| Literature DB >> 33613460 |
Aritra Bhattacharyya1, Toni Herta1, Claudia Conrad1, Doris Frey1, Pedro García2,3, Norbert Suttorp1, Stefan Hippenstiel1, Janine Zahlten1.
Abstract
The recruitment and activation of polymorphonuclear neutrophils (PMNs) are of central importance for the elimination of pathogens in bacterial infections. We investigated the Streptococcus pneumoniae-dependent induction of the transcription factor Krüppel-like factor (KLF) 4 in PMNs as a potential regulator of PMN activation. We found that KLF4 expression is induced in human blood-derived PMNs in a time- and dose-dependent manner by wild-type S. pneumoniae and capsule knockout mutants. Unencapsulated knockout mutants induced stronger KLF4 expression than encapsulated wild types. The presence of autolysin LytA-competent (thus viable) pneumococci and LytA-mediated bacterial autolysis were required for KLF4 induction in human and murine PMNs. LyzMcre-mediated knockdown of KLF4 in murine blood-derived PMNs revealed that KLF4 influences pneumococci killing and increases the release of the proinflammatory cytokines tumor necrosis factor α and keratinocyte chemoattractant and decreases the release of the anti-inflammatory cytokine interleukin-10. Thus, S. pneumoniae induces KLF4 expression in PMNs, which contributes to PMN activation in S. pneumoniae infection.Entities:
Keywords: Krüppel-like factor 4; S. pneumoniae; infectious diseases; innate immunity; neutrophils
Year: 2021 PMID: 33613460 PMCID: PMC7887292 DOI: 10.3389/fmicb.2020.582070
Source DB: PubMed Journal: Front Microbiol ISSN: 1664-302X Impact factor: 5.640