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Optical Visualization of Red-GQDs’ Organelles Distribution and Localization in Living Cells

Recently, there has been a rapidly expanding interest in a new nanomaterial, graphene quantum dots (GQDs), owing to its profound potential in various advanced applications. At present, the study of GQDs mainly focuses on the new synthesis methods and surface modification. However, revealing the intr...

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Autores principales: Hu, Haifeng, Li, Peng, Qiu, Jie, Zhao, Meiji, Kuang, Mingjie, Zhang, Zhaoyan, Wang, Dachuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9326348/
https://www.ncbi.nlm.nih.gov/pubmed/35910373
http://dx.doi.org/10.3389/fphar.2022.932807
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author Hu, Haifeng
Li, Peng
Qiu, Jie
Zhao, Meiji
Kuang, Mingjie
Zhang, Zhaoyan
Wang, Dachuan
author_facet Hu, Haifeng
Li, Peng
Qiu, Jie
Zhao, Meiji
Kuang, Mingjie
Zhang, Zhaoyan
Wang, Dachuan
author_sort Hu, Haifeng
collection PubMed
description Recently, there has been a rapidly expanding interest in a new nanomaterial, graphene quantum dots (GQDs), owing to its profound potential in various advanced applications. At present, the study of GQDs mainly focuses on the new synthesis methods and surface modification. However, revealing the intracellular distribution of GQDs is currently not available, limiting in-depth understanding of its biological regulatory mechanism. To fill up this gap, the visualization study of red fluorescent graphene quantum dots (Red-GQDs) is helpful to clarify their subcellular distribution and metabolism in living cells system. Here, in this study, two-photon laser confocal microscopy was used to deeply analyze the uptake and subcellular distribution of Red-GQDs by HeLa cells at different concentrations and times through visual observation and discussed the effect of Red-GQDs on the metabolic of HeLa cells. The results indicated that Red-GQDs could be well-absorbed by HeLa cells and further revealed the differential distribution of Red-GQDs in different organelles (lysosomes and mitochondria) in a time-dependent manner. In addition, we confirmed that Red-GQDs significantly affect cell biological functions. Low concentrations of Red-GQDs are related to the autophagy pathway of cells, and high concentrations of Red-GQDs can induce ferroptosis in cells and promote the secretion of cellular exosomes. In the present study, the distribution and metabolic pathways of Red-GQDs in the subcellular structure of cells were characterized in detail through visual analysis, which can bring positive reference for the application of Red-GQDs in the future.
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spelling pubmed-93263482022-07-28 Optical Visualization of Red-GQDs’ Organelles Distribution and Localization in Living Cells Hu, Haifeng Li, Peng Qiu, Jie Zhao, Meiji Kuang, Mingjie Zhang, Zhaoyan Wang, Dachuan Front Pharmacol Pharmacology Recently, there has been a rapidly expanding interest in a new nanomaterial, graphene quantum dots (GQDs), owing to its profound potential in various advanced applications. At present, the study of GQDs mainly focuses on the new synthesis methods and surface modification. However, revealing the intracellular distribution of GQDs is currently not available, limiting in-depth understanding of its biological regulatory mechanism. To fill up this gap, the visualization study of red fluorescent graphene quantum dots (Red-GQDs) is helpful to clarify their subcellular distribution and metabolism in living cells system. Here, in this study, two-photon laser confocal microscopy was used to deeply analyze the uptake and subcellular distribution of Red-GQDs by HeLa cells at different concentrations and times through visual observation and discussed the effect of Red-GQDs on the metabolic of HeLa cells. The results indicated that Red-GQDs could be well-absorbed by HeLa cells and further revealed the differential distribution of Red-GQDs in different organelles (lysosomes and mitochondria) in a time-dependent manner. In addition, we confirmed that Red-GQDs significantly affect cell biological functions. Low concentrations of Red-GQDs are related to the autophagy pathway of cells, and high concentrations of Red-GQDs can induce ferroptosis in cells and promote the secretion of cellular exosomes. In the present study, the distribution and metabolic pathways of Red-GQDs in the subcellular structure of cells were characterized in detail through visual analysis, which can bring positive reference for the application of Red-GQDs in the future. Frontiers Media S.A. 2022-07-13 /pmc/articles/PMC9326348/ /pubmed/35910373 http://dx.doi.org/10.3389/fphar.2022.932807 Text en Copyright © 2022 Hu, Li, Qiu, Zhao, Kuang, Zhang and Wang. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pharmacology
Hu, Haifeng
Li, Peng
Qiu, Jie
Zhao, Meiji
Kuang, Mingjie
Zhang, Zhaoyan
Wang, Dachuan
Optical Visualization of Red-GQDs’ Organelles Distribution and Localization in Living Cells
title Optical Visualization of Red-GQDs’ Organelles Distribution and Localization in Living Cells
title_full Optical Visualization of Red-GQDs’ Organelles Distribution and Localization in Living Cells
title_fullStr Optical Visualization of Red-GQDs’ Organelles Distribution and Localization in Living Cells
title_full_unstemmed Optical Visualization of Red-GQDs’ Organelles Distribution and Localization in Living Cells
title_short Optical Visualization of Red-GQDs’ Organelles Distribution and Localization in Living Cells
title_sort optical visualization of red-gqds’ organelles distribution and localization in living cells
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9326348/
https://www.ncbi.nlm.nih.gov/pubmed/35910373
http://dx.doi.org/10.3389/fphar.2022.932807
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