The C–C chemokine receptor 7: An immune molecule that modulates central nervous system function in homeostasis and disease
The interaction between the central nervous system (CNS) and the peripheral immune system is key for brain function in homeostasis and disease. Recent studies have revealed that the C–C chemokine receptor 7 (CCR7) is expressed in both CNS resident cells and peripheral immune cells, and plays an impo...
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Published in | Brain, behavior, & immunity. Health Vol. 29; p. 100610 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
Elsevier Inc
01.05.2023
Elsevier |
Subjects | |
Online Access | Get full text |
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Summary: | The interaction between the central nervous system (CNS) and the peripheral immune system is key for brain function in homeostasis and disease. Recent studies have revealed that the C–C chemokine receptor 7 (CCR7) is expressed in both CNS resident cells and peripheral immune cells, and plays an important role in regulating behavior in homeostasis and neuroinflammation in disease. This review integrates studies examining the role of CCR7 in CNS resident and peripheral immune cells in homeostasis and disease, as well as the pathways of peripheral immune cell migration in and out of the brain via CCR7. A special emphasis is placed on the CCR7-dependent migration of peripheral immune cells into the recently discovered meningeal lymphatic vessels surrounding the brain and nasal lymphatics, its migration into cervical lymph nodes, and the implications that this migration might have for CNS function.
•CCR7 modulates behavior in homeostasis.•CCR7 modulates neuroinflammation in disease states.•CCR7 supports the entry of T-cells into the CNS.•CCR7 supports the migration of dendritic and T-cells into meningeal lymphatics.•CCR7 supports antigen presentation within cervical lymph nodes. |
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Bibliography: | ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-3 content type line 23 ObjectType-Review-1 |
ISSN: | 2666-3546 2666-3546 |
DOI: | 10.1016/j.bbih.2023.100610 |