Caspase-dependent activation of Hedgehog-signalling sustains proliferation and differentiation of ovarian somatic stem cells

There is increasing evidence associating the role of caspases with the regulation of basic cellular functions beyond apoptosis. However, the molecular interplay between these enzymes and the signalling networks active in non-apoptotic cellular scenarios remains largely uncharacterized. Here, we show...

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Main Authors: Baena-Lopez, LA, Galasso, A, Iakovleva, D
Format: Journal article
Language:English
Published: Cold Spring Harbor Laboratory 2019
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author Baena-Lopez, LA
Galasso, A
Iakovleva, D
author_facet Baena-Lopez, LA
Galasso, A
Iakovleva, D
author_sort Baena-Lopez, LA
collection OXFORD
description There is increasing evidence associating the role of caspases with the regulation of basic cellular functions beyond apoptosis. However, the molecular interplay between these enzymes and the signalling networks active in non-apoptotic cellular scenarios remains largely uncharacterized. Here, we show that transient and non-apoptotic caspase activation facilitates Hedgehog-signalling in Drosophila and human ovarian cells with a somatic origin. Importantly, this novel caspase function controls gene expression, cell proliferation, and differentiation. We also molecularly link this uncovered caspase role with the fine regulation of the Hedgehog-receptor, Patched. Altogether, these findings strikingly suggest that caspase activation can act as a pro-survival factor that promotes the expansion and differentiation of normal healthy cells. These observations have profound implications on our understanding of caspase biology from a cellular, physiological and evolutionary perspective.
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spelling oxford-uuid:4d24bfce-20ff-4948-b044-854d30fffe3d2022-03-26T15:53:45ZCaspase-dependent activation of Hedgehog-signalling sustains proliferation and differentiation of ovarian somatic stem cellsJournal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:4d24bfce-20ff-4948-b044-854d30fffe3dEnglishSymplectic ElementsCold Spring Harbor Laboratory2019Baena-Lopez, LAGalasso, AIakovleva, DThere is increasing evidence associating the role of caspases with the regulation of basic cellular functions beyond apoptosis. However, the molecular interplay between these enzymes and the signalling networks active in non-apoptotic cellular scenarios remains largely uncharacterized. Here, we show that transient and non-apoptotic caspase activation facilitates Hedgehog-signalling in Drosophila and human ovarian cells with a somatic origin. Importantly, this novel caspase function controls gene expression, cell proliferation, and differentiation. We also molecularly link this uncovered caspase role with the fine regulation of the Hedgehog-receptor, Patched. Altogether, these findings strikingly suggest that caspase activation can act as a pro-survival factor that promotes the expansion and differentiation of normal healthy cells. These observations have profound implications on our understanding of caspase biology from a cellular, physiological and evolutionary perspective.
spellingShingle Baena-Lopez, LA
Galasso, A
Iakovleva, D
Caspase-dependent activation of Hedgehog-signalling sustains proliferation and differentiation of ovarian somatic stem cells
title Caspase-dependent activation of Hedgehog-signalling sustains proliferation and differentiation of ovarian somatic stem cells
title_full Caspase-dependent activation of Hedgehog-signalling sustains proliferation and differentiation of ovarian somatic stem cells
title_fullStr Caspase-dependent activation of Hedgehog-signalling sustains proliferation and differentiation of ovarian somatic stem cells
title_full_unstemmed Caspase-dependent activation of Hedgehog-signalling sustains proliferation and differentiation of ovarian somatic stem cells
title_short Caspase-dependent activation of Hedgehog-signalling sustains proliferation and differentiation of ovarian somatic stem cells
title_sort caspase dependent activation of hedgehog signalling sustains proliferation and differentiation of ovarian somatic stem cells
work_keys_str_mv AT baenalopezla caspasedependentactivationofhedgehogsignallingsustainsproliferationanddifferentiationofovariansomaticstemcells
AT galassoa caspasedependentactivationofhedgehogsignallingsustainsproliferationanddifferentiationofovariansomaticstemcells
AT iakovlevad caspasedependentactivationofhedgehogsignallingsustainsproliferationanddifferentiationofovariansomaticstemcells