Cargando…
Human adipose-derived mesenchymal stem cells for acute and sub-acute TBI
In the U.S., approximately 1.7 million people suffer traumatic brain injury each year, with many enduring long-term consequences and significant medical and rehabilitation costs. The primary injury causes physical damage to neurons, glia, fiber tracts and microvasculature, which is then followed by...
Autores principales: | , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7250455/ https://www.ncbi.nlm.nih.gov/pubmed/32453741 http://dx.doi.org/10.1371/journal.pone.0233263 |
_version_ | 1783538767775137792 |
---|---|
author | Ruppert, Katherine A. Prabhakara, Karthik S. Toledano-Furman, Naama E. Udtha, Sanjna Arceneaux, Austin Q. Park, Hyeonggeun Dao, An Cox, Charles S. Olson, Scott D. |
author_facet | Ruppert, Katherine A. Prabhakara, Karthik S. Toledano-Furman, Naama E. Udtha, Sanjna Arceneaux, Austin Q. Park, Hyeonggeun Dao, An Cox, Charles S. Olson, Scott D. |
author_sort | Ruppert, Katherine A. |
collection | PubMed |
description | In the U.S., approximately 1.7 million people suffer traumatic brain injury each year, with many enduring long-term consequences and significant medical and rehabilitation costs. The primary injury causes physical damage to neurons, glia, fiber tracts and microvasculature, which is then followed by secondary injury, consisting of pathophysiological mechanisms including an immune response, inflammation, edema, excitotoxicity, oxidative damage, and cell death. Most attempts at intervention focus on protection, repair or regeneration, with regenerative medicine becoming an intensively studied area over the past decade. The use of stem cells has been studied in many disease and injury models, using stem cells from a variety of sources and applications. In this study, human adipose-derived mesenchymal stromal cells (MSCs) were administered at early (3 days) and delayed (14 days) time points after controlled cortical impact (CCI) injury in rats. Animals were routinely assessed for neurological and vestibulomotor deficits, and at 32 days post-injury, brain tissue was processed by flow cytometry and immunohistochemistry to analyze neuroinflammation. Treatment with HB-adMSC at either 3d or 14d after injury resulted in significant improvements in neurocognitive outcome and a change in neuroinflammation one month after injury. |
format | Online Article Text |
id | pubmed-7250455 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-72504552020-06-08 Human adipose-derived mesenchymal stem cells for acute and sub-acute TBI Ruppert, Katherine A. Prabhakara, Karthik S. Toledano-Furman, Naama E. Udtha, Sanjna Arceneaux, Austin Q. Park, Hyeonggeun Dao, An Cox, Charles S. Olson, Scott D. PLoS One Research Article In the U.S., approximately 1.7 million people suffer traumatic brain injury each year, with many enduring long-term consequences and significant medical and rehabilitation costs. The primary injury causes physical damage to neurons, glia, fiber tracts and microvasculature, which is then followed by secondary injury, consisting of pathophysiological mechanisms including an immune response, inflammation, edema, excitotoxicity, oxidative damage, and cell death. Most attempts at intervention focus on protection, repair or regeneration, with regenerative medicine becoming an intensively studied area over the past decade. The use of stem cells has been studied in many disease and injury models, using stem cells from a variety of sources and applications. In this study, human adipose-derived mesenchymal stromal cells (MSCs) were administered at early (3 days) and delayed (14 days) time points after controlled cortical impact (CCI) injury in rats. Animals were routinely assessed for neurological and vestibulomotor deficits, and at 32 days post-injury, brain tissue was processed by flow cytometry and immunohistochemistry to analyze neuroinflammation. Treatment with HB-adMSC at either 3d or 14d after injury resulted in significant improvements in neurocognitive outcome and a change in neuroinflammation one month after injury. Public Library of Science 2020-05-26 /pmc/articles/PMC7250455/ /pubmed/32453741 http://dx.doi.org/10.1371/journal.pone.0233263 Text en © 2020 Ruppert et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Ruppert, Katherine A. Prabhakara, Karthik S. Toledano-Furman, Naama E. Udtha, Sanjna Arceneaux, Austin Q. Park, Hyeonggeun Dao, An Cox, Charles S. Olson, Scott D. Human adipose-derived mesenchymal stem cells for acute and sub-acute TBI |
title | Human adipose-derived mesenchymal stem cells for acute and sub-acute TBI |
title_full | Human adipose-derived mesenchymal stem cells for acute and sub-acute TBI |
title_fullStr | Human adipose-derived mesenchymal stem cells for acute and sub-acute TBI |
title_full_unstemmed | Human adipose-derived mesenchymal stem cells for acute and sub-acute TBI |
title_short | Human adipose-derived mesenchymal stem cells for acute and sub-acute TBI |
title_sort | human adipose-derived mesenchymal stem cells for acute and sub-acute tbi |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7250455/ https://www.ncbi.nlm.nih.gov/pubmed/32453741 http://dx.doi.org/10.1371/journal.pone.0233263 |
work_keys_str_mv | AT ruppertkatherinea humanadiposederivedmesenchymalstemcellsforacuteandsubacutetbi AT prabhakarakarthiks humanadiposederivedmesenchymalstemcellsforacuteandsubacutetbi AT toledanofurmannaamae humanadiposederivedmesenchymalstemcellsforacuteandsubacutetbi AT udthasanjna humanadiposederivedmesenchymalstemcellsforacuteandsubacutetbi AT arceneauxaustinq humanadiposederivedmesenchymalstemcellsforacuteandsubacutetbi AT parkhyeonggeun humanadiposederivedmesenchymalstemcellsforacuteandsubacutetbi AT daoan humanadiposederivedmesenchymalstemcellsforacuteandsubacutetbi AT coxcharless humanadiposederivedmesenchymalstemcellsforacuteandsubacutetbi AT olsonscottd humanadiposederivedmesenchymalstemcellsforacuteandsubacutetbi |