scholarly journals Carbon nanotube biocompatibility in plants is determined by their surface chemistry

2021 ◽  
Vol 19 (1) ◽  
Author(s):  
Eduardo González-Grandío ◽  
Gözde S. Demirer ◽  
Christopher T. Jackson ◽  
Darwin Yang ◽  
Sophia Ebert ◽  
...  

Abstract Background Agriculture faces significant global challenges including climate change and an increasing food demand due to a growing population. Addressing these challenges will require the adoption of transformative innovations into biotechnology practice, such as nanotechnology. Recently, nanomaterials have emerged as unmatched tools for their use as biosensors, or as biomolecule delivery vehicles. Despite their increasingly prolific use, plant-nanomaterial interactions remain poorly characterized, drawing into question the breadth of their utility and their broader environmental compatibility. Results Herein, we characterize the response of Arabidopsis thaliana to single walled carbon nanotube (SWNT) exposure with two different surface chemistries commonly used for biosensing and nucleic acid delivery: oligonucleotide adsorbed-pristine SWNTs, and polyethyleneimine-SWNTs loaded with plasmid DNA (PEI-SWNTs), both introduced by leaf infiltration. We observed that pristine SWNTs elicit a mild stress response almost undistinguishable from the infiltration process, indicating that these nanomaterials are well-tolerated by the plant. However, PEI-SWNTs induce a much larger transcriptional reprogramming that involves stress, immunity, and senescence responses. PEI-SWNT-induced transcriptional profile is very similar to that of mutant plants displaying a constitutive immune response or treated with stress-priming agrochemicals. We selected molecular markers from our transcriptomic analysis and identified PEI as the main cause of this adverse reaction. We show that PEI-SWNT response is concentration-dependent and, when persistent over time, leads to cell death. We probed a panel of PEI variant-functionalized SWNTs across two plant species and identified biocompatible SWNT surface functionalizations. Conclusions While SWNTs themselves are well tolerated by plants, SWNTs surface-functionalized with positively charged polymers become toxic and produce cell death. We use molecular markers to identify more biocompatible SWNT formulations. Our results highlight the importance of nanoparticle surface chemistry on their biocompatibility and will facilitate the use of functionalized nanomaterials for agricultural improvement. Graphical Abstract

2021 ◽  
Author(s):  
Eduardo González-Grandío ◽  
Gözde Sultan Demirer ◽  
Christopher Tonnu Jackson ◽  
Darwin Yang ◽  
Markita P Landry

Agriculture faces significant global challenges including climate change and an increasing food demand due to a growing population. Addressing these challenges will require the adoption of transformative innovations into biotechnology practice, such as nanotechnology. Recently, nanomaterials have emerged as unmatched tools for their use as biosensors, or as biomolecule delivery vehicles. Despite their increasingly prolific use, plant-nanomaterial interactions remain poorly characterized, drawing into question the breadth of their utility and their broader environmental compatibility. Herein, we characterize Arabidopsis thaliana transcriptional response to single walled carbon nanotubes (SWNTs) with two different surface chemistries commonly used for biosensing and nucleic acid delivery: oligonucleotide adsorbed-pristine SWNTs, and polyethyleneimine-SWNTs loaded with plasmid DNA (PEI-SWNTs), both introduced by leaf infiltration. We observed that SWNTs elicit a mild stress response almost undistinguishable from the infiltration process, indicating that these nanomaterials are well-tolerated by the plant. However, PEI-SWNTs induce a much larger transcriptional reprogramming that involves stress, immunity, and senescence responses. PEI-SWNT-induced transcriptional profile is very similar to that of mutant plants displaying a constitutive immune response or treated with stress-priming agrochemicals. We selected molecular markers from our transcriptomic analysis and identified PEI as the main cause of this reaction. We show that PEI-SWNT response is concentration-dependent and, when persistent over time, leads to cell death. We probed a panel of PEI variant-functionalized SWNTs across two plant species and identified biocompatible SWNT surface functionalizations. Our results highlight the importance of nanoparticle surface chemistry on their biocompatibility and will facilitate the use of functionalized nanomaterials for agricultural improvement.


Author(s):  
Krissia Franco de Godoy ◽  
Joice Margareth de Almeida Rodolpho ◽  
Patrícia Brassolatti ◽  
Bruna Dias de Lima Fragelli ◽  
Cynthia Aparecida de Castro ◽  
...  

