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Egr-1 is a key regulator of the blood-brain barrier damage induced by meningitic Escherichia coli

Ruicheng Yang, Xinyi Wang, Xinyi Wang, Jiaqi Chen, Chen Tan, Huanchun Chen, Xiangru Wang, Xiangru Wang, Xiangru Wang

2024Cell Communication and Signaling22 citationsDOIOpen Access PDF

Abstract

Bacterial meningitis remains a leading cause of infection-related mortality worldwide. Although Escherichia coli (E. coli) is the most common etiology of neonatal meningitis, the underlying mechanisms governing bacterial blood-brain barrier (BBB) disruption during infection remain elusive. We observed that infection of human brain microvascular endothelial cells with meningitic E. coli triggers the activation of early growth response 1 (Egr-1), a host transcriptional activator. Through integrated chromatin immunoprecipitation sequencing and transcriptome analysis, we identified Egr-1 as a crucial regulator for maintaining BBB integrity. Mechanistically, Egr-1 induced cytoskeletal changes and downregulated tight junction protein expression by directly targeting VEGFA, PDGFB, and ANGPTL4, resulting in increased BBB permeability. Meanwhile, Egr-1 also served as a master regulator in the initiation of neuroinflammatory response during meningitic E. coli infection. Our findings support an Egr-1-dependent mechanism of BBB disruption by meningitic E. coli, highlighting a promising therapeutic target for bacterial meningitis.

Topics & Concepts

Blood–brain barrierEscherichia coliTight junctionChromatin immunoprecipitationTranscriptomeMicrobiologyNeuroinflammationRegulatorMeningitisBiologyMedicineCell biologyImmunologyInflammationNeuroscienceCentral nervous systemGene expressionBiochemistryGenePromoterPsychiatryBarrier Structure and Function StudiesDrug Transport and Resistance MechanismsCaveolin-1 and cellular processes