Searching across hundreds of databases

Our searching services are busy right now. Your search will reload in five seconds.

X
Forgot Password

If you have forgotten your password you can enter your email here and get a temporary password sent to your email.

X
Forgot Password

If you have forgotten your password you can enter your email here and get a temporary password sent to your email.

Clobetasol Modulates Adult Neural Stem Cell Growth via Canonical Hedgehog Pathway Activation.

International journal of molecular sciences | 2019

Sonic hedgehog (Shh) signaling is a key pathway within the central nervous system (CNS), during both development and adulthood, and its activation via the 7-transmembrane protein Smoothened (Smo) may promote neuroprotection and restoration during neurodegenerative disorders. Shh signaling may also be activated by selected glucocorticoids such as clobetasol, fluocinonide and fluticasone, which therefore act as Smo agonists and hold potential utility for regenerative medicine. However, despite its potential role in neurodegenerative diseases, the impact of Smo-modulation induced by these glucocorticoids on adult neural stem cells (NSCs) and the underlying signaling mechanisms are not yet fully elucidated. The aim of the present study was to evaluate the effects of Smo agonists (i.e., purmorphamine) and antagonists (i.e., cyclopamine) as well as of glucocorticoids (i.e., clobetasol, fluocinonide and fluticasone) on NSCs in terms of proliferation and clonal expansion. Purmorphamine treatment significantly increased NSC proliferation and clonal expansion via GLI-Kruppel family member 1 (Gli1) nuclear translocation and such effects were prevented by cyclopamine co-treatment. Clobetasol treatment exhibited an equivalent pharmacological effect. Moreover, cellular thermal shift assay suggested that clobetasol induces the canonical Smo-dependent activation of Shh signaling, as confirmed by Gli1 nuclear translocation and also by cyclopamine co-treatment, which abolished these effects. Finally, fluocinonide and fluticasone as well as control glucocorticoids (i.e., prednisone, corticosterone and dexamethasone) showed no significant effects on NSCs proliferation and clonal expansion. In conclusion, our data suggest that Shh may represent a druggable target system to drive neuroprotection and promote restorative therapies.

Pubmed ID: 31018557 RIS Download

Publication data is provided by the National Library of Medicine ® and PubMed ®. Data is retrieved from PubMed ® on a weekly schedule. For terms and conditions see the National Library of Medicine Terms and Conditions.

This is a list of tools and resources that we have found mentioned in this publication.


129/Sv (tool)

RRID:MGI:2161069

laboratory mouse with name 129/Sv from MGI.

View all literature mentions

Anti-SOX2 antibody (antibody)

RRID:AB_2341193

This polyclonal targets sox2

View all literature mentions

Smoothened antibody (antibody)

RRID:AB_1270802

This polyclonal targets Smoothened antibody

View all literature mentions

Anti-Nestin antibody (antibody)

RRID:AB_2753197

This polyclonal targets Nestin

View all literature mentions

Anti-SOX2 antibody (antibody)

RRID:AB_2341193

This polyclonal targets sox2

View all literature mentions

Smoothened antibody (antibody)

RRID:AB_1270802

This polyclonal targets Smoothened antibody

View all literature mentions

Smoothened antibody (antibody)

RRID:AB_1270802

This polyclonal targets Smoothened antibody

View all literature mentions

Anti-Nestin antibody (antibody)

RRID:AB_2753197

This polyclonal targets Nestin

View all literature mentions

Anti-Nestin antibody (antibody)

RRID:AB_2753197

This polyclonal targets Nestin

View all literature mentions

Anti-SOX2 antibody (antibody)

RRID:AB_2341193

This polyclonal targets sox2

View all literature mentions