Targeting CX3CR1 Signaling Dynamics: A Critical Determinant in the Temporal Regulation of Post-Stroke Neurorepair
Ischemic stroke ranks among the top global causes of disability and mortality, with a highly dynamic pathological process. Post-stroke neuroinflammation, mediated by microglia, demonstrates a dual role in both injury and repair. The CX3CR1/CX3CL1 signaling axis, highly expressed in microglia, acts a...
Saved in:
Main Authors: | , , |
---|---|
Format: | Article |
Language: | English |
Published: |
MDPI AG
2025-07-01
|
Series: | Brain Sciences |
Subjects: | |
Online Access: | https://www.mdpi.com/2076-3425/15/7/759 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
_version_ | 1839616346055245824 |
---|---|
author | Quan He Tong Zhou Quanwei He |
author_facet | Quan He Tong Zhou Quanwei He |
author_sort | Quan He |
collection | DOAJ |
description | Ischemic stroke ranks among the top global causes of disability and mortality, with a highly dynamic pathological process. Post-stroke neuroinflammation, mediated by microglia, demonstrates a dual role in both injury and repair. The CX3CR1/CX3CL1 signaling axis, highly expressed in microglia, acts as a key regulator. This review examines the spatiotemporal dynamics of the axis across the stroke process and its involvement in neural repair. Crucially, this signaling pathway demonstrates stage-dependent functional duality: its cellular sources, receptor expression profiles, and functional consequences undergo temporally orchestrated shifts, manifesting coexisting or interconverting protective and damaging properties. Ignoring this dynamism compromises the therapeutic efficacy of targeted interventions. Thus, we propose a triple precision strategy of “stroke phase—biomarker—targeted intervention”. It uses specific biomarkers for precise staging and designs interventions based on each phase’s signaling characteristics. Despite challenges like biomarker validation, mechanistic exploration, and cross-species differences, integrating cutting-edge technologies such as spatial metabolomics and AI-driven dynamic modeling promises to shift stroke therapy toward personalized spatiotemporal programming. Temporally targeting CX3CR1 signaling may offer a key basis for developing next-generation precision neural repair strategies for stroke. |
format | Article |
id | doaj-art-6c6a86320d2b49b9ab6773afceb8f50d |
institution | Matheson Library |
issn | 2076-3425 |
language | English |
publishDate | 2025-07-01 |
publisher | MDPI AG |
record_format | Article |
series | Brain Sciences |
spelling | doaj-art-6c6a86320d2b49b9ab6773afceb8f50d2025-07-25T13:17:09ZengMDPI AGBrain Sciences2076-34252025-07-0115775910.3390/brainsci15070759Targeting CX3CR1 Signaling Dynamics: A Critical Determinant in the Temporal Regulation of Post-Stroke NeurorepairQuan He0Tong Zhou1Quanwei He2Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, ChinaDepartment of Neurology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430022, ChinaDepartment of Neurology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430022, ChinaIschemic stroke ranks among the top global causes of disability and mortality, with a highly dynamic pathological process. Post-stroke neuroinflammation, mediated by microglia, demonstrates a dual role in both injury and repair. The CX3CR1/CX3CL1 signaling axis, highly expressed in microglia, acts as a key regulator. This review examines the spatiotemporal dynamics of the axis across the stroke process and its involvement in neural repair. Crucially, this signaling pathway demonstrates stage-dependent functional duality: its cellular sources, receptor expression profiles, and functional consequences undergo temporally orchestrated shifts, manifesting coexisting or interconverting protective and damaging properties. Ignoring this dynamism compromises the therapeutic efficacy of targeted interventions. Thus, we propose a triple precision strategy of “stroke phase—biomarker—targeted intervention”. It uses specific biomarkers for precise staging and designs interventions based on each phase’s signaling characteristics. Despite challenges like biomarker validation, mechanistic exploration, and cross-species differences, integrating cutting-edge technologies such as spatial metabolomics and AI-driven dynamic modeling promises to shift stroke therapy toward personalized spatiotemporal programming. Temporally targeting CX3CR1 signaling may offer a key basis for developing next-generation precision neural repair strategies for stroke.https://www.mdpi.com/2076-3425/15/7/759CX3CR1ischemic strokeCX3CL1/CX3CR1 axisCX3CL1microglianeurorepair |
spellingShingle | Quan He Tong Zhou Quanwei He Targeting CX3CR1 Signaling Dynamics: A Critical Determinant in the Temporal Regulation of Post-Stroke Neurorepair Brain Sciences CX3CR1 ischemic stroke CX3CL1/CX3CR1 axis CX3CL1 microglia neurorepair |
title | Targeting CX3CR1 Signaling Dynamics: A Critical Determinant in the Temporal Regulation of Post-Stroke Neurorepair |
title_full | Targeting CX3CR1 Signaling Dynamics: A Critical Determinant in the Temporal Regulation of Post-Stroke Neurorepair |
title_fullStr | Targeting CX3CR1 Signaling Dynamics: A Critical Determinant in the Temporal Regulation of Post-Stroke Neurorepair |
title_full_unstemmed | Targeting CX3CR1 Signaling Dynamics: A Critical Determinant in the Temporal Regulation of Post-Stroke Neurorepair |
title_short | Targeting CX3CR1 Signaling Dynamics: A Critical Determinant in the Temporal Regulation of Post-Stroke Neurorepair |
title_sort | targeting cx3cr1 signaling dynamics a critical determinant in the temporal regulation of post stroke neurorepair |
topic | CX3CR1 ischemic stroke CX3CL1/CX3CR1 axis CX3CL1 microglia neurorepair |
url | https://www.mdpi.com/2076-3425/15/7/759 |
work_keys_str_mv | AT quanhe targetingcx3cr1signalingdynamicsacriticaldeterminantinthetemporalregulationofpoststrokeneurorepair AT tongzhou targetingcx3cr1signalingdynamicsacriticaldeterminantinthetemporalregulationofpoststrokeneurorepair AT quanweihe targetingcx3cr1signalingdynamicsacriticaldeterminantinthetemporalregulationofpoststrokeneurorepair |