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Significance of Complement System in Ischemic Stroke: A Comprehensive Review
The complement system is an essential part of innate immunity, typically conferring protection via eliminating pathogens and accumulating debris. However, the defensive function of the complement system can exacerbate immune, inflammatory, and degenerative responses in various pathological condition...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
JKL International LLC
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6457046/ https://www.ncbi.nlm.nih.gov/pubmed/31011487 http://dx.doi.org/10.14336/AD.2019.0119 |
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author | Ma, Yuanyuan Liu, Yanqun Zhang, Zhijun Yang, Guo-Yuan |
author_facet | Ma, Yuanyuan Liu, Yanqun Zhang, Zhijun Yang, Guo-Yuan |
author_sort | Ma, Yuanyuan |
collection | PubMed |
description | The complement system is an essential part of innate immunity, typically conferring protection via eliminating pathogens and accumulating debris. However, the defensive function of the complement system can exacerbate immune, inflammatory, and degenerative responses in various pathological conditions. Cumulative evidence indicates that the complement system plays a critical role in the pathogenesis of ischemic brain injury, as the depletion of certain complement components or the inhibition of complement activation could reduce ischemic brain injury. Although multiple candidates modulating or inhibiting complement activation show massive potential for the treatment of ischemic stroke, the clinical availability of complement inhibitors remains limited. The complement system is also involved in neural plasticity and neurogenesis during cerebral ischemia. Thus, unexpected side effects could be induced if the systemic complement system is inhibited. In this review, we highlighted the recent concepts and discoveries of the roles of different kinds of complement components, such as C3a, C5a, and their receptors, in both normal brain physiology and the pathophysiology of brain ischemia. In addition, we comprehensively reviewed the current development of complement-targeted therapy for ischemic stroke and discussed the challenges of bringing these therapies into the clinic. The design of future experiments was also discussed to better characterize the role of complement in both tissue injury and recovery after cerebral ischemia. More studies are needed to elucidate the molecular and cellular mechanisms of how complement components exert their functions in different stages of ischemic stroke to optimize the intervention of targeting the complement system. |
format | Online Article Text |
id | pubmed-6457046 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | JKL International LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-64570462019-04-22 Significance of Complement System in Ischemic Stroke: A Comprehensive Review Ma, Yuanyuan Liu, Yanqun Zhang, Zhijun Yang, Guo-Yuan Aging Dis Review The complement system is an essential part of innate immunity, typically conferring protection via eliminating pathogens and accumulating debris. However, the defensive function of the complement system can exacerbate immune, inflammatory, and degenerative responses in various pathological conditions. Cumulative evidence indicates that the complement system plays a critical role in the pathogenesis of ischemic brain injury, as the depletion of certain complement components or the inhibition of complement activation could reduce ischemic brain injury. Although multiple candidates modulating or inhibiting complement activation show massive potential for the treatment of ischemic stroke, the clinical availability of complement inhibitors remains limited. The complement system is also involved in neural plasticity and neurogenesis during cerebral ischemia. Thus, unexpected side effects could be induced if the systemic complement system is inhibited. In this review, we highlighted the recent concepts and discoveries of the roles of different kinds of complement components, such as C3a, C5a, and their receptors, in both normal brain physiology and the pathophysiology of brain ischemia. In addition, we comprehensively reviewed the current development of complement-targeted therapy for ischemic stroke and discussed the challenges of bringing these therapies into the clinic. The design of future experiments was also discussed to better characterize the role of complement in both tissue injury and recovery after cerebral ischemia. More studies are needed to elucidate the molecular and cellular mechanisms of how complement components exert their functions in different stages of ischemic stroke to optimize the intervention of targeting the complement system. JKL International LLC 2019-04-01 /pmc/articles/PMC6457046/ /pubmed/31011487 http://dx.doi.org/10.14336/AD.2019.0119 Text en Copyright: © 2019 Ma et al. http://creativecommons.org/licenses/by/2.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed. |
spellingShingle | Review Ma, Yuanyuan Liu, Yanqun Zhang, Zhijun Yang, Guo-Yuan Significance of Complement System in Ischemic Stroke: A Comprehensive Review |
title | Significance of Complement System in Ischemic Stroke: A Comprehensive Review |
title_full | Significance of Complement System in Ischemic Stroke: A Comprehensive Review |
title_fullStr | Significance of Complement System in Ischemic Stroke: A Comprehensive Review |
title_full_unstemmed | Significance of Complement System in Ischemic Stroke: A Comprehensive Review |
title_short | Significance of Complement System in Ischemic Stroke: A Comprehensive Review |
title_sort | significance of complement system in ischemic stroke: a comprehensive review |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6457046/ https://www.ncbi.nlm.nih.gov/pubmed/31011487 http://dx.doi.org/10.14336/AD.2019.0119 |
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