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Anti-N-Methyl-D-Aspartic Acid Receptor 2 (Anti-NR2) Antibody in Neuropsychiatric Lupus Serum Damages the Blood–Brain Barrier and Enters the Brain

BACKGROUND: Brain microvessel endothelial cells constitute an important component in the blood-brain barrier. Cell-culture-based models of the blood-brain barrier (BBB) have been extensively applied in pharmacology, pathology and physiology. This study investigated effects of anti-N-methyl-D-asparti...

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Autores principales: Wang, Jing-Yuan, Zhao, Yin-Huan, Zhang, Ji-Hui, Lei, Hong-Wei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Scientific Literature, Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6346811/
https://www.ncbi.nlm.nih.gov/pubmed/30657743
http://dx.doi.org/10.12659/MSM.912389
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author Wang, Jing-Yuan
Zhao, Yin-Huan
Zhang, Ji-Hui
Lei, Hong-Wei
author_facet Wang, Jing-Yuan
Zhao, Yin-Huan
Zhang, Ji-Hui
Lei, Hong-Wei
author_sort Wang, Jing-Yuan
collection PubMed
description BACKGROUND: Brain microvessel endothelial cells constitute an important component in the blood-brain barrier. Cell-culture-based models of the blood-brain barrier (BBB) have been extensively applied in pharmacology, pathology and physiology. This study investigated effects of anti-N-methyl-D-aspartic acid receptor 2 (anti-NR2), N-methyl-D-aspartic acid (NMDA) receptor antibodies, NMDA receptor antagonists, and NMDA receptor agonists on brain microvessel endothelial cell models, and verified the effect of anti-NR2 antibody on the BBB as a receptor agonist. MATERIAL/METHODS: The primary brain microvessel endothelial cells were isolated and cultured, and an in vitro BBB model was established based on microvessel endothelial cells. Anti-NR2 antibody, glutamic acid, ifenprodil, and memantine were added in the BBB model to analyze changes in transepithelial electrical resistance (TEER) and to examine the permeability of the brain microvessel endothelial cell model. RESULTS: The results showed that TEER values were significantly decreased by the addition of anti-NR2 antibody and glutamate, but were significantly increased by the addition of ifenprodil and memantine. TEER values showed no changes when treated by anti-NR2 antibody and ifenprodil, as well as anti-NR2 antibody and memantine. When dexamethasone was added, the TEER values increased by 23.8%, 39.4%, and 29.6% by treating with anti-NR2 antibody, positive cerebrospinal fluid, and positive serum, respectively. CONCLUSIONS: Our findings show that anti-NR2 antibody in neuropsychiatric lupus serum can damage the BBB and enter the brain.
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spelling pubmed-63468112019-02-11 Anti-N-Methyl-D-Aspartic Acid Receptor 2 (Anti-NR2) Antibody in Neuropsychiatric Lupus Serum Damages the Blood–Brain Barrier and Enters the Brain Wang, Jing-Yuan Zhao, Yin-Huan Zhang, Ji-Hui Lei, Hong-Wei Med Sci Monit Lab/In Vitro Research BACKGROUND: Brain microvessel endothelial cells constitute an important component in the blood-brain barrier. Cell-culture-based models of the blood-brain barrier (BBB) have been extensively applied in pharmacology, pathology and physiology. This study investigated effects of anti-N-methyl-D-aspartic acid receptor 2 (anti-NR2), N-methyl-D-aspartic acid (NMDA) receptor antibodies, NMDA receptor antagonists, and NMDA receptor agonists on brain microvessel endothelial cell models, and verified the effect of anti-NR2 antibody on the BBB as a receptor agonist. MATERIAL/METHODS: The primary brain microvessel endothelial cells were isolated and cultured, and an in vitro BBB model was established based on microvessel endothelial cells. Anti-NR2 antibody, glutamic acid, ifenprodil, and memantine were added in the BBB model to analyze changes in transepithelial electrical resistance (TEER) and to examine the permeability of the brain microvessel endothelial cell model. RESULTS: The results showed that TEER values were significantly decreased by the addition of anti-NR2 antibody and glutamate, but were significantly increased by the addition of ifenprodil and memantine. TEER values showed no changes when treated by anti-NR2 antibody and ifenprodil, as well as anti-NR2 antibody and memantine. When dexamethasone was added, the TEER values increased by 23.8%, 39.4%, and 29.6% by treating with anti-NR2 antibody, positive cerebrospinal fluid, and positive serum, respectively. CONCLUSIONS: Our findings show that anti-NR2 antibody in neuropsychiatric lupus serum can damage the BBB and enter the brain. International Scientific Literature, Inc. 2019-01-18 /pmc/articles/PMC6346811/ /pubmed/30657743 http://dx.doi.org/10.12659/MSM.912389 Text en © Med Sci Monit, 2019 This work is licensed under Creative Common Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) )
spellingShingle Lab/In Vitro Research
Wang, Jing-Yuan
Zhao, Yin-Huan
Zhang, Ji-Hui
Lei, Hong-Wei
Anti-N-Methyl-D-Aspartic Acid Receptor 2 (Anti-NR2) Antibody in Neuropsychiatric Lupus Serum Damages the Blood–Brain Barrier and Enters the Brain
title Anti-N-Methyl-D-Aspartic Acid Receptor 2 (Anti-NR2) Antibody in Neuropsychiatric Lupus Serum Damages the Blood–Brain Barrier and Enters the Brain
title_full Anti-N-Methyl-D-Aspartic Acid Receptor 2 (Anti-NR2) Antibody in Neuropsychiatric Lupus Serum Damages the Blood–Brain Barrier and Enters the Brain
title_fullStr Anti-N-Methyl-D-Aspartic Acid Receptor 2 (Anti-NR2) Antibody in Neuropsychiatric Lupus Serum Damages the Blood–Brain Barrier and Enters the Brain
title_full_unstemmed Anti-N-Methyl-D-Aspartic Acid Receptor 2 (Anti-NR2) Antibody in Neuropsychiatric Lupus Serum Damages the Blood–Brain Barrier and Enters the Brain
title_short Anti-N-Methyl-D-Aspartic Acid Receptor 2 (Anti-NR2) Antibody in Neuropsychiatric Lupus Serum Damages the Blood–Brain Barrier and Enters the Brain
title_sort anti-n-methyl-d-aspartic acid receptor 2 (anti-nr2) antibody in neuropsychiatric lupus serum damages the blood–brain barrier and enters the brain
topic Lab/In Vitro Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6346811/
https://www.ncbi.nlm.nih.gov/pubmed/30657743
http://dx.doi.org/10.12659/MSM.912389
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