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Microfluidic and Microscale Assays to Examine Regenerative Strategies in the Neuro Retina
Bioengineering systems have transformed scientific knowledge of cellular behaviors in the nervous system (NS) and pioneered innovative, regenerative therapies to treat adult neural disorders. Microscale systems with characteristic lengths of single to hundreds of microns have examined the developmen...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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MDPI
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7763644/ https://www.ncbi.nlm.nih.gov/pubmed/33316971 http://dx.doi.org/10.3390/mi11121089 |
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author | Vazquez, Maribel |
author_facet | Vazquez, Maribel |
author_sort | Vazquez, Maribel |
collection | PubMed |
description | Bioengineering systems have transformed scientific knowledge of cellular behaviors in the nervous system (NS) and pioneered innovative, regenerative therapies to treat adult neural disorders. Microscale systems with characteristic lengths of single to hundreds of microns have examined the development and specialized behaviors of numerous neuromuscular and neurosensory components of the NS. The visual system is comprised of the eye sensory organ and its connecting pathways to the visual cortex. Significant vision loss arises from dysfunction in the retina, the photosensitive tissue at the eye posterior that achieves phototransduction of light to form images in the brain. Retinal regenerative medicine has embraced microfluidic technologies to manipulate stem-like cells for transplantation therapies, where de/differentiated cells are introduced within adult tissue to replace dysfunctional or damaged neurons. Microfluidic systems coupled with stem cell biology and biomaterials have produced exciting advances to restore vision. The current article reviews contemporary microfluidic technologies and microfluidics-enhanced bioassays, developed to interrogate cellular responses to adult retinal cues. The focus is on applications of microfluidics and microscale assays within mammalian sensory retina, or neuro retina, comprised of five types of retinal neurons (photoreceptors, horizontal, bipolar, amacrine, retinal ganglion) and one neuroglia (Müller), but excludes the non-sensory, retinal pigmented epithelium. |
format | Online Article Text |
id | pubmed-7763644 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-77636442020-12-27 Microfluidic and Microscale Assays to Examine Regenerative Strategies in the Neuro Retina Vazquez, Maribel Micromachines (Basel) Review Bioengineering systems have transformed scientific knowledge of cellular behaviors in the nervous system (NS) and pioneered innovative, regenerative therapies to treat adult neural disorders. Microscale systems with characteristic lengths of single to hundreds of microns have examined the development and specialized behaviors of numerous neuromuscular and neurosensory components of the NS. The visual system is comprised of the eye sensory organ and its connecting pathways to the visual cortex. Significant vision loss arises from dysfunction in the retina, the photosensitive tissue at the eye posterior that achieves phototransduction of light to form images in the brain. Retinal regenerative medicine has embraced microfluidic technologies to manipulate stem-like cells for transplantation therapies, where de/differentiated cells are introduced within adult tissue to replace dysfunctional or damaged neurons. Microfluidic systems coupled with stem cell biology and biomaterials have produced exciting advances to restore vision. The current article reviews contemporary microfluidic technologies and microfluidics-enhanced bioassays, developed to interrogate cellular responses to adult retinal cues. The focus is on applications of microfluidics and microscale assays within mammalian sensory retina, or neuro retina, comprised of five types of retinal neurons (photoreceptors, horizontal, bipolar, amacrine, retinal ganglion) and one neuroglia (Müller), but excludes the non-sensory, retinal pigmented epithelium. MDPI 2020-12-09 /pmc/articles/PMC7763644/ /pubmed/33316971 http://dx.doi.org/10.3390/mi11121089 Text en © 2020 by the author. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Vazquez, Maribel Microfluidic and Microscale Assays to Examine Regenerative Strategies in the Neuro Retina |
title | Microfluidic and Microscale Assays to Examine Regenerative Strategies in the Neuro Retina |
title_full | Microfluidic and Microscale Assays to Examine Regenerative Strategies in the Neuro Retina |
title_fullStr | Microfluidic and Microscale Assays to Examine Regenerative Strategies in the Neuro Retina |
title_full_unstemmed | Microfluidic and Microscale Assays to Examine Regenerative Strategies in the Neuro Retina |
title_short | Microfluidic and Microscale Assays to Examine Regenerative Strategies in the Neuro Retina |
title_sort | microfluidic and microscale assays to examine regenerative strategies in the neuro retina |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7763644/ https://www.ncbi.nlm.nih.gov/pubmed/33316971 http://dx.doi.org/10.3390/mi11121089 |
work_keys_str_mv | AT vazquezmaribel microfluidicandmicroscaleassaystoexamineregenerativestrategiesintheneuroretina |