Contemplating IL‐6, a double‐edged sword cytokine: Which side to use for stroke pathology?
Interleukin (IL)‐6 is a unique cytokine due to its dual signaling, with one pathway being pro‐inflammatory (trans) and the other homeostatic (classical). Both of these pathways have been implicated in neuroinflammation following stroke, with initial inflammatory mechanisms being protective and later...
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Published in | CNS neuroscience & therapeutics Vol. 29; no. 2; pp. 493 - 497 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
England
John Wiley & Sons, Inc
01.02.2023
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Subjects | |
Online Access | Get full text |
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Summary: | Interleukin (IL)‐6 is a unique cytokine due to its dual signaling, with one pathway being pro‐inflammatory (trans) and the other homeostatic (classical). Both of these pathways have been implicated in neuroinflammation following stroke, with initial inflammatory mechanisms being protective and later anti‐inflammatory signaling promoting ischemic tissue recovery. IL‐6 plays a major role in stroke pathology. However, given these distinctive IL‐6 signaling consequences, IL‐6 is a difficult cytokine to target for stroke therapies. Recent research suggests that the ratio between the pro‐inflammatory binary IL6:sIL6R complex and the inactive ternary IL6:sIL6R:sgp130 complex may be a novel way to measure IL‐6 signaling at different time points following ischemic injury. This ratio may approximate functional consequences on individualized stroke therapies, allowing clinicians to determine whether IL‐6 agonists or antagonists should be used at specific time points.
IL‐6 mounts a balancing act on stroke inflammation. IL‐6 employs discrete pathways that elicit divergent inflammatory responses. Interrogating the role of exogenous sgp130 may lead to optimal modulation of the inflammatory signaling pathway, allowing IL‐6 to exert therapeutic effects in stroke. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-3 content type line 23 ObjectType-Review-2 |
ISSN: | 1755-5930 1755-5949 |
DOI: | 10.1111/cns.14041 |