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CX3CL1/CX3CR1 in Alzheimer's Disease: A Target for Neuroprotection
CX3C chemokine ligand 1 (CX3CL1) is an intriguing chemokine belonging to the CX3C family. CX3CL1 is secreted by neurons and plays an important role in modulating glial activation in the central nervous system after binding to its sole receptor CX3CR1 which mainly is expressed on microglia. Emerging...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4939332/ https://www.ncbi.nlm.nih.gov/pubmed/27429982 http://dx.doi.org/10.1155/2016/8090918 |
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author | Chen, Peiqing Zhao, Wenjuan Guo, Yanjie Xu, Juan Yin, Ming |
author_facet | Chen, Peiqing Zhao, Wenjuan Guo, Yanjie Xu, Juan Yin, Ming |
author_sort | Chen, Peiqing |
collection | PubMed |
description | CX3C chemokine ligand 1 (CX3CL1) is an intriguing chemokine belonging to the CX3C family. CX3CL1 is secreted by neurons and plays an important role in modulating glial activation in the central nervous system after binding to its sole receptor CX3CR1 which mainly is expressed on microglia. Emerging data highlights the beneficial potential of CX3CL1-CX3CR1 in the pathogenesis of Alzheimer's disease (AD), a common progressive neurodegenerative disease, and in the progression of which neuroinflammation plays a vital role. Even so, the importance of CX3CL1/CX3CR1 in AD is still controversial and needs further clarification. In this review, we make an attempt to present a concise map of CX3CL1-CX3CR1 associated with AD to find biomarkers for early diagnosis or therapeutic interventions. |
format | Online Article Text |
id | pubmed-4939332 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-49393322016-07-17 CX3CL1/CX3CR1 in Alzheimer's Disease: A Target for Neuroprotection Chen, Peiqing Zhao, Wenjuan Guo, Yanjie Xu, Juan Yin, Ming Biomed Res Int Review Article CX3C chemokine ligand 1 (CX3CL1) is an intriguing chemokine belonging to the CX3C family. CX3CL1 is secreted by neurons and plays an important role in modulating glial activation in the central nervous system after binding to its sole receptor CX3CR1 which mainly is expressed on microglia. Emerging data highlights the beneficial potential of CX3CL1-CX3CR1 in the pathogenesis of Alzheimer's disease (AD), a common progressive neurodegenerative disease, and in the progression of which neuroinflammation plays a vital role. Even so, the importance of CX3CL1/CX3CR1 in AD is still controversial and needs further clarification. In this review, we make an attempt to present a concise map of CX3CL1-CX3CR1 associated with AD to find biomarkers for early diagnosis or therapeutic interventions. Hindawi Publishing Corporation 2016 2016-06-27 /pmc/articles/PMC4939332/ /pubmed/27429982 http://dx.doi.org/10.1155/2016/8090918 Text en Copyright © 2016 Peiqing Chen et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Review Article Chen, Peiqing Zhao, Wenjuan Guo, Yanjie Xu, Juan Yin, Ming CX3CL1/CX3CR1 in Alzheimer's Disease: A Target for Neuroprotection |
title | CX3CL1/CX3CR1 in Alzheimer's Disease: A Target for Neuroprotection |
title_full | CX3CL1/CX3CR1 in Alzheimer's Disease: A Target for Neuroprotection |
title_fullStr | CX3CL1/CX3CR1 in Alzheimer's Disease: A Target for Neuroprotection |
title_full_unstemmed | CX3CL1/CX3CR1 in Alzheimer's Disease: A Target for Neuroprotection |
title_short | CX3CL1/CX3CR1 in Alzheimer's Disease: A Target for Neuroprotection |
title_sort | cx3cl1/cx3cr1 in alzheimer's disease: a target for neuroprotection |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4939332/ https://www.ncbi.nlm.nih.gov/pubmed/27429982 http://dx.doi.org/10.1155/2016/8090918 |
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