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Quantum Dot Biomimetic for SARS-CoV-2 to Interrogate Blood–Brain Barrier Damage Relevant to NeuroCOVID Brain Inflammation

[Image: see text] Despite limited evidence for infection of SARS-CoV-2 in the central nervous system, cognitive impairment is a common complication reported in “recovered” COVID-19 patients. Identification of the origins of these neurological impairments is essential to inform therapeutic designs ag...

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Autores principales: Chiang, Wesley, Stout, Angela, Yanchik-Slade, Francine, Li, Herman, Terrando, Niccolò, Nilsson, Bradley L., Gelbard, Harris A., Krauss, Todd D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2023
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10463222/
https://www.ncbi.nlm.nih.gov/pubmed/37649833
http://dx.doi.org/10.1021/acsanm.3c02719
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author Chiang, Wesley
Stout, Angela
Yanchik-Slade, Francine
Li, Herman
Terrando, Niccolò
Nilsson, Bradley L.
Gelbard, Harris A.
Krauss, Todd D.
author_facet Chiang, Wesley
Stout, Angela
Yanchik-Slade, Francine
Li, Herman
Terrando, Niccolò
Nilsson, Bradley L.
Gelbard, Harris A.
Krauss, Todd D.
author_sort Chiang, Wesley
collection PubMed
description [Image: see text] Despite limited evidence for infection of SARS-CoV-2 in the central nervous system, cognitive impairment is a common complication reported in “recovered” COVID-19 patients. Identification of the origins of these neurological impairments is essential to inform therapeutic designs against them. However, such studies are limited, in part, by the current status of high-fidelity probes to visually investigate the effects of SARS-CoV-2 on the system of blood vessels and nerve cells in the brain, called the neurovascular unit. Here, we report that nanocrystal quantum dot micelles decorated with spike protein (COVID-QDs) are able to interrogate neurological damage due to SARS-CoV-2. In a transwell co-culture model of the neurovascular unit, exposure of brain endothelial cells to COVID-QDs elicited an inflammatory response in neurons and astrocytes without direct interaction with the COVID-QDs. These results provide compelling evidence of an inflammatory response without direct exposure to SARS-CoV-2-like nanoparticles. Additionally, we found that pretreatment with a neuro-protective molecule prevented endothelial cell damage resulting in substantial neurological protection. These results will accelerate studies into the mechanisms by which SARS-CoV-2 mediates neurologic dysfunction.
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spelling pubmed-104632222023-08-30 Quantum Dot Biomimetic for SARS-CoV-2 to Interrogate Blood–Brain Barrier Damage Relevant to NeuroCOVID Brain Inflammation Chiang, Wesley Stout, Angela Yanchik-Slade, Francine Li, Herman Terrando, Niccolò Nilsson, Bradley L. Gelbard, Harris A. Krauss, Todd D. ACS Appl Nano Mater [Image: see text] Despite limited evidence for infection of SARS-CoV-2 in the central nervous system, cognitive impairment is a common complication reported in “recovered” COVID-19 patients. Identification of the origins of these neurological impairments is essential to inform therapeutic designs against them. However, such studies are limited, in part, by the current status of high-fidelity probes to visually investigate the effects of SARS-CoV-2 on the system of blood vessels and nerve cells in the brain, called the neurovascular unit. Here, we report that nanocrystal quantum dot micelles decorated with spike protein (COVID-QDs) are able to interrogate neurological damage due to SARS-CoV-2. In a transwell co-culture model of the neurovascular unit, exposure of brain endothelial cells to COVID-QDs elicited an inflammatory response in neurons and astrocytes without direct interaction with the COVID-QDs. These results provide compelling evidence of an inflammatory response without direct exposure to SARS-CoV-2-like nanoparticles. Additionally, we found that pretreatment with a neuro-protective molecule prevented endothelial cell damage resulting in substantial neurological protection. These results will accelerate studies into the mechanisms by which SARS-CoV-2 mediates neurologic dysfunction. American Chemical Society 2023-08-07 /pmc/articles/PMC10463222/ /pubmed/37649833 http://dx.doi.org/10.1021/acsanm.3c02719 Text en © 2023 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Chiang, Wesley
Stout, Angela
Yanchik-Slade, Francine
Li, Herman
Terrando, Niccolò
Nilsson, Bradley L.
Gelbard, Harris A.
Krauss, Todd D.
Quantum Dot Biomimetic for SARS-CoV-2 to Interrogate Blood–Brain Barrier Damage Relevant to NeuroCOVID Brain Inflammation
title Quantum Dot Biomimetic for SARS-CoV-2 to Interrogate Blood–Brain Barrier Damage Relevant to NeuroCOVID Brain Inflammation
title_full Quantum Dot Biomimetic for SARS-CoV-2 to Interrogate Blood–Brain Barrier Damage Relevant to NeuroCOVID Brain Inflammation
title_fullStr Quantum Dot Biomimetic for SARS-CoV-2 to Interrogate Blood–Brain Barrier Damage Relevant to NeuroCOVID Brain Inflammation
title_full_unstemmed Quantum Dot Biomimetic for SARS-CoV-2 to Interrogate Blood–Brain Barrier Damage Relevant to NeuroCOVID Brain Inflammation
title_short Quantum Dot Biomimetic for SARS-CoV-2 to Interrogate Blood–Brain Barrier Damage Relevant to NeuroCOVID Brain Inflammation
title_sort quantum dot biomimetic for sars-cov-2 to interrogate blood–brain barrier damage relevant to neurocovid brain inflammation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10463222/
https://www.ncbi.nlm.nih.gov/pubmed/37649833
http://dx.doi.org/10.1021/acsanm.3c02719
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