AI Article Synopsis

  • Lysozyme is a key player in the innate immune system, known for its antibacterial properties and emerging anti-inflammatory effects, which are still being understood.
  • A study using RNA sequencing on U937 monocyte cells revealed that lysozyme alters the expression of genes related to the TNF-α/IL-1β inflammatory pathway.
  • The findings suggest that even low concentrations of lysozyme can significantly impact gene regulation, highlighting its potential for therapeutic use in managing inflammation.

Article Abstract

Lysozyme is one of the most important anti-bacterial effectors in the innate immune system of animals. Besides its direct antibacterial enzymatic activity, lysozyme displays other biological properties, pointing toward a significant anti-inflammatory effect, many aspects of which are still elusive. Here we investigate the perturbation of gene expression profiles induced by lysozyme in a monocyte cell line in vitro considering a perspective as broad as the whole transcriptome profiling. The results of the RNA-seq experiment show that lysozyme induces transcriptional modulation of the TNF-α/IL-1β pathway genes in U937 monocytes. The analysis of transcriptomic profiles with IPA identified a simple but robust molecular network of genes, in which the regulation trends are fully consistent with the anti-inflammatory activity of lysozyme. This study provides the first evidence in support of the anti-inflammatory action of lysozyme on the basis of transcriptomic regulation data resulting from the broad perspective of a whole-transcriptome profiling. Such important effects can be achieved with the supplementation of relatively low concentrations of lysozyme, for a short time of exposure. These new insights allow the potential of lysozyme in pharmacological applications to be better exploited.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6862675PMC
http://dx.doi.org/10.3390/ijms20215502DOI Listing

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