Resolving inflammation by TAM receptor activation
The control of inflammation is strictly regulated to ensure the adequate intensity and duration of an inflammatory response, enabling the removal of the trigger factors and the restoration of the integrity of the tissues and their functions. This process is coordinated by anti-inflammatory and pro-r...
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Published in: | Pharmacology & therapeutics (Oxford) Vol. 227; p. 107893 |
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Main Authors: | , , |
Format: | Journal Article |
Language: | English |
Published: |
England
Elsevier Inc
01-11-2021
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Subjects: | |
Online Access: | Get full text |
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Summary: | The control of inflammation is strictly regulated to ensure the adequate intensity and duration of an inflammatory response, enabling the removal of the trigger factors and the restoration of the integrity of the tissues and their functions. This process is coordinated by anti-inflammatory and pro-resolving mediators that regulate the cellular and molecular events necessary to restore homeostasis, and defects in this control are associated with the development of chronic and autoimmune diseases. The TAM family of receptor tyrosine kinases—Tyro3, Axl, and MerTK—plays an essential role in efferocytosis, a key process for the resolution of inflammation. However, new studies have demonstrated that TAM receptor activation not only reduces the synthesis of pro-inflammatory mediators by different cell types in response to some stimuli but also stimulates the production of anti-inflammatory and pro-resolving molecules that control the inflammation. This review provides a comprehensive view of TAM receptor family members as important players in controlling inflammatory responses through anti-inflammatory and pro-resolving actions.
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•TAM receptor family members modulate efferocytosis, macrophage polarization, and production of pro-resolving mediators.•TAM receptor family members control inflammatory responses through anti-inflammatory and pro-resolving mechanisms.•TAM receptor modulation can be a therapeutic alternative for more complex and emerging diseases. |
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Bibliography: | ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-3 content type line 23 ObjectType-Review-1 |
ISSN: | 0163-7258 1879-016X |
DOI: | 10.1016/j.pharmthera.2021.107893 |