Online citations, reference lists, and bibliographies.

Programmed Cell Death Evidence In Wheat (Triticum Aestivum L.) Roots Induced By Aluminum Oxide (Al2O3) Nanoparticles

Fatma Yanik, Özlem Aytürk, Filiz Vardar
Published 2017 · Biology

Cite This
Download PDF
Analyze on Scholarcy
Share
Abstract Nanoparticles have been recognized as an abiotic stress factor in the last decade. Although they are extensively used in nanotechnology, the possible effects of nanoparticles on plants are still unclear. Therefore the aim of the present study was to determine the dose dependent effects of 13 nm-sized aluminum oxide nanoparticles (Al2O3 NPs) on wheat roots correlating with programmed cell death related characteristics. Exposure to different concentrations of Al2O3 NPs (5, 25 and 50 mg ml–1) decreased the mitotic indices dose dependently and caused chromosomal abnormalities such as c-mitosis, monopolar metaphase and stickiness after 96 h. Loss of plasma membrane integrity and irregular microtubule aggregations were determined. Nuclear deformations and TUNEL positive reactions indicating programmed cell death were also observed. Al2O3 NP-induced caspase 3, 8 and 9-like activities which control programmed cell death were observed in all concentrations. According to our results Al2O3 NPs induced programmed cell death in wheat roots after 96 h.
This paper references
Programmed cell death occurs asymmetrically during abscission in tomato
T Bar-Dror (2011)
10.1080/00087114.2006.10797935
Programmed cell death in the nucellus of Tillandsia (Bromeliaceae)
L. Brighigna (2006)
10.1007/s10725-010-9517-2
MEK/ERK inhibitor U0126 enhanced salt stress-induced programmed cell death in Thellungiella halophila suspension-cultured cells
J. Wang (2010)
10.1039/c5nr01448d
Titanium dioxide nanoparticles alter cellular morphology via disturbing the microtubule dynamics.
Zhilei Mao (2015)
Genotoxicity of Aluminum Oxide ($Al_2O_3$) Nanoparticle in Mammalian Cell Lines
Youn-Jung Kim (2009)
10.1023/A:1025548512438
Broader Societal Issues of Nanotechnology
M. Roco (2003)
10.1007/978-1-4684-0892-8_5
Plant Test Systems for Detection of Chemical Mutagens
R. Nilan (1976)
Aluminum induced caspase like activities in some Gramineae species
Aytürk Özlem (2015)
10.1016/j.wasman.2009.04.001
Nanoparticles: their potential toxicity, waste and environmental management.
G. Bystrzejewska-Piotrowska (2009)
The effects of nano-TiO 2 on seed germination, development and mitosis of root tip cells of Vicia narbonensis L. and Zea mays L
M Ruffini Castiglione (2011)
10.1080/00087114.2013.852342
Cytogenetic effects of chitosan-capped silver nanoparticles in the Allium cepa test
Dmitry S. Pesnya (2013)
10.1101/cshperspect.a008656
Caspase functions in cell death and disease.
D. Mcilwain (2013)
10.1007/BF00292840
Reverse fluorescent chromosome banding with chromomycin and DAPI
D. Schweizer (2004)
10.1007/S11051-010-0135-8
The effects of nano-TiO2 on seed germination, development and mitosis of root tip cells of Vicia narbonensis L. and Zea mays L
M. Ruffini Castiglione (2010)
INHIBITION OF BARLEY ROOT GROWTH BY ACTINOMYCIN D: EFFECTS ON MITOTIC ACTIVITY, PROTEIN CONTENT AND PEROXIDASE ACTIVITY
F. Vardar (2007)
10.1038/cdd.2009.59
Caspase activation pathways: some recent progress
S. Cullen (2009)
10.15835/NBHA3915865
Immunolocalization of Lipoxygenase in the Anther Wall Cells of Lathyrus undulatus Boiss. during Programmed Cell Death
F. Vardar (2011)
10.1016/J.FLORA.2009.02.001
The ultrastructure of the development of Tillandsia (Bromeliaceae) trichome
Alessio Papini (2010)
10.1016/S1937-6448(08)01403-2
Programmed cell death in plants: new insights into redox regulation and the role of hydrogen peroxide.
Ilya Gadjev (2008)
Do plant caspases exist? Plant Physiol
EJ Woltering (2002)
10.1093/PCP/PCE091
Fate of nascent microtubules organized at the M/G1 interface, as visualized by synchronized tobacco BY-2 cells stably expressing GFP-tubulin: time-sequence observations of the reorganization of cortical microtubules in living plant cells.
F. Kumagai (2001)
10.1080/00087114.2016.1139416
In vitro and in vivo genotoxicity and molecular response of silver nanoparticles on different biological model systems
S. Sobieh (2016)
10.1104/pp.006338
Do Plant Caspases Exist?
E. Woltering (2002)
10.1016/j.jhazmat.2009.12.089
Comparative study of the cytotoxic and genotoxic effects of titanium oxide and aluminium oxide nanoparticles in Chinese hamster ovary (CHO-K1) cells.
A. L. Di Virgilio (2010)
Proteolytic Enzymes in Plant Programmed Cell Death
F. Vardar (2008)
10.1016/S0070-2153(05)71007-3
Cell death and organ development in plants.
H. Rogers (2005)
10.1016/J.PLANTSCI.2004.07.021
