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Electroacupuncture regulates microglia polarization via lncRNA-mediated hippo pathway after ischemic stroke.

Authors :
Chen, Shenxu
Wang, Linmei
Yuan, Ying
Wen, Yunfan
Shu, Shi
Source :
Biotechnology & Genetic Engineering Reviews; Oct2023, Vol. 39 Issue 2, p1379-1395, 17p
Publication Year :
2023

Abstract

Microglia polarization and microglia-mediated inflammation play a crucial role in the development of ischaemic brain injury. Electroacupuncture (EA) has the function of anti-inflammatory, which has been thoroughly validated and utilized to treat ischemic brain damage. The fundamental mechanism by which EA alleviates ischemic brain damage by decreasing microglia polarization and microglia-mediated inflammation, however, remains unknown. In the current study, the activation of microglia and inflammatory cytokines was analyzed to confirm the anti-inflammatory function of EA in middle cerebral artery occlusion (MCAO) rats. Whole-transcriptome sequencing was used to examine the differentially expressed lncRNAs in the control, MCAO, and MCAO +EA groups. Our findings demonstrated that EA treatment reduced microglia activation and inflammatory cytokine production. In addition, there are 44 lncRNAs were found significantly different in three groups, and the Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway of the predicted targets of these lncRNAs suggested that the Hippo pathway may contribute to the development of ischaemic brain injury and to the anti-inflammatory function of EA. Moreover, our data showed that lncRNA TCONS_00022826 (Lnc826) was upregulated in MCAO group, whereas blocked by EA treatment. Furthermore, in vitro OGD cell model data showed that Lnc826 promoted M1 polarization of microglia by regulating the Hippo pathway. Our data suggested that regulating microglia polarization via Lnc826-mediated hippo pathway is a possible mechanism of the EA treatment on ischemic brain injury. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
02648725
Volume :
39
Issue :
2
Database :
Supplemental Index
Journal :
Biotechnology & Genetic Engineering Reviews
Publication Type :
Academic Journal
Accession number :
179769188
Full Text :
https://doi.org/10.1080/02648725.2023.2177046