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Hedgehog-GLI signaling regulates the behavior of cells with stem cell properties in the developing neocortex
Veronica Palma1, Ariel Ruiz i Altaba
1The Skirball Institute and Department of Cell Biology, NYU School of Medicine, 540 First Avenue, New York, NY 10016, USA.
Abstract:
Stem cells are crucial for normal development and homeostasis, and their misbehavior may be related to the origin of cancer. Progress in these areas has been difficult because the mechanisms regulating stem cell lineages are not well understood. Here, we have investigated the role of the SHH-GLI pathway in the developing mouse neocortex. The results show that SHH signaling endogenously regulates the number of embryonic and postnatal mouse neocortical cells with stem cell properties, and controls precursor proliferation in a concentration-dependent manner in cooperation with EGF signaling. These findings identify a crucial mechanism for the regulation of the number of cells with stem cell properties that is unexpectedly conserved in different stem cell niches.
Insights
Sonic hedgehog (SHH) signaling regulates the number of stem cells in the developing mouse brain. This pathway controls cell proliferation, offering insights into stem cell regulation and cancer origins.
Area of Science:
- Developmental biology
- Stem cell research
- Neuroscience
Background:
- Stem cells are vital for development and tissue maintenance.
- Dysregulation of stem cells is implicated in cancer development.
- Mechanisms controlling stem cell lineages remain incompletely understood.
Purpose of the Study:
- To investigate the role of the Sonic hedgehog-Glioma (SHH-GLI) pathway in the developing mouse neocortex.
- To elucidate how SHH signaling influences neural stem cell populations and proliferation.
Main Methods:
- Studied the SHH-GLI pathway in embryonic and postnatal mouse neocortical development.
- Analyzed the concentration-dependent effects of SHH signaling on stem and progenitor cells.
- Examined the interaction between SHH and Epidermal Growth Factor (EGF) signaling.
Main Results:
- Endogenous SHH signaling was found to regulate the number of mouse neocortical stem cells.
- SHH signaling controls precursor cell proliferation in a dose-dependent manner.
- SHH signaling cooperates with EGF signaling in regulating cell numbers.
Conclusions:
- Identified a critical mechanism for regulating the number of stem cells in the neocortex.
- The discovered regulatory mechanism is conserved across different stem cell niches.
- Findings provide a basis for understanding stem cell behavior in development and disease.
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