The Immunomodulatory Capacity of Induced Pluripotent Stem Cells in the Post-stroke Environment

Inflammation has proven to be a key contributing factor to the pathogenesis of ischemic and hemorrhagic stroke. This sequential and progressive response, marked by proliferation of resident immune cells and recruitment of peripheral immune populations, results in increased oxidative stress, and neur...

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Main Authors: Samantha E. Spellicy, David C. Hess
Format: Article
Language:English
Published: Frontiers Media S.A. 2021-03-01
Series:Frontiers in Cell and Developmental Biology
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fcell.2021.647415/full
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spelling doaj-b0474f77f9224b908a8cb6c5d03059422021-03-16T05:19:03ZengFrontiers Media S.A.Frontiers in Cell and Developmental Biology2296-634X2021-03-01910.3389/fcell.2021.647415647415The Immunomodulatory Capacity of Induced Pluripotent Stem Cells in the Post-stroke EnvironmentSamantha E. Spellicy0David C. Hess1MD-Ph.D. Program, Medical College of Georgia at Augusta University, Augusta, GA, United StatesDean’s Office, Medical College of Georgia at Augusta University, Augusta, GA, United StatesInflammation has proven to be a key contributing factor to the pathogenesis of ischemic and hemorrhagic stroke. This sequential and progressive response, marked by proliferation of resident immune cells and recruitment of peripheral immune populations, results in increased oxidative stress, and neuronal cell death. Therapeutics aimed at quelling various stages of this post-stroke inflammatory response have shown promise recently, one of which being differentiated induced pluripotent stem cells (iPSCs). While direct repopulation of damaged tissues and enhanced neurogenesis are hypothesized to encompass some of the therapeutic potential of iPSCs, recent evidence has demonstrated a substantial paracrine effect on neuroinflammation. Specifically, investigation of iPSCs, iPSC-neural progenitor cells (iPSC-NPCs), and iPSC-neuroepithelial like stem cells (iPSC-lt-NESC) has demonstrated significant immunomodulation of proinflammatory signaling and endogenous inflammatory cell populations, such as microglia. This review aims to examine the mechanisms by which iPSCs mediate neuroinflammation in the post-stroke environment, as well as delineate avenues for further investigation.https://www.frontiersin.org/articles/10.3389/fcell.2021.647415/fullinduced pluripotent stem cellsstrokeiNSCsneuroinflammationstem cells
collection DOAJ
language English
format Article
sources DOAJ
author Samantha E. Spellicy
David C. Hess
spellingShingle Samantha E. Spellicy
David C. Hess
The Immunomodulatory Capacity of Induced Pluripotent Stem Cells in the Post-stroke Environment
Frontiers in Cell and Developmental Biology
induced pluripotent stem cells
stroke
iNSCs
neuroinflammation
stem cells
author_facet Samantha E. Spellicy
David C. Hess
author_sort Samantha E. Spellicy
title The Immunomodulatory Capacity of Induced Pluripotent Stem Cells in the Post-stroke Environment
title_short The Immunomodulatory Capacity of Induced Pluripotent Stem Cells in the Post-stroke Environment
title_full The Immunomodulatory Capacity of Induced Pluripotent Stem Cells in the Post-stroke Environment
title_fullStr The Immunomodulatory Capacity of Induced Pluripotent Stem Cells in the Post-stroke Environment
title_full_unstemmed The Immunomodulatory Capacity of Induced Pluripotent Stem Cells in the Post-stroke Environment
title_sort immunomodulatory capacity of induced pluripotent stem cells in the post-stroke environment
publisher Frontiers Media S.A.
series Frontiers in Cell and Developmental Biology
issn 2296-634X
publishDate 2021-03-01
description Inflammation has proven to be a key contributing factor to the pathogenesis of ischemic and hemorrhagic stroke. This sequential and progressive response, marked by proliferation of resident immune cells and recruitment of peripheral immune populations, results in increased oxidative stress, and neuronal cell death. Therapeutics aimed at quelling various stages of this post-stroke inflammatory response have shown promise recently, one of which being differentiated induced pluripotent stem cells (iPSCs). While direct repopulation of damaged tissues and enhanced neurogenesis are hypothesized to encompass some of the therapeutic potential of iPSCs, recent evidence has demonstrated a substantial paracrine effect on neuroinflammation. Specifically, investigation of iPSCs, iPSC-neural progenitor cells (iPSC-NPCs), and iPSC-neuroepithelial like stem cells (iPSC-lt-NESC) has demonstrated significant immunomodulation of proinflammatory signaling and endogenous inflammatory cell populations, such as microglia. This review aims to examine the mechanisms by which iPSCs mediate neuroinflammation in the post-stroke environment, as well as delineate avenues for further investigation.
topic induced pluripotent stem cells
stroke
iNSCs
neuroinflammation
stem cells
url https://www.frontiersin.org/articles/10.3389/fcell.2021.647415/full
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