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Graphene Oxide Nanoparticels Interaction with Jurkat Cell Line in Cell-IQ System
S A Zamorina1, P V Khramtsov2, M B Rayev2
1Institute of Ecology and Genetics of Microorganisms, UB RAS Branch of the Perm Federal Research Center, Ural Branch of the Russian Academy of Sciences, Perm, Russia. zamorina.sa@gmail.com.
Doklady. Biochemistry and Biophysics
|December 30, 2021
Summary
Graphene oxide (GO) nanoparticles, coated with polyethylene glycol (PEG), were found to significantly reduce the proliferation and viability of Jurkat T cells. This study highlights potential cytotoxic effects of PEG-GO nanoparticles on lymphocytes.
Area of Science:
- Biomedical materials science
- Nanotechnology in medicine
- Cell biology
Background:
- Graphene oxide (GO) is a promising material for biomedical applications.
- Understanding the interaction of GO nanoparticles with specific cell types is crucial for safe clinical translation.
- Jurkat T cells are a relevant model for studying immune cell responses.
Purpose of the Study:
- To investigate the effect of polyethylene glycol (PEG)-coated graphene oxide (GO) nanoparticles on the proliferation and viability of Jurkat T cells.
- To assess the impact of nanoparticle size and concentration on cellular response.
- To evaluate the cytotoxic potential of PEG-GO nanoparticles in an in vitro setting.
Main Methods:
- Utilized the Cell-IQ system for intravital observation of Jurkat T cells.
- Exposed cells to GO nanoparticles of varying sizes coated with linear or branched PEG.
- Tested nanoparticle concentrations of 5 and 25 μg/mL over a 24-hour period.
Main Results:
- Direct contact with PEG-coated GO nanoparticles reduced cell mass growth by over twofold.
- A decrease of 5-9% in live Jurkat T cells was observed after 24 hours of exposure.
- These effects were consistent across different nanoparticle sizes and concentrations.
Conclusions:
- PEG-coated GO nanoparticles exhibit suppressive effects on Jurkat T lymphocyte proliferation and viability.
- The findings indicate potential cytotoxic properties of these nanomaterials on immune cells.
- Further research is warranted to elucidate the mechanisms of GO-nanoparticle-induced cytotoxicity.

