Journal
BIOMEDICINES
Volume 10, Issue 10, Pages -Publisher
MDPI
DOI: 10.3390/biomedicines10102358
Keywords
bacterial sepsis and meningitis; alpha7 nicotinic acetylcholine receptor; blood-brain barriers; cytokine-inducible SH2-containing protein
Categories
Funding
- National Natural Science Foundation of China [81871198]
- National Science Foundation for Young Scientists of China [81801985]
- Scientific Research Enlightenment Plan of Southern Medical University [B219339044]
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Excessive antibiotic treatments for bacterial sepsis and meningitis in children may have adverse outcomes. The alpha 7nAChR/CISH/JAK2/STAT5 axis plays a critical role in the pathogenesis of E. coli-induced brain microvascular leakage and blood-brain barrier disruptions. Alpha 7nAChR antagonists show potential in protecting against HBMECs injuries and BBB disruptions.
Despite the availability of antibiotics over the last several decades, excessive antibiotic treatments for bacterial sepsis and meningitis (BSM) in children may result in several adverse outcomes. Hematogenous pathogens may directly induce permeability increases in human brain microvascular endothelial cells (HBMECs) and blood-brain barrier (BBB) dysfunctions. Our preliminary studies demonstrated that the alpha7 nicotinic acetylcholine receptor (alpha 7nAChR) played an important role in the pathogenesis of BSM, accompanied by increasing cytokine-inducible SH2-containing protein (CISH) at the transcriptome level, but it has remained unclear how alpha 7nAChR-CISH works mechanistically. The study aims to explore the underlying mechanism of alpha 7nAChR and CISH during E. coli-induced BSM in vitro (HBMECs) and in vivo (alpha 7nAChR-KO mouse). We found that in the stage of E. coli K1-induced BBB disruptions, alpha 7nAChR functioned as the key regulator that affects the integrity of HBMECs by activating the JAK2-STAT5 signaling pathway, while CISH inhibited JAK2-STAT5 activation and exhibited protective effects against E. coli infection. Notably, we first validated that the expression of CISH could be regulated by alpha 7nAChR in HBMECs. In addition, we determined the protective effects of MLA (methyllycaconitine citrate) and MEM (memantine hydrochloride) (functioning as alpha 7nAChR antagonists) on infected HBMECs and suggested that the alpha 7nAChR-CISH axis could explain the protective effects of the two small-molecule compounds on E. coli-induced HBMECs injuries and BBB disruptions. In conclusion, we dissected the alpha 7nAChR/CISH/JAK2/STAT5 axis as critical for the pathogenesis of E. coli-induced brain microvascular leakage and BBB disruptions and provided novel evidence for the development of alpha 7nAChR antagonists in the prevention of pediatric E. coli BSM.
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