Frontiers in Cell and Developmental Biology (Aug 2020)

Reg-1α Promotes Differentiation of Cortical Progenitors via Its N-Terminal Active Domain

  • Marjorie Varilh,
  • Marjorie Varilh,
  • Isabelle Acquatella-Tran Van Ba,
  • Isabelle Acquatella-Tran Van Ba,
  • Michelle Silhol,
  • Michelle Silhol,
  • Francisco Nieto-Lopez,
  • Mireille Moussaed,
  • Mireille Moussaed,
  • Marie-Christine Lebart,
  • Marie-Christine Lebart,
  • Paola Bovolenta,
  • Jean-Michel Verdier,
  • Jean-Michel Verdier,
  • Mireille Rossel,
  • Mireille Rossel,
  • Anne Marcilhac,
  • Anne Marcilhac,
  • Françoise Trousse,
  • Françoise Trousse

DOI
https://doi.org/10.3389/fcell.2020.00681
Journal volume & issue
Vol. 8

Abstract

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Reg-1α belongs to the Reg family of small, secreted proteins expressed in both pancreas and nervous system. Reg-1α is composed of two domains, an insoluble C-type lectin domain and a short soluble N-terminal peptide, which is released from the molecule upon proteolytic N-terminal processing, although the biological significance of this proteolysis remains unclear. We have previously shown that binding of Reg-1α to its receptor Extl3 stimulates axonal outgrowth. Reg-1α and Extl3 genes are expressed in the developing cortex but their expression decreases in adulthood, pointing to a possible function of this signaling system at the early developmental stages. Here, we demonstrate that recombinant Reg-1α increases migration and differentiation of cultured embryonic rat telencephalic progenitors via the activation of GSK-3β activity. In vivo overexpression of Reg-1α by in utero electroporation, has a similar effect, favoring premature differentiation of cortical progenitors. Notably, the N-terminal soluble domain, but not the C-type lectin domain, is largely responsible for Reg-1α effects on cortical neuronal differentiation. We thus conclude that Reg-1α via its proteolytically generated N-terminal domain is required for basic development processes.

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