Evidence map›Paper›PMID 37649833›Full record

ArticleACS applied nano materials2023

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

Wesley Chiang, Angela Stout, Francine Yanchik-Slade, Herman Li, Niccolò Terrando, Bradley L Nilsson, Harris A Gelbard, Todd D Krauss

Open access · hybridAbstract read
In one paragraph

Article in ACS applied nano materials, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
2.3field-weighted citation impact, top 11% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

7 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Review
  6. Article
  7. Infectious Diseases.Advances in neurobiology · 2024
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 3 institutions in 1 country.

Wesley ChiangDepartment of Biochemistry and Biophysics, Center for Neurotherapeutics Discovery and Department of Neurology, and Departments of Pediatrics, Neuroscience, and Microbiology and Immunology, University of Rochester Medical Center, Rochester, New York 14642, United States.ORCID https://orcid.org/0000-0003-0847-2056
Angela StoutDepartment of Biochemistry and Biophysics, Center for Neurotherapeutics Discovery and Department of Neurology, and Departments of Pediatrics, Neuroscience, and Microbiology and Immunology, University of Rochester Medical Center, Rochester, New York 14642, United States.
Francine Yanchik-SladeDepartment of Chemistry and The Institute of Optics, University of Rochester, Rochester, New York 14627, United States.ORCID https://orcid.org/0000-0002-3816-9990
Herman LiDepartment of Biochemistry and Biophysics, Center for Neurotherapeutics Discovery and Department of Neurology, and Departments of Pediatrics, Neuroscience, and Microbiology and Immunology, University of Rochester Medical Center, Rochester, New York 14642, United States.ORCID https://orcid.org/0000-0003-2471-8562
Niccolò TerrandoDepartment of Anesthesiology, Duke University Medical Center, Durham, North Carolina 27710, United States.ORCID https://orcid.org/0000-0003-1803-5853
Bradley L NilssonDepartment of Chemistry and The Institute of Optics, University of Rochester, Rochester, New York 14627, United States.ORCID https://orcid.org/0000-0003-1193-3693
Harris A GelbardDepartment of Biochemistry and Biophysics, Center for Neurotherapeutics Discovery and Department of Neurology, and Departments of Pediatrics, Neuroscience, and Microbiology and Immunology, University of Rochester Medical Center, Rochester, New York 14642, United States.
Todd D KraussDepartment of Chemistry and The Institute of Optics, University of Rochester, Rochester, New York 14627, United States.ORCID https://orcid.org/0000-0002-4860-874X
University of Rochester Medical Center · USUniversity of Rochester · USDuke Medical Center · US

Funding

Neurovascular dysfunction in delirium superimposed on dementiaR01AG057525 · NIA · DUKE UNIVERSITY · PI Niccolo Terrando · 2017 to 2026
$6.7M
Immunovascular interactions in postoperative delirium superimposed on dementia (DSD).RF1AG079138 · NIA · DUKE UNIVERSITY · PI GELBARD, HARRIS A, TERRANDO, NICCOLO · 2022 to 2025
$3.6M
Training in Wellness and Resiliency at the University of Rochester Medical Center and College of Arts, Sciences & EngineeringT32GM135134 · NIGMS · UNIVERSITY OF ROCHESTER · PI Jeffrey J Hayes, Lynne E Maquat · 2020 to 2026
$2.9M
NIH Training Grant in the Chemistry-Biology InterfaceT32GM118283 · NIGMS · UNIVERSITY OF ROCHESTER · PI BREN, KARA L., FASAN, RUDI · 2017 to 2021
$850k
Immunoprofiling postoperative delirium during aging and neurodegenerationR21AG074232 · NIA · UNIVERSITY OF ROCHESTER · PI GELBARD, HARRIS A, TERRANDO, NICCOLO · 2021 to 2022
$438k
Nanocrystal Quantum Dot Biomimetics of SARS-CoV-2 to Interrogate Neutrophil-Mediated Neuroinflammation at the Blood-Brain BarrierR21NS128502 · NINDS · UNIVERSITY OF ROCHESTER · PI GELBARD, HARRIS A, KRAUSS, TODD D · 2022 to 2022
$424k
Matrix-Assisted Laser Desorption Ionization Time-of-Flight (MALDI-TOF/TOF) Mass SpectrometerS10OD030302 · OD · UNIVERSITY OF ROCHESTER · PI NILSSON, BRADLEY L. · 2021 to 2021
$304k
NIA NIH HHS R01 AG057525NIA NIH HHS R21 AG074232NIA NIH HHS RF1 AG079138NIGMS NIH HHS T32 GM118283NIGMS NIH HHS T32 GM135134NIH HHS S10 OD030302NINDS NIH HHS R21 NS128502
6 · The paper itself

Abstract

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.

Identifiers

PMID37649833
PMCPMC10463222
OpenAlexW4385622340

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.