The Function of Autophagy in Lace Plant Programmed Cell Death

Adrian N. Dauphinee, Georgia L. Denbigh, Alice Rollini, Meredith Fraser, Christian R. Lacroix, Arunika H.L.A.N. Gunawardena

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14 Citations (Scopus)

Abstract

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.

Original languageEnglish
Article number1198
JournalFrontiers in Plant Science
Volume10
DOIs
Publication statusPublished - Oct 22 2019

Bibliographical note

Funding Information:
We thank Dr. Joanna Kacprzyk (University College Dublin) for a critical review of this manuscript and The Killam Trusts and the Natural Sciences and Engineering Research Council (NSERC) of Canada for providing PhD funding to AD. Later, AD was supported by AG’s NSERC Discovery accelerator

Funding Information:
This work was supported by AG’s NSERC Discovery Grant (# 2017-04299) and Accelerator Supplements (# 2017-507825).

Funding Information:
We thank Dr. Joanna Kacprzyk (University College Dublin) for a critical review of this manuscript and The Killam Trusts and the Natural Sciences and Engineering Research Council (NSERC) of Canada for providing PhD funding to AD. Later, AD was supported by AG?s NSERC Discovery accelerator supplements (DAS) as a postdoctoral. GD was supported by a Nova Scotia Research and Innovation Graduate Scholarship and AG?s NSERC discovery grant. MF was supported by NSERC and Sarah Lawson Research Scholarships. Stephen Chew assisted with optimization of the live cell imaging assay and was supported by a Sarah Lawson Research Scholarship. We also thank Mary Ann Trevors (Dalhousie Facilities) for assistance with TEM including sample preparations.

Publisher Copyright:
© Copyright © 2019 Dauphinee, Denbigh, Rollini, Fraser, Lacroix and Gunawardena.

ASJC Scopus Subject Areas

  • Plant Science

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