Reduction of Pro-inflammatory Markers in RAW264.7 Macrophages by Polyethylenimines.
Anti-inflammatory properties
Lipopolysaccharide
cationic polymer
immune modulation
macrophages
polyethylenimine
Journal
Macromolecular bioscience
ISSN: 1616-5195
Titre abrégé: Macromol Biosci
Pays: Germany
ID NLM: 101135941
Informations de publication
Date de publication:
28 Feb 2024
28 Feb 2024
Historique:
revised:
31
01
2024
received:
27
10
2023
medline:
28
2
2024
pubmed:
28
2
2024
entrez:
28
2
2024
Statut:
aheadofprint
Résumé
The physiological problem of chronic inflammation and its associated pathologies attract ongoing attention with regard to methods for their control. Current systemic pharmacological treatments present problematic side effects. Thus, the possibility of new anti-inflammatory compounds with differing mechanisms of action or biophysical properties is enticing. Cationic polymers, with their ability to act as carriers for other molecules or to form bio-compatible materials, present one such possibility. Although not well described, several polycations such as chitosan and polyarginine, have displayed anti-inflammatory properties. The present work shows the ubiquitous laboratory transfection reagent, polyethylenimine (PEI) and more specifically low molecular weight branched PEI as also possessing such properties. Using a RAW264.7 murine cell line macrophage as an inflammation model, it was found the B-PEI 700 Da as being capable of reducing the production of several pro-inflammatory molecules induced by the endotoxin lipopolysaccharide. Although further studies are required for elucidation of its mechanisms, the revelation that such a common lab reagent may present these effects has wide-ranging implications, as well as an abundance of possibilities. This article is protected by copyright. All rights reserved.
Identifiants
pubmed: 38414380
doi: 10.1002/mabi.202300492
doi:
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
e2300492Informations de copyright
This article is protected by copyright. All rights reserved.