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Erythrocytes, a New Contributor to Age‐Associated Loss of Blood–Brain Barrier Integrity

Blood exchanges between young and old partners demonstrate old blood has a detrimental effect on brain health of young animals. Previous studies primarily investigate soluble blood factors, such as transforming growth factor‐beta, on the brain and the blood–brain barrier (BBB). However, the role of...

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Autores principales: Amiri, Payam, DeCastro, Jonalyn, Littig, Joshua, Lu, Hsiang‐Wei, Liu, Chao, Conboy, Irina, Aran, Kiana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8529433/
https://www.ncbi.nlm.nih.gov/pubmed/34396716
http://dx.doi.org/10.1002/advs.202101912
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author Amiri, Payam
DeCastro, Jonalyn
Littig, Joshua
Lu, Hsiang‐Wei
Liu, Chao
Conboy, Irina
Aran, Kiana
author_facet Amiri, Payam
DeCastro, Jonalyn
Littig, Joshua
Lu, Hsiang‐Wei
Liu, Chao
Conboy, Irina
Aran, Kiana
author_sort Amiri, Payam
collection PubMed
description Blood exchanges between young and old partners demonstrate old blood has a detrimental effect on brain health of young animals. Previous studies primarily investigate soluble blood factors, such as transforming growth factor‐beta, on the brain and the blood–brain barrier (BBB). However, the role of blood cellular components, particularly erythrocytes, has not been defined. Erythrocyte morphology and rigidity change as mammals age, altering their transport within the capillary bed. This impacts downstream biological events, such as the release of reactive oxygen species and hemoglobin, potentially compromising the BBB. Here, a micro electrical BBB (µE‐BBB), with cocultured endothelial and astrocytic cells, and a built‐in trans‐endothelial electrical resistance (TEER) system is described to monitor the effect of capillary shear stress on erythrocytes derived from young and old mice and people and the subsequent effects of these cells on BBB integrity. This is monitored by the passage of fluorescein isothiocyanate‐dextran and real‐time profiling of TEER across the BBB after old and young erythrocyte exposure. Compared to young erythrocytes, old erythrocytes induce an increased permeability by 42% and diminished TEER by 2.9% of the µE‐BBB. These results suggest that changes in circulating erythrocytes are a biomarker of aging in the context of BBB integrity.
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spelling pubmed-85294332021-10-27 Erythrocytes, a New Contributor to Age‐Associated Loss of Blood–Brain Barrier Integrity Amiri, Payam DeCastro, Jonalyn Littig, Joshua Lu, Hsiang‐Wei Liu, Chao Conboy, Irina Aran, Kiana Adv Sci (Weinh) Research Articles Blood exchanges between young and old partners demonstrate old blood has a detrimental effect on brain health of young animals. Previous studies primarily investigate soluble blood factors, such as transforming growth factor‐beta, on the brain and the blood–brain barrier (BBB). However, the role of blood cellular components, particularly erythrocytes, has not been defined. Erythrocyte morphology and rigidity change as mammals age, altering their transport within the capillary bed. This impacts downstream biological events, such as the release of reactive oxygen species and hemoglobin, potentially compromising the BBB. Here, a micro electrical BBB (µE‐BBB), with cocultured endothelial and astrocytic cells, and a built‐in trans‐endothelial electrical resistance (TEER) system is described to monitor the effect of capillary shear stress on erythrocytes derived from young and old mice and people and the subsequent effects of these cells on BBB integrity. This is monitored by the passage of fluorescein isothiocyanate‐dextran and real‐time profiling of TEER across the BBB after old and young erythrocyte exposure. Compared to young erythrocytes, old erythrocytes induce an increased permeability by 42% and diminished TEER by 2.9% of the µE‐BBB. These results suggest that changes in circulating erythrocytes are a biomarker of aging in the context of BBB integrity. John Wiley and Sons Inc. 2021-08-16 /pmc/articles/PMC8529433/ /pubmed/34396716 http://dx.doi.org/10.1002/advs.202101912 Text en © 2021 The Authors. Advanced Science published by Wiley‐VCH GmbH https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Amiri, Payam
DeCastro, Jonalyn
Littig, Joshua
Lu, Hsiang‐Wei
Liu, Chao
Conboy, Irina
Aran, Kiana
Erythrocytes, a New Contributor to Age‐Associated Loss of Blood–Brain Barrier Integrity
title Erythrocytes, a New Contributor to Age‐Associated Loss of Blood–Brain Barrier Integrity
title_full Erythrocytes, a New Contributor to Age‐Associated Loss of Blood–Brain Barrier Integrity
title_fullStr Erythrocytes, a New Contributor to Age‐Associated Loss of Blood–Brain Barrier Integrity
title_full_unstemmed Erythrocytes, a New Contributor to Age‐Associated Loss of Blood–Brain Barrier Integrity
title_short Erythrocytes, a New Contributor to Age‐Associated Loss of Blood–Brain Barrier Integrity
title_sort erythrocytes, a new contributor to age‐associated loss of blood–brain barrier integrity
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8529433/
https://www.ncbi.nlm.nih.gov/pubmed/34396716
http://dx.doi.org/10.1002/advs.202101912
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