A cell fitness selection model for neuronal survival during development.
Animals
Cell Death
/ drug effects
Cell Survival
/ drug effects
Chick Embryo
Core Binding Factor Alpha 3 Subunit
/ metabolism
Mice, Inbred C57BL
Models, Biological
Proprioception
/ drug effects
Receptor, trkC
/ metabolism
Sensory Receptor Cells
/ cytology
Signal Transduction
/ drug effects
Tretinoin
/ pharmacology
Journal
Nature communications
ISSN: 2041-1723
Titre abrégé: Nat Commun
Pays: England
ID NLM: 101528555
Informations de publication
Date de publication:
12 09 2019
12 09 2019
Historique:
received:
12
10
2018
accepted:
16
08
2019
entrez:
14
9
2019
pubmed:
14
9
2019
medline:
24
12
2019
Statut:
epublish
Résumé
Developmental cell death plays an important role in the construction of functional neural circuits. In vertebrates, the canonical view proposes a selection of the surviving neurons through stochastic competition for target-derived neurotrophic signals, implying an equal potential for neurons to compete. Here we show an alternative cell fitness selection of neurons that is defined by a specific neuronal heterogeneity code. Proprioceptive sensory neurons that will undergo cell death and those that will survive exhibit different molecular signatures that are regulated by retinoic acid and transcription factors, and are independent of the target and neurotrophins. These molecular features are genetically encoded, representing two distinct subgroups of neurons with contrasted functional maturation states and survival outcome. Thus, in this model, a heterogeneous code of intrinsic cell fitness in neighboring neurons provides differential competitive advantage resulting in the selection of cells with higher capacity to survive and functionally integrate into neural networks.
Identifiants
pubmed: 31515492
doi: 10.1038/s41467-019-12119-3
pii: 10.1038/s41467-019-12119-3
pmc: PMC6742664
doi:
Substances chimiques
Core Binding Factor Alpha 3 Subunit
0
Tretinoin
5688UTC01R
Receptor, trkC
EC 2.7.10.1
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
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