Physarum polycephalum macroplasmodium exhibits countermeasures against TiO 2 nanoparticle toxicity: A physiological, biochemical, transcriptional, and metabolic perspective
Concerns about the environmental and human health implications of TiO nanoparticles (nTiO ) are growing with their increased use in consumer and industrial products. Investigations of the underlying molecular mechanisms of nTiO tolerance in organisms will assist in countering nTiO toxicity. In this...
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Published in | Environmental pollution (1987) Vol. 279; p. 116936 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
Published |
England
15.06.2021
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Subjects | |
Online Access | Get full text |
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Summary: | Concerns about the environmental and human health implications of TiO
nanoparticles (nTiO
) are growing with their increased use in consumer and industrial products. Investigations of the underlying molecular mechanisms of nTiO
tolerance in organisms will assist in countering nTiO
toxicity. In this study, the countermeasures exhibited by the slime mold Physarum polycephalum macroplasmodium against nTiO
toxicity were investigated from a physiological, transcriptional, and metabolic perspective. The results suggested that the countermeasures against nTiO
exposure include gene-associated metabolic rearrangements in cellular pathways involved in amino acid, carbohydrate, and nucleic acid metabolism. Gene-associated nonmetabolic rearrangements involve processes such as DNA repair, DNA replication, and the cell cycle, and occur mainly when macroplasmodia are exposed to inhibitory doses of nTiO
. Interestingly, the growth of macroplasmodia and mammal cells was significantly restored by supplementation with a combination of responsive metabolites identified by metabolome analysis. Taken together, we report a novel model organism for the study of nTiO
tolerance and provide insights into countermeasures taken by macroplasmodia in response to nTiO
toxicity. Furthermore, we also present an approach to mitigate the effects of nTiO
toxicity in cells by metabolic intervention. |
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ISSN: | 1873-6424 |