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METACASPASE9 modulates autophagy to confine cell death to the target cells during Arabidopsis vascular xylem differentiation

We uncovered that the level of autophagy in plant cells undergoing programmed cell death determines the fate of the surrounding cells. Our approach consisted of using Arabidopsis thaliana cell cultures capable of differentiating into two different cell types: vascular tracheary elements (TEs) that u...

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Autores principales: Escamez, Sacha, André, Domenique, Zhang, Bo, Bollhöner, Benjamin, Pesquet, Edouard, Tuominen, Hannele
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Company of Biologists Ltd 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4823987/
https://www.ncbi.nlm.nih.gov/pubmed/26740571
http://dx.doi.org/10.1242/bio.015529
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author Escamez, Sacha
André, Domenique
Zhang, Bo
Bollhöner, Benjamin
Pesquet, Edouard
Tuominen, Hannele
author_facet Escamez, Sacha
André, Domenique
Zhang, Bo
Bollhöner, Benjamin
Pesquet, Edouard
Tuominen, Hannele
author_sort Escamez, Sacha
collection PubMed
description We uncovered that the level of autophagy in plant cells undergoing programmed cell death determines the fate of the surrounding cells. Our approach consisted of using Arabidopsis thaliana cell cultures capable of differentiating into two different cell types: vascular tracheary elements (TEs) that undergo programmed cell death (PCD) and protoplast autolysis, and parenchymatic non-TEs that remain alive. The TE cell type displayed higher levels of autophagy when expression of the TE-specific METACASPASE9 (MC9) was reduced using RNAi (MC9-RNAi). Misregulation of autophagy in the MC9-RNAi TEs coincided with ectopic death of the non-TEs, implying the existence of an autophagy-dependent intercellular signalling from within the TEs towards the non-TEs. Viability of the non-TEs was restored when AUTOPHAGY2 (ATG2) was downregulated specifically in MC9-RNAi TEs, demonstrating the importance of autophagy in the spatial confinement of cell death. Our results suggest that other eukaryotic cells undergoing PCD might also need to tightly regulate their level of autophagy to avoid detrimental consequences for the surrounding cells.
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spelling pubmed-48239872016-04-07 METACASPASE9 modulates autophagy to confine cell death to the target cells during Arabidopsis vascular xylem differentiation Escamez, Sacha André, Domenique Zhang, Bo Bollhöner, Benjamin Pesquet, Edouard Tuominen, Hannele Biol Open Research Article We uncovered that the level of autophagy in plant cells undergoing programmed cell death determines the fate of the surrounding cells. Our approach consisted of using Arabidopsis thaliana cell cultures capable of differentiating into two different cell types: vascular tracheary elements (TEs) that undergo programmed cell death (PCD) and protoplast autolysis, and parenchymatic non-TEs that remain alive. The TE cell type displayed higher levels of autophagy when expression of the TE-specific METACASPASE9 (MC9) was reduced using RNAi (MC9-RNAi). Misregulation of autophagy in the MC9-RNAi TEs coincided with ectopic death of the non-TEs, implying the existence of an autophagy-dependent intercellular signalling from within the TEs towards the non-TEs. Viability of the non-TEs was restored when AUTOPHAGY2 (ATG2) was downregulated specifically in MC9-RNAi TEs, demonstrating the importance of autophagy in the spatial confinement of cell death. Our results suggest that other eukaryotic cells undergoing PCD might also need to tightly regulate their level of autophagy to avoid detrimental consequences for the surrounding cells. The Company of Biologists Ltd 2016-01-06 /pmc/articles/PMC4823987/ /pubmed/26740571 http://dx.doi.org/10.1242/bio.015529 Text en © 2016. Published by The Company of Biologists Ltd http://creativecommons.org/licenses/by/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0), which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.
spellingShingle Research Article
Escamez, Sacha
André, Domenique
Zhang, Bo
Bollhöner, Benjamin
Pesquet, Edouard
Tuominen, Hannele
METACASPASE9 modulates autophagy to confine cell death to the target cells during Arabidopsis vascular xylem differentiation
title METACASPASE9 modulates autophagy to confine cell death to the target cells during Arabidopsis vascular xylem differentiation
title_full METACASPASE9 modulates autophagy to confine cell death to the target cells during Arabidopsis vascular xylem differentiation
title_fullStr METACASPASE9 modulates autophagy to confine cell death to the target cells during Arabidopsis vascular xylem differentiation
title_full_unstemmed METACASPASE9 modulates autophagy to confine cell death to the target cells during Arabidopsis vascular xylem differentiation
title_short METACASPASE9 modulates autophagy to confine cell death to the target cells during Arabidopsis vascular xylem differentiation
title_sort metacaspase9 modulates autophagy to confine cell death to the target cells during arabidopsis vascular xylem differentiation
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4823987/
https://www.ncbi.nlm.nih.gov/pubmed/26740571
http://dx.doi.org/10.1242/bio.015529
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