diabetes Mellitus / genetics*
  • Diabetes Mellitus / pathology
  • Gene Expression Regulation, Developmental
  • Glucagon / metabolism
  • Humans
  • Induced Pluripotent Stem Cells / metabolism
  • Induced Pluripotent Stem Cells / pathology
  • Insulin / genetics
  • Insulin / metabolism
  • Insulin-Secreting Cells / metabolism
  • Insulin-Secreting Cells / pathology
  • Mutation
  • Nerve Tissue Proteins / biosynthesis*
  • Nerve Tissue Proteins / genetics
  • Promoter Regions, Genetic
  • STAT3 Transcription Factor / biosynthesis
  • STAT3 Transcription Factor / genetics*

Substances

  • Basic Helix-Loop-Helix Transcription Factors
  • Insulin
  • NEUROG3 protein, human
  • Nerve Tissue Proteins
  • STAT3 Transcription Factor
  • STAT3 protein, human
  • Glucagon