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EP(4) Antagonist‐Elicited Extracellular Vesicles from Mesenchymal Stem Cells Rescue Cognition/Learning Deficiencies by Restoring Brain Cellular Functions
Adult brains have limited regenerative capacity. Consequently, both brain damage and neurodegenerative diseases often cause functional impairment for patients. Mesenchymal stem cells (MSCs), one type of adult stem cells, can be isolated from various adult tissues. MSCs have been used in clinical tri...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons, Inc.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6591556/ https://www.ncbi.nlm.nih.gov/pubmed/30891948 http://dx.doi.org/10.1002/sctm.18-0284 |
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author | Chen, Shih‐Yin Lin, Meng‐Chieh Tsai, Jia‐Shiuan He, Pei‐Lin Luo, Wen‐Ting Herschman, Harvey Li, Hua‐Jung |
author_facet | Chen, Shih‐Yin Lin, Meng‐Chieh Tsai, Jia‐Shiuan He, Pei‐Lin Luo, Wen‐Ting Herschman, Harvey Li, Hua‐Jung |
author_sort | Chen, Shih‐Yin |
collection | PubMed |
description | Adult brains have limited regenerative capacity. Consequently, both brain damage and neurodegenerative diseases often cause functional impairment for patients. Mesenchymal stem cells (MSCs), one type of adult stem cells, can be isolated from various adult tissues. MSCs have been used in clinical trials to treat human diseases and the therapeutic potentials of the MSC‐derived secretome and extracellular vesicles (EVs) have been under investigation. We found that blocking the prostaglandin E(2)/prostaglandin E(2) receptor 4 (PGE(2)/EP(4)) signaling pathway in MSCs with EP(4) antagonists increased EV release and promoted the sorting of specific proteins, including anti‐inflammatory cytokines and factors that modify astrocyte function, blood–brain barrier integrity, and microglial migration into the damaged hippocampus, into the EVs. Systemic administration of EP(4) antagonist‐elicited MSC EVs repaired deficiencies of cognition, learning and memory, inhibited reactive astrogliosis, attenuated extensive inflammation, reduced microglial infiltration into the damaged hippocampus, and increased blood–brain barrier integrity when administered to mice following hippocampal damage. stem cells translational medicine 2019 |
format | Online Article Text |
id | pubmed-6591556 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | John Wiley & Sons, Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-65915562019-07-09 EP(4) Antagonist‐Elicited Extracellular Vesicles from Mesenchymal Stem Cells Rescue Cognition/Learning Deficiencies by Restoring Brain Cellular Functions Chen, Shih‐Yin Lin, Meng‐Chieh Tsai, Jia‐Shiuan He, Pei‐Lin Luo, Wen‐Ting Herschman, Harvey Li, Hua‐Jung Stem Cells Transl Med Tissue Engineering and Regenerative Medicine Adult brains have limited regenerative capacity. Consequently, both brain damage and neurodegenerative diseases often cause functional impairment for patients. Mesenchymal stem cells (MSCs), one type of adult stem cells, can be isolated from various adult tissues. MSCs have been used in clinical trials to treat human diseases and the therapeutic potentials of the MSC‐derived secretome and extracellular vesicles (EVs) have been under investigation. We found that blocking the prostaglandin E(2)/prostaglandin E(2) receptor 4 (PGE(2)/EP(4)) signaling pathway in MSCs with EP(4) antagonists increased EV release and promoted the sorting of specific proteins, including anti‐inflammatory cytokines and factors that modify astrocyte function, blood–brain barrier integrity, and microglial migration into the damaged hippocampus, into the EVs. Systemic administration of EP(4) antagonist‐elicited MSC EVs repaired deficiencies of cognition, learning and memory, inhibited reactive astrogliosis, attenuated extensive inflammation, reduced microglial infiltration into the damaged hippocampus, and increased blood–brain barrier integrity when administered to mice following hippocampal damage. stem cells translational medicine 2019 John Wiley & Sons, Inc. 2019-03-19 /pmc/articles/PMC6591556/ /pubmed/30891948 http://dx.doi.org/10.1002/sctm.18-0284 Text en © 2019 The Authors. stem cells translational medicine published by Wiley Periodicals, Inc. on behalf of AlphaMed Press This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Tissue Engineering and Regenerative Medicine Chen, Shih‐Yin Lin, Meng‐Chieh Tsai, Jia‐Shiuan He, Pei‐Lin Luo, Wen‐Ting Herschman, Harvey Li, Hua‐Jung EP(4) Antagonist‐Elicited Extracellular Vesicles from Mesenchymal Stem Cells Rescue Cognition/Learning Deficiencies by Restoring Brain Cellular Functions |
title | EP(4) Antagonist‐Elicited Extracellular Vesicles from Mesenchymal Stem Cells Rescue Cognition/Learning Deficiencies by Restoring Brain Cellular Functions |
title_full | EP(4) Antagonist‐Elicited Extracellular Vesicles from Mesenchymal Stem Cells Rescue Cognition/Learning Deficiencies by Restoring Brain Cellular Functions |
title_fullStr | EP(4) Antagonist‐Elicited Extracellular Vesicles from Mesenchymal Stem Cells Rescue Cognition/Learning Deficiencies by Restoring Brain Cellular Functions |
title_full_unstemmed | EP(4) Antagonist‐Elicited Extracellular Vesicles from Mesenchymal Stem Cells Rescue Cognition/Learning Deficiencies by Restoring Brain Cellular Functions |
title_short | EP(4) Antagonist‐Elicited Extracellular Vesicles from Mesenchymal Stem Cells Rescue Cognition/Learning Deficiencies by Restoring Brain Cellular Functions |
title_sort | ep(4) antagonist‐elicited extracellular vesicles from mesenchymal stem cells rescue cognition/learning deficiencies by restoring brain cellular functions |
topic | Tissue Engineering and Regenerative Medicine |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6591556/ https://www.ncbi.nlm.nih.gov/pubmed/30891948 http://dx.doi.org/10.1002/sctm.18-0284 |
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