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Stem cell secretome derived from human amniotic fluid affords neuroprotection in an ischemic model

Human amniotic fluid stem cells (hAFSCs) are growing in interest; yet, little is understood about their secretome and neuroprotective actions in different diseases, including stroke. When stem cells are grown in vitro, they release an array of cytokines and growth factors that can stimulate neuropro...

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Detalles Bibliográficos
Autores principales: Kingsbury, Chase, Stuppia, Liborio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8057106/
https://www.ncbi.nlm.nih.gov/pubmed/34084972
http://dx.doi.org/10.4103/bc.bc_8_21
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author Kingsbury, Chase
Stuppia, Liborio
author_facet Kingsbury, Chase
Stuppia, Liborio
author_sort Kingsbury, Chase
collection PubMed
description Human amniotic fluid stem cells (hAFSCs) are growing in interest; yet, little is understood about their secretome and neuroprotective actions in different diseases, including stroke. When stem cells are grown in vitro, they release an array of cytokines and growth factors that can stimulate neuroprotective processes. Furthermore, administering secretome rather than cells may be a safer route for patients who are at risk for rejection, promoting innate restorative processes. Current literature implicates that the miRNA contents of such secretome, more specifically exosomes, may regulate the effectiveness of secretome administration. In this review, we explore what factors may promote pro-survival and pro-apoptotic pathways after the administration of hAFSCs-derived secretome in ischemic models.
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spelling pubmed-80571062021-06-02 Stem cell secretome derived from human amniotic fluid affords neuroprotection in an ischemic model Kingsbury, Chase Stuppia, Liborio Brain Circ Review Article Human amniotic fluid stem cells (hAFSCs) are growing in interest; yet, little is understood about their secretome and neuroprotective actions in different diseases, including stroke. When stem cells are grown in vitro, they release an array of cytokines and growth factors that can stimulate neuroprotective processes. Furthermore, administering secretome rather than cells may be a safer route for patients who are at risk for rejection, promoting innate restorative processes. Current literature implicates that the miRNA contents of such secretome, more specifically exosomes, may regulate the effectiveness of secretome administration. In this review, we explore what factors may promote pro-survival and pro-apoptotic pathways after the administration of hAFSCs-derived secretome in ischemic models. Wolters Kluwer - Medknow 2021-03-30 /pmc/articles/PMC8057106/ /pubmed/34084972 http://dx.doi.org/10.4103/bc.bc_8_21 Text en Copyright: © 2021 Brain Circulation https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Review Article
Kingsbury, Chase
Stuppia, Liborio
Stem cell secretome derived from human amniotic fluid affords neuroprotection in an ischemic model
title Stem cell secretome derived from human amniotic fluid affords neuroprotection in an ischemic model
title_full Stem cell secretome derived from human amniotic fluid affords neuroprotection in an ischemic model
title_fullStr Stem cell secretome derived from human amniotic fluid affords neuroprotection in an ischemic model
title_full_unstemmed Stem cell secretome derived from human amniotic fluid affords neuroprotection in an ischemic model
title_short Stem cell secretome derived from human amniotic fluid affords neuroprotection in an ischemic model
title_sort stem cell secretome derived from human amniotic fluid affords neuroprotection in an ischemic model
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8057106/
https://www.ncbi.nlm.nih.gov/pubmed/34084972
http://dx.doi.org/10.4103/bc.bc_8_21
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