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Gold Nanoparticles and Graphene Oxide Flakes Enhance Cancer Cells’ Phagocytosis through Granzyme-Perforin-Dependent Biomechanism
The study aimed to investigate the roles of gold nanoparticles (GNPs) and graphene oxide flakes (GOFs) as phagocytosis enhancers against cancer cells. The nanomaterials were characterized through SEM and UV-VIS absorptions. The GNPs and GOFs increased the macrophages’ phagocytosis ability in engulfi...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8225074/ https://www.ncbi.nlm.nih.gov/pubmed/34073808 http://dx.doi.org/10.3390/nano11061382 |
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author | Al-Omar, Mohsen S. Jabir, Majid Karsh, Esraa Kadhim, Rua Sulaiman, Ghassan M. Taqi, Zainab J. Khashan, Khawla S. Mohammed, Hamdoon A. Khan, Riaz A. Mohammed, Salman A. A. |
author_facet | Al-Omar, Mohsen S. Jabir, Majid Karsh, Esraa Kadhim, Rua Sulaiman, Ghassan M. Taqi, Zainab J. Khashan, Khawla S. Mohammed, Hamdoon A. Khan, Riaz A. Mohammed, Salman A. A. |
author_sort | Al-Omar, Mohsen S. |
collection | PubMed |
description | The study aimed to investigate the roles of gold nanoparticles (GNPs) and graphene oxide flakes (GOFs) as phagocytosis enhancers against cancer cells. The nanomaterials were characterized through SEM and UV-VIS absorptions. The GNPs and GOFs increased the macrophages’ phagocytosis ability in engulfing, thereby annihilating the cancer cells in both in vitro and in vivo conditions. The GNPs and GOFs augmented serine protease class apoptotic protein, granzyme, passing through the aquaporin class protein, perforin, with mediated delivery through the cell membrane site for the programmed, calibrated, and conditioned cancer cells killing. Additionally, protease inhibitor 3,4-dichloroisocoumarin (DCI) significantly reduced granzyme and perforin activities of macrophages. The results demonstrated that the GOFs and GNPs increased the activation of phagocytic cells as a promising strategy for controlling cancer cells by augmenting the cell mortality through the granzyme-perforin-dependent mechanism. |
format | Online Article Text |
id | pubmed-8225074 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-82250742021-06-25 Gold Nanoparticles and Graphene Oxide Flakes Enhance Cancer Cells’ Phagocytosis through Granzyme-Perforin-Dependent Biomechanism Al-Omar, Mohsen S. Jabir, Majid Karsh, Esraa Kadhim, Rua Sulaiman, Ghassan M. Taqi, Zainab J. Khashan, Khawla S. Mohammed, Hamdoon A. Khan, Riaz A. Mohammed, Salman A. A. Nanomaterials (Basel) Article The study aimed to investigate the roles of gold nanoparticles (GNPs) and graphene oxide flakes (GOFs) as phagocytosis enhancers against cancer cells. The nanomaterials were characterized through SEM and UV-VIS absorptions. The GNPs and GOFs increased the macrophages’ phagocytosis ability in engulfing, thereby annihilating the cancer cells in both in vitro and in vivo conditions. The GNPs and GOFs augmented serine protease class apoptotic protein, granzyme, passing through the aquaporin class protein, perforin, with mediated delivery through the cell membrane site for the programmed, calibrated, and conditioned cancer cells killing. Additionally, protease inhibitor 3,4-dichloroisocoumarin (DCI) significantly reduced granzyme and perforin activities of macrophages. The results demonstrated that the GOFs and GNPs increased the activation of phagocytic cells as a promising strategy for controlling cancer cells by augmenting the cell mortality through the granzyme-perforin-dependent mechanism. MDPI 2021-05-24 /pmc/articles/PMC8225074/ /pubmed/34073808 http://dx.doi.org/10.3390/nano11061382 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Al-Omar, Mohsen S. Jabir, Majid Karsh, Esraa Kadhim, Rua Sulaiman, Ghassan M. Taqi, Zainab J. Khashan, Khawla S. Mohammed, Hamdoon A. Khan, Riaz A. Mohammed, Salman A. A. Gold Nanoparticles and Graphene Oxide Flakes Enhance Cancer Cells’ Phagocytosis through Granzyme-Perforin-Dependent Biomechanism |
title | Gold Nanoparticles and Graphene Oxide Flakes Enhance Cancer Cells’ Phagocytosis through Granzyme-Perforin-Dependent Biomechanism |
title_full | Gold Nanoparticles and Graphene Oxide Flakes Enhance Cancer Cells’ Phagocytosis through Granzyme-Perforin-Dependent Biomechanism |
title_fullStr | Gold Nanoparticles and Graphene Oxide Flakes Enhance Cancer Cells’ Phagocytosis through Granzyme-Perforin-Dependent Biomechanism |
title_full_unstemmed | Gold Nanoparticles and Graphene Oxide Flakes Enhance Cancer Cells’ Phagocytosis through Granzyme-Perforin-Dependent Biomechanism |
title_short | Gold Nanoparticles and Graphene Oxide Flakes Enhance Cancer Cells’ Phagocytosis through Granzyme-Perforin-Dependent Biomechanism |
title_sort | gold nanoparticles and graphene oxide flakes enhance cancer cells’ phagocytosis through granzyme-perforin-dependent biomechanism |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8225074/ https://www.ncbi.nlm.nih.gov/pubmed/34073808 http://dx.doi.org/10.3390/nano11061382 |
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