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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...

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Autores principales: Chen, Shih‐Yin, Lin, Meng‐Chieh, Tsai, Jia‐Shiuan, He, Pei‐Lin, Luo, Wen‐Ting, Herschman, Harvey, Li, Hua‐Jung
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2019
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
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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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