c-Cbl Regulates Murine Subventricular Zone-Derived Neural Progenitor Cells in Dependence of the Epidermal Growth Factor Receptor

Research output: Contribution to journalResearch articleContributedpeer-review

Contributors

Abstract

The localization, expression, and physiological role of regulatory proteins in the neurogenic niches of the brain is fundamental to our understanding of adult neurogenesis. This study explores the expression and role of the E3-ubiquitin ligase, c-Cbl, in neurogenesis within the subventricular zone (SVZ) of mice. In vitro neurosphere assays and in vivo analyses were performed in specific c-Cbl knock-out lines to unravel c-Cbl’s role in receptor tyrosine kinase signaling, including the epidermal growth factor receptor (EGFR) pathway. Our findings suggest that c-Cbl is significantly expressed within EGFR-expressing cells, playing a pivotal role in neural stem cell proliferation and differentiation. However, c-Cbl’s function extends beyond EGFR signaling, as its loss upon knock-out stimulated progenitor cell proliferation in neurosphere cultures. Yet, this effect was not detected in hippocampal progenitor cells, reflecting the lack of the EGFR in the hippocampus. In vivo, c-Cbl exerted only a minor proneurogenic influence with no measurable impact on the formation of adult-born neurons. In conclusion, c-Cbl regulates neural stem cells in the subventricular zone via the EGFR pathway but, likely, its loss is compensated by other signaling modules in vivo.

Details

Original languageEnglish
Article number2400
JournalCells
Volume12
Issue number19
Publication statusPublished - 3 Oct 2023
Peer-reviewedYes

External IDs

Scopus 85173880407
PubMed 37830613

Keywords

Keywords

  • Animals, Mice, Cell Differentiation, ErbB Receptors/metabolism, Lateral Ventricles/metabolism, Neural Stem Cells/metabolism, Neurons/metabolism, Proto-Oncogene Proteins c-cbl/genetics