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Abstract TP21: The Role Of Interleukin-1α Cytokine In Poststroke Inflammation

医学 冲程(发动机) 小胶质细胞 炎症 细胞因子 白细胞介素6 白细胞介素 免疫学 脑缺血 缺血 内科学 机械工程 工程类
作者
Eloïse Lemarchand,Blake Ouvrier,Abir A. Rahman,Raymond Wong,Amruta Narayanappa,Timothy E. Gressett,Emmanuel Pinteaux,Gregory Bix
出处
期刊:Stroke [Lippincott Williams & Wilkins]
卷期号:53 (Suppl_1)
标识
DOI:10.1161/str.53.suppl_1.tp21
摘要

Stroke remains the second leading cause of death globally, with a total of 5.5 million deaths in 2016 and an estimated global lifetime risk of stroke for those aged 25 years or older at 24.9%. A key feature of stroke and poststroke injury is the inflammatory response, which is driven by a variety of pro-inflammatory cytokines to include interleukin-1 (IL-1). Evidence from pre-clinical studies have demonstrated a deleterious effect of IL-1 poststroke with a beneficial effect observed after blocking IL-1 in both pre-clinical and clinical settings. The IL-1 family has both IL-1β and IL-1α forms, and although IL-1β has been most closely studied, the distinct roles of both IL-1 isoforms during poststroke inflammation is largely unknown. In this study, we examined the contribution of IL-1α in ischemic stroke. We characterized the spatio-temporal effect of IL-1 in the brain after stroke using an in vivo model of middle cerebral artery thrombosis in an inducible IL-1α knockout mouse through topical application of FeCl3. We found that IL-1α precedes IL-1β expression after ischemic stroke and is restricted to microglia whereas IL-1β is expressed by both neutrophils and microglia. Intriguingly, microglial IL-1α deletion does not influence brain damage after ischemic stroke, and furthermore does not influence cerebral blood flow or neutrophil infiltration and IL-1β expression up to 24h after ischemic stroke. Pathway analysis following RNAseq suggests that microglial IL-1α regulates neuronal activity through CREB signaling. In vitro studies in Neuro2a (N2a) murine cell line additionally show neuronal activity regulation through CREB signaling via microglial IL-1α after oxygen glucose deprivation and reperfusion (OGD/R) model of stroke. As the role of IL-1α in stroke has yet to be fully elucidated, future experiments using both murine and in vitro models will clarify the role that IL-1α has in the pathogenesis of stroke and its relevance to inflammatory features posttroke, which may lead to future therapeutic insight.

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