The Pax4 gene is essential for differentiation of insulin-producing β cells in the mammalian pancreas

Beatriz Sosa-Pineda, Kamal Chowdhury, Miguel Torres, Guillermo Oliver and Peter Gruss
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Beatriz Sosa-Pineda: Max Planck Institute for Biophysical Chemistry
Kamal Chowdhury: Max Planck Institute for Biophysical Chemistry
Miguel Torres: Max Planck Institute for Biophysical Chemistry
Guillermo Oliver: Max Planck Institute for Biophysical Chemistry
Peter Gruss: Max Planck Institute for Biophysical Chemistry

Nature, 1997, vol. 386, issue 6623, 399-402

Abstract: Abstract The mammalian pancreas contains two distinct cell populations: endocrine cells which secrete hormones into the bloodstream, and exocrine cells, which secrete enzymes into the digestive tract1. The four endocrine cell types found in the adult pancreas—α, β, δ and PP—synthesize glucagon, insulin, somatostatin and pancreatic polypeptide, respectively2. All of these endocrine cells arise from common multipotent precursors, which coexpress several hormones when they start to differentiate3. Expression of some homeobox genes in the early developing pancreas has been reported4–7. The Pax4 gene is expressed in the early pancreas, but is later restricted to βcells. Inactivation of Pax4 by homologous recombination results in the absence of mature insulin-and somatostatin-producing cells (β and δ, respectively) in the pancreas of Pax4 homozygous mutant mice, but glucagon-producing α cells are present in considerably higher numbers. We propose that the early expression of Pax4 in a subset of endocrine progenitors is essential for the differentiation of the β and δ cell lineages. A default pathway would explain the elevated number of α cells in the absence of Pax4.

Date: 1997
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DOI: 10.1038/386399a0

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