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Immunohistochemistry of IL-1β, IL-6 and TNF-α in spleens of mice treated with gold nanoparticles

Gold nanoparticles (AuNPs) possess considerable biocompatibility and therefore gaining more attention for their biomedical applications. Previous studies have shown the transient increase in pro-inflammatory cytokines expression in different organs of rats and mice exposed to AuNPs. Structural chang...

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Autores principales: Khan, Haseeb A., Ibrahim, Khalid E., Alrashood, Sara T., Alamery, Salman, Alrokayan, Salman H., Al-Harbi, Najla, Al-Mutary, Mohsen G., Sobki, Samia H., Khan, Isra
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7105655/
https://www.ncbi.nlm.nih.gov/pubmed/32256179
http://dx.doi.org/10.1016/j.sjbs.2020.01.025
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author Khan, Haseeb A.
Ibrahim, Khalid E.
Alrashood, Sara T.
Alamery, Salman
Alrokayan, Salman H.
Al-Harbi, Najla
Al-Mutary, Mohsen G.
Sobki, Samia H.
Khan, Isra
author_facet Khan, Haseeb A.
Ibrahim, Khalid E.
Alrashood, Sara T.
Alamery, Salman
Alrokayan, Salman H.
Al-Harbi, Najla
Al-Mutary, Mohsen G.
Sobki, Samia H.
Khan, Isra
author_sort Khan, Haseeb A.
collection PubMed
description Gold nanoparticles (AuNPs) possess considerable biocompatibility and therefore gaining more attention for their biomedical applications. Previous studies have shown the transient increase in pro-inflammatory cytokines expression in different organs of rats and mice exposed to AuNPs. Structural changes in the spleen of mice treated with AuNPs have also been reported. This investigation was aimed to study the immunostaining of IL-1β, IL-6 and TNF-α in mice treated with different sizes of AuNPs. The animals were divided into 7 groups of 4 animals in each group. One group received saline and served as control. Two sets of three groups were treated with 5 nm, 20 nm and 50 nm diameter AuNPs. One set was sacrificed on day 1 and the other on day 7 following the AuNPs injections. Spleens were dissected out and promptly fixed in formalin for 3 days and then processed for IL-1β, IL-6 and TNF-α immunostaining using target-specific antibodies. The immunoreactivities of IL-1β and IL-6 were increased with the increase of AuNP size. The immunostaining of IL-1β in spleen of 20 nm AuNP treated mice was subsequently decreased on day 7 whereas it persisted in 50 nm AuNP group. The increase in the immunoreactivity of IL-6 on day 1 was decreased on day 7 in the spleens of mice treated with 20 nm or 50 nm AuNPs. The immunostaining of TNF-α was found to be negative in all the treatment groups. In conclusion, the size of AuNPs plays an important role in the expression of proinflammatory cytokines in mouse spleen; small size (5 nm) AuNPs caused minimal effect, whereas larger (50 nm) AuNPs produced intense immunostaining.
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spelling pubmed-71056552020-03-31 Immunohistochemistry of IL-1β, IL-6 and TNF-α in spleens of mice treated with gold nanoparticles Khan, Haseeb A. Ibrahim, Khalid E. Alrashood, Sara T. Alamery, Salman Alrokayan, Salman H. Al-Harbi, Najla Al-Mutary, Mohsen G. Sobki, Samia H. Khan, Isra Saudi J Biol Sci Article Gold nanoparticles (AuNPs) possess considerable biocompatibility and therefore gaining more attention for their biomedical applications. Previous studies have shown the transient increase in pro-inflammatory cytokines expression in different organs of rats and mice exposed to AuNPs. Structural changes in the spleen of mice treated with AuNPs have also been reported. This investigation was aimed to study the immunostaining of IL-1β, IL-6 and TNF-α in mice treated with different sizes of AuNPs. The animals were divided into 7 groups of 4 animals in each group. One group received saline and served as control. Two sets of three groups were treated with 5 nm, 20 nm and 50 nm diameter AuNPs. One set was sacrificed on day 1 and the other on day 7 following the AuNPs injections. Spleens were dissected out and promptly fixed in formalin for 3 days and then processed for IL-1β, IL-6 and TNF-α immunostaining using target-specific antibodies. The immunoreactivities of IL-1β and IL-6 were increased with the increase of AuNP size. The immunostaining of IL-1β in spleen of 20 nm AuNP treated mice was subsequently decreased on day 7 whereas it persisted in 50 nm AuNP group. The increase in the immunoreactivity of IL-6 on day 1 was decreased on day 7 in the spleens of mice treated with 20 nm or 50 nm AuNPs. The immunostaining of TNF-α was found to be negative in all the treatment groups. In conclusion, the size of AuNPs plays an important role in the expression of proinflammatory cytokines in mouse spleen; small size (5 nm) AuNPs caused minimal effect, whereas larger (50 nm) AuNPs produced intense immunostaining. Elsevier 2020-04 2020-01-30 /pmc/articles/PMC7105655/ /pubmed/32256179 http://dx.doi.org/10.1016/j.sjbs.2020.01.025 Text en © 2020 Published by Elsevier B.V. on behalf of King Saud University. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Khan, Haseeb A.
Ibrahim, Khalid E.
Alrashood, Sara T.
Alamery, Salman
Alrokayan, Salman H.
Al-Harbi, Najla
Al-Mutary, Mohsen G.
Sobki, Samia H.
Khan, Isra
Immunohistochemistry of IL-1β, IL-6 and TNF-α in spleens of mice treated with gold nanoparticles
title Immunohistochemistry of IL-1β, IL-6 and TNF-α in spleens of mice treated with gold nanoparticles
title_full Immunohistochemistry of IL-1β, IL-6 and TNF-α in spleens of mice treated with gold nanoparticles
title_fullStr Immunohistochemistry of IL-1β, IL-6 and TNF-α in spleens of mice treated with gold nanoparticles
title_full_unstemmed Immunohistochemistry of IL-1β, IL-6 and TNF-α in spleens of mice treated with gold nanoparticles
title_short Immunohistochemistry of IL-1β, IL-6 and TNF-α in spleens of mice treated with gold nanoparticles
title_sort immunohistochemistry of il-1β, il-6 and tnf-α in spleens of mice treated with gold nanoparticles
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7105655/
https://www.ncbi.nlm.nih.gov/pubmed/32256179
http://dx.doi.org/10.1016/j.sjbs.2020.01.025
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