BMP- and TGFβ-signaling regulate the formation of Müller glia-derived progenitor cells in the avian retina

Glia. 2017 Oct;65(10):1640-1655. doi: 10.1002/glia.23185. Epub 2017 Jul 13.

Abstract

Müller glia-derived progenitor cells (MGPCs) have the capability to regenerate neurons in the retinas of different vertebrate orders. The formation of MGPCs is regulated by a network of cell-signaling pathways. The purpose of this study was to investigate how BMP/Smad1/5/8- and TGFβ/Smad2/3-signaling are coordinated to influence the formation of MGPCs in the chick model system. We find that pSmad1/5/8 is selectively up-regulated in the nuclei of Müller glia following treatment with BMP4, FGF2, or NMDA-induced damage, and this up-regulation is blocked by a dorsomorphin analogue DMH1. By comparison, Smad2/3 is found in the nuclei of Müller glia in untreated retinas, and becomes localized to the cytoplasm following NMDA- or FGF2-treatment. These findings suggest a decrease in TGFβ- and increase in BMP-signaling when MGPCs are known to form. In both NMDA-damaged and FGF2-treated retinas, inhibition of BMP-signaling suppressed the proliferation of MGPCs, whereas inhibition of TGFβ-signaling stimulated the proliferation of MGPCs. Consistent with these findings, TGFβ2 suppressed the formation of MGPCs in NMDA-damaged retinas. Our findings indicate that BMP/TGFβ/Smad-signaling is recruited into the network of signaling pathways that controls the formation of proliferating MGPCs. We conclude that signaling through BMP4/Smad1/5/8 promotes the formation of MGPCs, whereas signaling through TGFβ/Smad2/3 suppresses the formation of MGPCs.

Keywords: BMP-signaling; Muller glia; TGFβ-signaling; regeneration; retina; retina regeneration; retinal glia.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Animals, Newborn
  • Bone Morphogenetic Protein 4 / pharmacology*
  • Bromodeoxyuridine / metabolism
  • Cell Proliferation / drug effects
  • Cell Proliferation / genetics
  • Chickens
  • Enzyme Inhibitors / pharmacology
  • Ependymoglial Cells / drug effects
  • Ependymoglial Cells / metabolism*
  • Fibroblast Growth Factor 2 / pharmacology
  • In Situ Nick-End Labeling
  • N-Methylaspartate / toxicity
  • RNA, Messenger / metabolism
  • Receptors, Transforming Growth Factor beta / antagonists & inhibitors
  • Receptors, Transforming Growth Factor beta / metabolism*
  • Retina / cytology*
  • Retina / drug effects
  • Signal Transduction / drug effects
  • Signal Transduction / physiology*
  • Smad Proteins / genetics
  • Smad Proteins / metabolism
  • Stem Cells / drug effects
  • Stem Cells / metabolism*
  • Urea / analogs & derivatives
  • Urea / metabolism

Substances

  • 1-(3-dimethylaminopropyl)-3-ethylurea
  • BMP4 protein, human
  • Bone Morphogenetic Protein 4
  • Enzyme Inhibitors
  • RNA, Messenger
  • Receptors, Transforming Growth Factor beta
  • Smad Proteins
  • Fibroblast Growth Factor 2
  • N-Methylaspartate
  • Urea
  • Bromodeoxyuridine