ROS Regulate Caspase-Dependent Cell Delamination without Apoptosis in the Drosophila Pupal Notum

Summary: Thorax fusion occurs in the midline of the Drosophila pupal notum and involves epithelial cell delamination requiring apoptotic signaling. By genetic screening, we found that NADPH oxidases (Nox and Duox) associated with superoxide anion (O˙-2) are responsible for caspase-3 activation and d...

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Main Authors: Yuya Fujisawa, Natsuki Shinoda, Takahiro Chihara, Masayuki Miura
Format: Article
Language:English
Published: Elsevier 2020-08-01
Series:iScience
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S2589004220306039
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spelling doaj-9f26a240415541d398be40fef82102d72020-11-25T03:42:44ZengElsevieriScience2589-00422020-08-01238101413ROS Regulate Caspase-Dependent Cell Delamination without Apoptosis in the Drosophila Pupal NotumYuya Fujisawa0Natsuki Shinoda1Takahiro Chihara2Masayuki Miura3Department of Genetics, Graduate School of Pharmaceutical Sciences, The University of Tokyo, Tokyo 113-0033, JapanDepartment of Genetics, Graduate School of Pharmaceutical Sciences, The University of Tokyo, Tokyo 113-0033, JapanDepartment of Biological Science, Graduate School of Science, Hiroshima University, Higashi-Hiroshima, Hiroshima 739-8526, Japan; Program of Biomedical Science and Basic Biology, Graduate School of Integrated Sciences for Life, Hiroshima University, Higashi-Hiroshima, Hiroshima 739-8526, JapanDepartment of Genetics, Graduate School of Pharmaceutical Sciences, The University of Tokyo, Tokyo 113-0033, Japan; Corresponding authorSummary: Thorax fusion occurs in the midline of the Drosophila pupal notum and involves epithelial cell delamination requiring apoptotic signaling. By genetic screening, we found that NADPH oxidases (Nox and Duox) associated with superoxide anion (O˙-2) are responsible for caspase-3 activation and delamination. We observed that Nox is upregulated in cells that undergo delamination and that delamination depends on caspase activation. However, the cell morphology and the almost complete lack of propidium iodide incorporation suggested little membrane disruption and signified apoptotic modulation. These results demonstrate that most delaminating cells undergo caspase activation, but this activation is not sufficient for apoptosis. We showed that the expression of Catalase, encoding an H2O2 scavenger in the cytosol, increases delamination and induces apoptotic nuclear fragmentation in caspase-3-activated cells. These findings suggest that the roles of O˙-2 and intracellular H2O2 for delamination differs before and after caspase-3 activation, which involves live cell delamination.http://www.sciencedirect.com/science/article/pii/S2589004220306039Developmental GeneticsMolecular Genetics
collection DOAJ
language English
format Article
sources DOAJ
author Yuya Fujisawa
Natsuki Shinoda
Takahiro Chihara
Masayuki Miura
spellingShingle Yuya Fujisawa
Natsuki Shinoda
Takahiro Chihara
Masayuki Miura
ROS Regulate Caspase-Dependent Cell Delamination without Apoptosis in the Drosophila Pupal Notum
iScience
Developmental Genetics
Molecular Genetics
author_facet Yuya Fujisawa
Natsuki Shinoda
Takahiro Chihara
Masayuki Miura
author_sort Yuya Fujisawa
title ROS Regulate Caspase-Dependent Cell Delamination without Apoptosis in the Drosophila Pupal Notum
title_short ROS Regulate Caspase-Dependent Cell Delamination without Apoptosis in the Drosophila Pupal Notum
title_full ROS Regulate Caspase-Dependent Cell Delamination without Apoptosis in the Drosophila Pupal Notum
title_fullStr ROS Regulate Caspase-Dependent Cell Delamination without Apoptosis in the Drosophila Pupal Notum
title_full_unstemmed ROS Regulate Caspase-Dependent Cell Delamination without Apoptosis in the Drosophila Pupal Notum
title_sort ros regulate caspase-dependent cell delamination without apoptosis in the drosophila pupal notum
publisher Elsevier
series iScience
issn 2589-0042
publishDate 2020-08-01
description Summary: Thorax fusion occurs in the midline of the Drosophila pupal notum and involves epithelial cell delamination requiring apoptotic signaling. By genetic screening, we found that NADPH oxidases (Nox and Duox) associated with superoxide anion (O˙-2) are responsible for caspase-3 activation and delamination. We observed that Nox is upregulated in cells that undergo delamination and that delamination depends on caspase activation. However, the cell morphology and the almost complete lack of propidium iodide incorporation suggested little membrane disruption and signified apoptotic modulation. These results demonstrate that most delaminating cells undergo caspase activation, but this activation is not sufficient for apoptosis. We showed that the expression of Catalase, encoding an H2O2 scavenger in the cytosol, increases delamination and induces apoptotic nuclear fragmentation in caspase-3-activated cells. These findings suggest that the roles of O˙-2 and intracellular H2O2 for delamination differs before and after caspase-3 activation, which involves live cell delamination.
topic Developmental Genetics
Molecular Genetics
url http://www.sciencedirect.com/science/article/pii/S2589004220306039
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AT takahirochihara rosregulatecaspasedependentcelldelaminationwithoutapoptosisinthedrosophilapupalnotum
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