Pax6 Inactivation in the Adult Pancreas Reveals Ghrelin as Endocrine Cell Maturation Marker

PLoS One. 2015 Dec 11;10(12):e0144597. doi: 10.1371/journal.pone.0144597. eCollection 2015.

Abstract

The transcription factor Pax6 is an important regulator of development and cell differentiation in various organs. Thus, Pax6 was shown to promote neural development in the cerebral cortex and spinal cord, and to control pancreatic endocrine cell genesis. However, the role of Pax6 in distinct endocrine cells of the adult pancreas has not been addressed. We report the conditional inactivation of Pax6 in insulin and glucagon producing cells of the adult mouse pancreas. In the absence of Pax6, beta- and alpha-cells lose their molecular maturation characteristics. Our findings provide strong evidence that Pax6 is responsible for the maturation of beta-, and alpha-cells, but not of delta-, and PP-cells. Moreover, lineage-tracing experiments demonstrate that Pax6-deficient beta- and alpha-cells are shunted towards ghrelin marked cells, sustaining the idea that ghrelin may represent a marker for endocrine cell maturation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Bacterial Proteins / genetics
  • Bacterial Proteins / metabolism
  • Cell Differentiation
  • Cell Lineage / drug effects
  • Cell Lineage / genetics
  • Crosses, Genetic
  • Eye Proteins / genetics*
  • Eye Proteins / metabolism
  • Female
  • Gene Expression Regulation, Developmental
  • Genes, Reporter
  • Ghrelin / genetics*
  • Ghrelin / metabolism
  • Glucagon-Secreting Cells / cytology
  • Glucagon-Secreting Cells / drug effects
  • Glucagon-Secreting Cells / metabolism*
  • Homeodomain Proteins / genetics*
  • Homeodomain Proteins / metabolism
  • Insulin / genetics
  • Insulin / metabolism
  • Insulin-Secreting Cells / cytology
  • Insulin-Secreting Cells / drug effects
  • Insulin-Secreting Cells / metabolism*
  • Integrases / genetics
  • Integrases / metabolism
  • Luminescent Proteins / genetics
  • Luminescent Proteins / metabolism
  • Male
  • Mice
  • Mice, Knockout
  • PAX6 Transcription Factor
  • Paired Box Transcription Factors / genetics*
  • Paired Box Transcription Factors / metabolism
  • Pancreatic Polypeptide-Secreting Cells / cytology
  • Pancreatic Polypeptide-Secreting Cells / drug effects
  • Pancreatic Polypeptide-Secreting Cells / metabolism*
  • Repressor Proteins / genetics*
  • Repressor Proteins / metabolism
  • Signal Transduction
  • Somatostatin-Secreting Cells / cytology
  • Somatostatin-Secreting Cells / drug effects
  • Somatostatin-Secreting Cells / metabolism*
  • Tamoxifen / pharmacology

Substances

  • Bacterial Proteins
  • Eye Proteins
  • Ghrelin
  • Homeodomain Proteins
  • Insulin
  • Luminescent Proteins
  • PAX6 Transcription Factor
  • Paired Box Transcription Factors
  • Pax6 protein, mouse
  • Repressor Proteins
  • yellow fluorescent protein, Bacteria
  • Tamoxifen
  • Cre recombinase
  • Integrases

Grants and funding

This work was supported by the Max-Planck Society, the Juvenile Diabetes Research foundation (17-2011-16, 2-2010-567, 26-2008-639, 17-2013-426), the INSERM AVENIR program, the INSERM, the European Research Council (StG-2011-281265) the FMR (DRC20091217179), the ANR/BMBF (2009 GENO 105 01/01KU0906), the ‘‘Investments for the Future’’ LABEX SIGNALIFE (ANR-11-LABX-0028-01), Club Isatis, Mr. and Mrs. Dorato, the Fondation Générale de Santé, and the Foundation Schlumberger pour l’Education et la Recherche.