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The Function of Autophagy in Lace Plant Programmed Cell Death
The lace plant (Aponogeton madagascariensis) is an aquatic monocot that utilizes programmed cell death (PCD) to form perforations throughout its mature leaves as part of normal development. The lace plant is an emerging model system representing a unique form of developmental PCD. The role of autoph...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6817616/ https://www.ncbi.nlm.nih.gov/pubmed/31695708 http://dx.doi.org/10.3389/fpls.2019.01198 |
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author | Dauphinee, Adrian N. Denbigh, Georgia L. Rollini, Alice Fraser, Meredith Lacroix, Christian R. Gunawardena, Arunika H. L. A. N. |
author_facet | Dauphinee, Adrian N. Denbigh, Georgia L. Rollini, Alice Fraser, Meredith Lacroix, Christian R. Gunawardena, Arunika H. L. A. N. |
author_sort | Dauphinee, Adrian N. |
collection | PubMed |
description | The lace plant (Aponogeton madagascariensis) is an aquatic monocot that utilizes programmed cell death (PCD) to form perforations throughout its mature leaves as part of normal development. The lace plant is an emerging model system representing a unique form of developmental PCD. The role of autophagy in lace plant PCD was investigated using live cell imaging, transmission electron microscopy (TEM), immunolocalization, and in vivo pharmacological experimentation. ATG8 immunostaining and acridine orange staining revealed that autophagy occurs in both healthy and dying cells. Autophagosome-like vesicles were also found in healthy and dying cells through ultrastructural analysis with TEM. Following autophagy modulation, there was a noticeable increase in vesicles and vacuolar aggregates. A novel cell death assay utilizing lace plant leaves revealed that autophagy enhancement with rapamycin significantly decreased cell death rates compared to the control, whereas inhibition of autophagosome formation with wortmannin or blocking the degradation of cargoes with concanamycin A had an opposite effect. Although autophagy modulation significantly affected cell death rates in cells that are destined to die, neither the promotion nor inhibition of autophagy in whole plants had a significant effect on the number of perforations formed in lace plant leaves. Our data indicate that autophagy predominantly contributes to cell survival, and we found no clear evidence for its direct involvement in the induction of developmental PCD during perforation formation in lace plant leaves. |
format | Online Article Text |
id | pubmed-6817616 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-68176162019-11-06 The Function of Autophagy in Lace Plant Programmed Cell Death Dauphinee, Adrian N. Denbigh, Georgia L. Rollini, Alice Fraser, Meredith Lacroix, Christian R. Gunawardena, Arunika H. L. A. N. Front Plant Sci Plant Science The lace plant (Aponogeton madagascariensis) is an aquatic monocot that utilizes programmed cell death (PCD) to form perforations throughout its mature leaves as part of normal development. The lace plant is an emerging model system representing a unique form of developmental PCD. The role of autophagy in lace plant PCD was investigated using live cell imaging, transmission electron microscopy (TEM), immunolocalization, and in vivo pharmacological experimentation. ATG8 immunostaining and acridine orange staining revealed that autophagy occurs in both healthy and dying cells. Autophagosome-like vesicles were also found in healthy and dying cells through ultrastructural analysis with TEM. Following autophagy modulation, there was a noticeable increase in vesicles and vacuolar aggregates. A novel cell death assay utilizing lace plant leaves revealed that autophagy enhancement with rapamycin significantly decreased cell death rates compared to the control, whereas inhibition of autophagosome formation with wortmannin or blocking the degradation of cargoes with concanamycin A had an opposite effect. Although autophagy modulation significantly affected cell death rates in cells that are destined to die, neither the promotion nor inhibition of autophagy in whole plants had a significant effect on the number of perforations formed in lace plant leaves. Our data indicate that autophagy predominantly contributes to cell survival, and we found no clear evidence for its direct involvement in the induction of developmental PCD during perforation formation in lace plant leaves. Frontiers Media S.A. 2019-10-22 /pmc/articles/PMC6817616/ /pubmed/31695708 http://dx.doi.org/10.3389/fpls.2019.01198 Text en Copyright © 2019 Dauphinee, Denbigh, Rollini, Fraser, Lacroix and Gunawardena http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Plant Science Dauphinee, Adrian N. Denbigh, Georgia L. Rollini, Alice Fraser, Meredith Lacroix, Christian R. Gunawardena, Arunika H. L. A. N. The Function of Autophagy in Lace Plant Programmed Cell Death |
title | The Function of Autophagy in Lace Plant Programmed Cell Death |
title_full | The Function of Autophagy in Lace Plant Programmed Cell Death |
title_fullStr | The Function of Autophagy in Lace Plant Programmed Cell Death |
title_full_unstemmed | The Function of Autophagy in Lace Plant Programmed Cell Death |
title_short | The Function of Autophagy in Lace Plant Programmed Cell Death |
title_sort | function of autophagy in lace plant programmed cell death |
topic | Plant Science |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6817616/ https://www.ncbi.nlm.nih.gov/pubmed/31695708 http://dx.doi.org/10.3389/fpls.2019.01198 |
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