2017 ◽  
Vol 9 (7) ◽  
pp. 6512-6519 ◽  
Author(s):  
Yu Zhang ◽  
Mena R. Klittich ◽  
Min Gao ◽  
Ali Dhinojwala

Langmuir ◽  
2008 ◽  
Vol 24 (22) ◽  
pp. 13173-13181 ◽  
Author(s):  
Thomas Crouzier ◽  
Aditya Nimmagadda ◽  
Matthias U. Nollert ◽  
Peter S. McFetridge

2012 ◽  
Vol 23 (37) ◽  
pp. 375102 ◽  
Author(s):  
Ilknur Sur ◽  
Mine Altunbek ◽  
Mehmet Kahraman ◽  
Mustafa Culha

2021 ◽  
Author(s):  
In Jun Yeo ◽  
Ji Eun Yu ◽  
Sung Sik Yoo ◽  
Jaesuk Yun ◽  
Dong Ju Son ◽  
...  

Abstract Extensive epidemiological evidence indicates that patients with certain cancers have a lower probability of developing some types of neurodegenerative diseases (ND) and mood disorders and vice versa. These inverse comorbidities may be associated with several different molecular processes. p53, is a potentially responsible for regulating the development of ND, mood disorders as well as cancers. To investigate whether the tumor suppressor p53 may be associated with ND development, we studied the behavioral changes in p53 knockout (p53−/−) mice and possible action mechanisms. Increased anxiety-like but not depression-like behaviors were displayed in p53−/− mice without impaired motor activities under the non-chronic unpredictable mild stress condition. However, in the p53−/− mice, more anxiety-like and depression-like behaviors were observed in the chronic unpredictable mild stress (CUMS) condition. Our mechanism studies showed that brain-derived neurotrophic factor (BDNF) protein was significantly downregulated, but glutamate levels were significantly increased in the prefrontal cortex of p53−/− mice. Further analyses showed that the p53−/− mice caused more stress-induced nerve damage as a result of an increase in intracellular calcium levels and N-methyl D-aspartate receptor subtype 2B (NMDAR2B) expression. Treatment with corticosterone (mimics CUMS in vitro) increased glutamate levels, NMDAR2B expression, and calcium levels, and these levels were elevated by co-treatment with pifithrin-α (p53 inhibitor) in PC12 cells. Cell death and cell death-mediated signals (p-p38, p-JNK and caspase-3) were upregulated, but neuroprotective signals (BDNF p-Akt, p-ERK and p-CREB) were downregulated in p53−/− mice, and corticoid and/or pifithrin-α treated PC12 cells. These data indicate that p53 may be an important preventive factor against depression and anxiety, and thus suggests a possible correlation between cancer and anxiety/depression development. Running title: Deficiency of p53 enhances mental disorder


Oncotarget ◽  
2016 ◽  
Vol 7 (31) ◽  
pp. 49539-49551 ◽  
Author(s):  
Sonja C. Lueck ◽  
Annika C. Russ ◽  
Ursula Botzenhardt ◽  
Richard F. Schlenk ◽  
Kerry Zobel ◽  
...  

2011 ◽  
Vol 184 (3) ◽  
pp. 655-666 ◽  
Author(s):  
F. Marquez-Linares ◽  
O.N.C. Uwakweh ◽  
N. Lopez ◽  
E. Chavez ◽  
R. Polanco ◽  
...  

1998 ◽  
Vol 142 (4) ◽  
pp. 1135-1144 ◽  
Author(s):  
Maria Nurminskaya ◽  
Cordula Magee ◽  
Dmitry Nurminsky ◽  
Thomas F. Linsenmayer

We previously used subtractive hybridization to isolate cDNAs for genes upregulated in chick hypertrophic chondrocytes (Nurminskaya, M., and T.F. Linsenmayer. 1996. Dev. Dyn. 206:260–271). Certain of these showed homology with the “A” subunit of human plasma transglutaminase (factor XIIIA), a member of a family of enzymes that cross-link a variety of intracellular and matrix molecules. We now have isolated a full-length cDNA for this molecule, and confirmed that it is avian factor XIIIA. Northern and enzymatic analyses confirm that the molecule is upregulated in hypertrophic chondrocytes (as much as eightfold). The enzymatic analyses also show that appreciable transglutaminase activity in the hypertrophic zone becomes externalized into the extracellular matrix. This externalization most likely is effected by cell death and subsequent lysis—effected by the transglutaminase itself. When hypertrophic chondrocytes are transfected with a cDNA construct encoding the zymogen of factor XIIIA, the cells convert the translated protein to a lower molecular weight form, and they initiate cell death, become permeable to macromolecules and eventually undergo lysis. Non-hypertrophic cells transfected with the same construct do not show these degenerative changes. These results suggest that hypertrophic chondrocytes have a novel, tissue-specific cascade of mechanisms that upregulate the synthesis of plasma transglutaminase and activate its zymogen. This produces autocatalytic cell death, externalization of the enzyme, and presumably cross-linking of components within the hypertrophic matrix. These changes may in turn regulate the removal and/or calcification of this hypertrophic matrix, which are its ultimate fates.


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