Cell Death & DiseaseImmunologyPeer-reviewed journal article
Cortical microinfarcts potentiate recurrent ischemic injury through NLRP3-dependent trained immunity
Y. Feng, T. Wu, Y. Feng, F. Liang, G. Li, Y. LiiD, Y. GuaniD, S. Liu, Y. Zhang, G. Xu, P. Zhong
Abstract
Microinfarcts are common among the elderly, and patients with microinfarcts are more vulnerable to another stroke. However, the potential effect of microinfarct on recurrent stroke remains elusive. In this study, we investigated the detrimental effect of microinfarct on recurrent stroke in mice. Microinfarct was induced using two-photon laser and photothrombotic stroke was induced in the cortex contralateral to microinfarct four weeks later. We found that CMI could trigger the formation of innate immune memory, which exacerbated the pro-inflammatory response and ischemic injury in second photothrombotic stroke. Furthermore, we clarified the role of NLRP3 inflammasome in the nuclei of microglia, which interacts with the MLL1 complex and thereby increases H3K4 methylation, suggesting that NLRP3 is critical in microinfarct-induced innate immune memory. Additionally, NLRP3 knockout in microglia attenuated microinfarct-induced detrimental effects on recurrent stroke. Our study highlights the detrimental effect of trained immunity on the recurrent stroke and reveals the important role of NLRP3 in mediating the formation of this memory, which may be a therapeutic target to mitigate recurrent strokes.
- organism: mouse
- assay: CITE-seq
- assay: proteomics
- research focus: host-pathogen & immune response
- research focus: cell signaling & trafficking
- research focus: differential expression
- approach: experimental assay
- approach: genetic perturbation / CRISPR
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