Oxidative stress in Arabidopsis thaliana exposed to cadmium is due to hydrogen peroxide accumulation
U. Cho (2005)
10.1007/s00709-014-0649-5
Impact of TiO2 nanoparticles on Vicia narbonensis L.: potential toxicity effects
Monica Ruffini Castiglione (2014)
10.2105/AJPH.62.8.1153
Chemical mutagens: principles and methods for their detection.
Robert L. Elston (1972)
10.3109/17435390.2014.969791
Amorphous silica nanoparticles alter microtubule dynamics and cell migration
Laetitia Gonzalez (2015)
10.1074/jbc.M603487200
Loss of Caspase-9 Provides Genetic Evidence for the Type I/II Concept of CD95-mediated Apoptosis*
A. K. Samraj (2006)
10.1556/ABiol.63.2012.1.5
Ultrastructural aspects and programmed cell death in the tapetal cells of Lathyrus undulatus Boiss.
Filiz Vardar (2012)
10.1155/2012/751686
Environmental Nanoparticles Interactions with Plants: Morphological, Physiological, and Genotoxic Aspects
Christy Remedios (2012)
Broader societal issue of nanotechnology
Roco MC. (2003)
10.1007/s10646-013-1058-9
Salicylic acid alleviates aluminum toxicity in rice seedlings better than magnesium and calcium by reducing aluminum uptake, suppressing oxidative damage and increasing antioxidative defense
Poonam Pandey (2013)
Accumulation of Aluminium by Plants Exposed to Nano- and Microsized Particles of Al 2 O 3
M. Asztemborska (2015)
10.1094/MPMI-11-11-0283-R
TaMCA4, a novel wheat metacaspase gene functions in programmed cell death induced by the fungal pathogen Puccinia striiformis f. sp. tritici.
X. Wang (2012)
10.1093/JXB/ERM189
Programmed cell death and tissue remodelling in plants.
A. Gunawardena (2008)
Nanotechnology and agroecosystem.
C. R. Chinnamuthu (2009)
10.1016/J.PLANTSCI.2006.11.002
Caspase-like proteases involvement in programmed cell death of Phaseolus coccineus suspensor
L. Lombardi (2007)
10.1007/s00425-010-1304-9
Environmentally induced programmed cell death in leaf protoplasts of Aponogeton madagascariensis
Christina E. N. Lord (2011)
10.1105/tpc.8.3.375
Apoptosis: A Functional Paradigm for Programmed Plant Cell Death Induced by a Host-Selective Phytotoxin and Invoked during Development.
H. Wang (1996)
10.1126/SCIENCE.1114397
Toxic Potential of Materials at the Nanolevel
A. Nel (2006)
10.1016/J.ENVEXPBOT.2013.03.002
Toxicity of aluminium oxide nanoparticles demonstrated using a BY-2 plant cell suspension culture model
Zuzana Poborilova (2013)
10.3390/ma3063468
Polymer-Nanoparticle Composites: From Synthesis to Modern Applications
T. Hanemann (2010)
10.22059/IJER.2015.880
Accumulation ofAluminiumby Plants Exposed toNano- andMicrosized Particles of Al2O3
M. Asztemborska (2015)
10.1007/s11738-007-0086-6
Caspase-like proteases and their role in programmed cell death in plants
E. Piszczek (2007)
Genotoxicity of aluminium oxide (Al 2 O 3 ) nanoparticle in mammalian cell lines
Y J Kim (2009)
10.1073/pnas.93.22.12094
Programmed cell death: a way of life for plants.
J. Greenberg (1996)
10.1073/pnas.072544399
Oligomerization and activation of caspase-9, induced by Apaf-1 CARD
E. Shiozaki (2002)
10.1007/s00709-010-0221-x
Megasporogenesis and programmed cell death in Tillandsia (Bromeliaceae)
Alessio Papini (2010)
10.1016/S0962-8924(99)01584-6
When cells die
A. Bergmann (2000)
10.9787/PBB.2013.1.2.148
Identification and expression analysis of wheat vacuolar processing enzymes (VPEs).
Tae Hoon Kang (2013)
10.1023/A:1026532223173
Programmed cell death of tracheary elements as a paradigm in plants
H. Fukuda (2004)
10.1002/BIES.20493
Reactive oxygen species as signals that modulate plant stress responses and programmed cell death
T. Gechev (2006)
10.1093/OXFORDJOURNALS.PCP.A029455
Evidence for Programmed Cell Death during Leaf Senescence in Plants
C. Yen (1998)
10.1016/s0960-9822(07)00555-6
Caspases and programmed cell death in the hypersensitive response of plants to pathogens
Olga María del Pozo (1998)
10.1021/es202995d
Toxicity, Uptake, and Translocation of Engineered Nanomaterials in Vascular plants.
P. Miralles (2012)
10.1007/s11270-015-2566-4
Toxic Effects of Aluminum Oxide (Al2O3) Nanoparticles on Root Growth and Development in Triticum aestivum
F. Yanik (2015)
10.1038/nrm1496
Molecular mechanisms of caspase regulation during apoptosis
S. Riedl (2004)
10.1007/s00709-016-0969-8
Female gametophyte and embryo development in Helleborus bocconei Ten. (Ranunculaceae)
G. Bartoli (2016)
10.3390/ijms14011608
UV-Induced Cell Death in Plants
Ganesh M Nawkar (2013)
10.1080/00087114.2015.1109954
Determination of aluminum induced programmed cell death characterized by DNA fragmentation in Gramineae species
F. Vardar (2016)



This paper is referenced by
Semantic Scholar Logo Some data provided by SemanticScholar