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Research progress of the CXCR4 mechanism in Alzheimer's disease
Alzheimer's disease (AD) is a degenerative brain disease with complex clinical manifestations and pathogeneses such as abnormal deposition of beta‐amyloid protein and inflammation caused by the excessive activation of microglia. CXC motif chemokine receptor type 4 (CXCR4) is a type of G protein...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10528775/ https://www.ncbi.nlm.nih.gov/pubmed/37786419 http://dx.doi.org/10.1002/ibra.12026 |
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author | Wang, Qiu‐Lin Fang, Chang‐Le Huang, Xue‐Yan Xue, Lu‐Lu |
author_facet | Wang, Qiu‐Lin Fang, Chang‐Le Huang, Xue‐Yan Xue, Lu‐Lu |
author_sort | Wang, Qiu‐Lin |
collection | PubMed |
description | Alzheimer's disease (AD) is a degenerative brain disease with complex clinical manifestations and pathogeneses such as abnormal deposition of beta‐amyloid protein and inflammation caused by the excessive activation of microglia. CXC motif chemokine receptor type 4 (CXCR4) is a type of G protein‐coupled receptor that binds to CXC motif ligand 12 (CXCL12) to activate downstream signaling pathways, such as the Janus kinase/signal transducer and activator of transcription and the renin–angiotensin system (Ras)/RAF proto‐oncogene serine (Raf)/mitogen‐activated protein kinase/extracellular‐regulated protein kinase; most of these signaling pathways are involved in inflammatory responses. CXCR4 is highly expressed in the microglia and astrocytes; this might be one of the important causes of inflammation caused by microglia and astrocytes. In this review, we summarize the mechanism and therapeutics of AD, the structures of CXCR4 and the CXCL12 ligand, and the mechanisms of CXCR4/CXCL12 that are involved in the occurrence and development of AD. The possible treatment of AD through microglia and astrocytes is also discussed, with the aim of providing a new method for the treatment of AD. |
format | Online Article Text |
id | pubmed-10528775 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-105287752023-10-02 Research progress of the CXCR4 mechanism in Alzheimer's disease Wang, Qiu‐Lin Fang, Chang‐Le Huang, Xue‐Yan Xue, Lu‐Lu Ibrain Reviews Alzheimer's disease (AD) is a degenerative brain disease with complex clinical manifestations and pathogeneses such as abnormal deposition of beta‐amyloid protein and inflammation caused by the excessive activation of microglia. CXC motif chemokine receptor type 4 (CXCR4) is a type of G protein‐coupled receptor that binds to CXC motif ligand 12 (CXCL12) to activate downstream signaling pathways, such as the Janus kinase/signal transducer and activator of transcription and the renin–angiotensin system (Ras)/RAF proto‐oncogene serine (Raf)/mitogen‐activated protein kinase/extracellular‐regulated protein kinase; most of these signaling pathways are involved in inflammatory responses. CXCR4 is highly expressed in the microglia and astrocytes; this might be one of the important causes of inflammation caused by microglia and astrocytes. In this review, we summarize the mechanism and therapeutics of AD, the structures of CXCR4 and the CXCL12 ligand, and the mechanisms of CXCR4/CXCL12 that are involved in the occurrence and development of AD. The possible treatment of AD through microglia and astrocytes is also discussed, with the aim of providing a new method for the treatment of AD. John Wiley and Sons Inc. 2022-03-03 /pmc/articles/PMC10528775/ /pubmed/37786419 http://dx.doi.org/10.1002/ibra.12026 Text en © 2022 The Authors. Ibrain published by Affiliated Hospital of Zunyi Medical University (AHZMU) and Wiley‐VCH GmbH. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Reviews Wang, Qiu‐Lin Fang, Chang‐Le Huang, Xue‐Yan Xue, Lu‐Lu Research progress of the CXCR4 mechanism in Alzheimer's disease |
title | Research progress of the CXCR4 mechanism in Alzheimer's disease |
title_full | Research progress of the CXCR4 mechanism in Alzheimer's disease |
title_fullStr | Research progress of the CXCR4 mechanism in Alzheimer's disease |
title_full_unstemmed | Research progress of the CXCR4 mechanism in Alzheimer's disease |
title_short | Research progress of the CXCR4 mechanism in Alzheimer's disease |
title_sort | research progress of the cxcr4 mechanism in alzheimer's disease |
topic | Reviews |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10528775/ https://www.ncbi.nlm.nih.gov/pubmed/37786419 http://dx.doi.org/10.1002/ibra.12026 |
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