Progress in mimicking brain microenvironments to understand and treat neurological disorders

Neurological disorders including traumatic brain injury, stroke, primary and metastatic brain tumors, and neurodegenerative diseases affect millions of people worldwide. Disease progression is accompanied by changes in the brain microenvironment, but how these shifts in biochemical, biophysical, and...

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Main Authors: Mai T. Ngo, Brendan A. C. Harley
Format: Article
Language:English
Published: AIP Publishing LLC 2021-06-01
Series:APL Bioengineering
Online Access:http://dx.doi.org/10.1063/5.0043338
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spelling doaj-64071391055f4ca68c27892af049e6362021-07-08T13:17:23ZengAIP Publishing LLCAPL Bioengineering2473-28772021-06-0152020902020902-1910.1063/5.0043338Progress in mimicking brain microenvironments to understand and treat neurological disordersMai T. Ngo0Brendan A. C. Harley1 Department of Chemical and Biomolecular Engineering, University of Illinois at Urbana-Champaign, Urbana, Illinois 61801, USA Department of Chemical and Biomolecular Engineering, University of Illinois at Urbana-Champaign, Urbana, Illinois 61801, USANeurological disorders including traumatic brain injury, stroke, primary and metastatic brain tumors, and neurodegenerative diseases affect millions of people worldwide. Disease progression is accompanied by changes in the brain microenvironment, but how these shifts in biochemical, biophysical, and cellular properties contribute to repair outcomes or continued degeneration is largely unknown. Tissue engineering approaches can be used to develop in vitro models to understand how the brain microenvironment contributes to pathophysiological processes linked to neurological disorders and may also offer constructs that promote healing and regeneration in vivo. In this Perspective, we summarize features of the brain microenvironment in normal and pathophysiological states and highlight strategies to mimic this environment to model disease, investigate neural stem cell biology, and promote regenerative healing. We discuss current limitations and resulting opportunities to develop tissue engineering tools that more faithfully recapitulate the aspects of the brain microenvironment for both in vitro and in vivo applications.http://dx.doi.org/10.1063/5.0043338
collection DOAJ
language English
format Article
sources DOAJ
author Mai T. Ngo
Brendan A. C. Harley
spellingShingle Mai T. Ngo
Brendan A. C. Harley
Progress in mimicking brain microenvironments to understand and treat neurological disorders
APL Bioengineering
author_facet Mai T. Ngo
Brendan A. C. Harley
author_sort Mai T. Ngo
title Progress in mimicking brain microenvironments to understand and treat neurological disorders
title_short Progress in mimicking brain microenvironments to understand and treat neurological disorders
title_full Progress in mimicking brain microenvironments to understand and treat neurological disorders
title_fullStr Progress in mimicking brain microenvironments to understand and treat neurological disorders
title_full_unstemmed Progress in mimicking brain microenvironments to understand and treat neurological disorders
title_sort progress in mimicking brain microenvironments to understand and treat neurological disorders
publisher AIP Publishing LLC
series APL Bioengineering
issn 2473-2877
publishDate 2021-06-01
description Neurological disorders including traumatic brain injury, stroke, primary and metastatic brain tumors, and neurodegenerative diseases affect millions of people worldwide. Disease progression is accompanied by changes in the brain microenvironment, but how these shifts in biochemical, biophysical, and cellular properties contribute to repair outcomes or continued degeneration is largely unknown. Tissue engineering approaches can be used to develop in vitro models to understand how the brain microenvironment contributes to pathophysiological processes linked to neurological disorders and may also offer constructs that promote healing and regeneration in vivo. In this Perspective, we summarize features of the brain microenvironment in normal and pathophysiological states and highlight strategies to mimic this environment to model disease, investigate neural stem cell biology, and promote regenerative healing. We discuss current limitations and resulting opportunities to develop tissue engineering tools that more faithfully recapitulate the aspects of the brain microenvironment for both in vitro and in vivo applications.
url http://dx.doi.org/10.1063/5.0043338
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