Cargando…
ATP depletion plays a pivotal role in self‐incompatibility, revealing a link between cellular energy status, cytosolic acidification and actin remodelling in pollen tubes
Self‐incompatibility (SI) involves specific interactions during pollination to reject incompatible (‘self’) pollen, preventing inbreeding in angiosperms. A key event observed in pollen undergoing the Papaver rhoeas SI response is the formation of punctate F‐actin foci. Pollen tube growth is heavily...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9796540/ https://www.ncbi.nlm.nih.gov/pubmed/35775998 http://dx.doi.org/10.1111/nph.18350 |
_version_ | 1784860509798924288 |
---|---|
author | Wang, Ludi Lin, Zongcheng Carli, José Gladala‐Kostarz, Agnieszka Davies, Julia M. Franklin‐Tong, Vernonica E. Bosch, Maurice |
author_facet | Wang, Ludi Lin, Zongcheng Carli, José Gladala‐Kostarz, Agnieszka Davies, Julia M. Franklin‐Tong, Vernonica E. Bosch, Maurice |
author_sort | Wang, Ludi |
collection | PubMed |
description | Self‐incompatibility (SI) involves specific interactions during pollination to reject incompatible (‘self’) pollen, preventing inbreeding in angiosperms. A key event observed in pollen undergoing the Papaver rhoeas SI response is the formation of punctate F‐actin foci. Pollen tube growth is heavily energy‐dependent, yet ATP levels in pollen tubes have not been directly measured during SI. Here we used transgenic Arabidopsis lines expressing the Papaver pollen S‐determinant to investigate a possible link between ATP levels, cytosolic pH ([pH](cyt)) and alterations to the actin cytoskeleton. We identify for the first time that SI triggers a rapid and significant ATP depletion in pollen tubes. Artificial depletion of ATP triggered cytosolic acidification and formation of actin aggregates. We also identify in vivo, evidence for a threshold [pH](cyt) of 5.8 for actin foci formation. Imaging revealed that SI stimulates acidic cytosolic patches adjacent to the plasma membrane. In conclusion, this study provides evidence that ATP depletion plays a pivotal role in SI upstream of programmed cell death and reveals a link between the cellular energy status, cytosolic acidification and alterations to the actin cytoskeleton in regulating Papaver SI in pollen tubes. |
format | Online Article Text |
id | pubmed-9796540 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-97965402022-12-30 ATP depletion plays a pivotal role in self‐incompatibility, revealing a link between cellular energy status, cytosolic acidification and actin remodelling in pollen tubes Wang, Ludi Lin, Zongcheng Carli, José Gladala‐Kostarz, Agnieszka Davies, Julia M. Franklin‐Tong, Vernonica E. Bosch, Maurice New Phytol Research Self‐incompatibility (SI) involves specific interactions during pollination to reject incompatible (‘self’) pollen, preventing inbreeding in angiosperms. A key event observed in pollen undergoing the Papaver rhoeas SI response is the formation of punctate F‐actin foci. Pollen tube growth is heavily energy‐dependent, yet ATP levels in pollen tubes have not been directly measured during SI. Here we used transgenic Arabidopsis lines expressing the Papaver pollen S‐determinant to investigate a possible link between ATP levels, cytosolic pH ([pH](cyt)) and alterations to the actin cytoskeleton. We identify for the first time that SI triggers a rapid and significant ATP depletion in pollen tubes. Artificial depletion of ATP triggered cytosolic acidification and formation of actin aggregates. We also identify in vivo, evidence for a threshold [pH](cyt) of 5.8 for actin foci formation. Imaging revealed that SI stimulates acidic cytosolic patches adjacent to the plasma membrane. In conclusion, this study provides evidence that ATP depletion plays a pivotal role in SI upstream of programmed cell death and reveals a link between the cellular energy status, cytosolic acidification and alterations to the actin cytoskeleton in regulating Papaver SI in pollen tubes. John Wiley and Sons Inc. 2022-07-23 2022-12 /pmc/articles/PMC9796540/ /pubmed/35775998 http://dx.doi.org/10.1111/nph.18350 Text en © 2022 The Authors. New Phytologist © 2022 New Phytologist Foundation. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Wang, Ludi Lin, Zongcheng Carli, José Gladala‐Kostarz, Agnieszka Davies, Julia M. Franklin‐Tong, Vernonica E. Bosch, Maurice ATP depletion plays a pivotal role in self‐incompatibility, revealing a link between cellular energy status, cytosolic acidification and actin remodelling in pollen tubes |
title | ATP depletion plays a pivotal role in self‐incompatibility, revealing a link between cellular energy status, cytosolic acidification and actin remodelling in pollen tubes |
title_full | ATP depletion plays a pivotal role in self‐incompatibility, revealing a link between cellular energy status, cytosolic acidification and actin remodelling in pollen tubes |
title_fullStr | ATP depletion plays a pivotal role in self‐incompatibility, revealing a link between cellular energy status, cytosolic acidification and actin remodelling in pollen tubes |
title_full_unstemmed | ATP depletion plays a pivotal role in self‐incompatibility, revealing a link between cellular energy status, cytosolic acidification and actin remodelling in pollen tubes |
title_short | ATP depletion plays a pivotal role in self‐incompatibility, revealing a link between cellular energy status, cytosolic acidification and actin remodelling in pollen tubes |
title_sort | atp depletion plays a pivotal role in self‐incompatibility, revealing a link between cellular energy status, cytosolic acidification and actin remodelling in pollen tubes |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9796540/ https://www.ncbi.nlm.nih.gov/pubmed/35775998 http://dx.doi.org/10.1111/nph.18350 |
work_keys_str_mv | AT wangludi atpdepletionplaysapivotalroleinselfincompatibilityrevealingalinkbetweencellularenergystatuscytosolicacidificationandactinremodellinginpollentubes AT linzongcheng atpdepletionplaysapivotalroleinselfincompatibilityrevealingalinkbetweencellularenergystatuscytosolicacidificationandactinremodellinginpollentubes AT carlijose atpdepletionplaysapivotalroleinselfincompatibilityrevealingalinkbetweencellularenergystatuscytosolicacidificationandactinremodellinginpollentubes AT gladalakostarzagnieszka atpdepletionplaysapivotalroleinselfincompatibilityrevealingalinkbetweencellularenergystatuscytosolicacidificationandactinremodellinginpollentubes AT daviesjuliam atpdepletionplaysapivotalroleinselfincompatibilityrevealingalinkbetweencellularenergystatuscytosolicacidificationandactinremodellinginpollentubes AT franklintongvernonicae atpdepletionplaysapivotalroleinselfincompatibilityrevealingalinkbetweencellularenergystatuscytosolicacidificationandactinremodellinginpollentubes AT boschmaurice atpdepletionplaysapivotalroleinselfincompatibilityrevealingalinkbetweencellularenergystatuscytosolicacidificationandactinremodellinginpollentubes |