PUBLICATION

Deterministic fate assignment of Müller glia cells in the zebrafish retina suggest a clonal backbone during development

Authors
Rulands, S., Iglesias Gonzalez, A.B., Boije, H.
ID
ZDB-PUB-181109-9
Date
2018
Source
The European journal of neuroscience   48(12): 3597-3605 (Journal)
Registered Authors
Keywords
Danio rerio, GFAP, Retinal progenitor cell, bipolar cell, stochastic
MeSH Terms
  • Animals
  • Animals, Genetically Modified/genetics
  • Cell Differentiation/physiology
  • Cell Proliferation/physiology
  • Ependymoglial Cells/metabolism*
  • Neurogenesis/physiology
  • Neuroglia/metabolism*
  • Neurons/metabolism
  • Retina/metabolism*
  • Stem Cells/metabolism*
  • Zebrafish/metabolism
  • Zebrafish Proteins/metabolism
PubMed
30408243 Full text @ Eur. J. Neurosci.
Abstract
The optic cup houses multipotent retinal progenitor cells that proliferate and differentiate to form the mature retina, containing five main types of neurons and a single glial cell type, the Müller cell. Progenitors of the zebrafish optic cup generate clones that varies regarding the number and types of neurons, a process we previously showed could be described by stochastic models. Here, we present data indicating that each retinal progenitor cell, in the 24 hours post-fertilization optic cup, is predestined to form a single Müller cell. This striking fate assignment of Müller cells reveal a dual nature of retinal lineages where stochastic mechanisms produce variable numbers of neurons while there is a strong deterministic component governing the formation of glia cells. A possible mechanism for this stereotypic fate assignment could be the maintenance of a clonal backbone during retina development, which would be similar to invertebrate and rodent cortical neurogenesis. This article is protected by copyright. All rights reserved.
Genes / Markers
Figures
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Antibodies
Orthology
Engineered Foreign Genes
Mapping