The effect of miR-1338 on the immunomodulatory activity of ophiopogon polysaccharide liposome.
Immunomodulatory activity
Kupffer cells
Ophiopogon polysaccharide liposome
TLR4-NF-κB signaling pathway
microRNA-1338
Journal
International journal of biological macromolecules
ISSN: 1879-0003
Titre abrégé: Int J Biol Macromol
Pays: Netherlands
ID NLM: 7909578
Informations de publication
Date de publication:
15 Dec 2021
15 Dec 2021
Historique:
received:
13
09
2021
revised:
16
10
2021
accepted:
01
11
2021
pubmed:
15
11
2021
medline:
24
12
2021
entrez:
14
11
2021
Statut:
ppublish
Résumé
This study is to investigate the effect of microRNA-1338 (miR-1338) on the activity of Kupffer cells (KCs) and its mechanism regulated by ophiopogon polysaccharide liposome (OPL). KCs was treated with different OPL after transfected with miR-1338 mimic and miR-1338 inhibitor. The secretion of NO and iNOS, the expression of catalase (CAT) and peroxidase (POD), the phagocytic activity, the expression of CD14 and MHC II, the apoptosis and the secretion of ROS were measured. In addition, the expressions of key signal factors TLR4, IKKβ, MyD88 and NF-κB in NF-κB signaling pathway were measured by real-time PCR and Western blot (WB). The results showed that OPL could promote the secretion of iNOS, the expression of POD, the phagocytosis, the mRNA expression of TLR4, MyD88, IKKβ and NF-κB, the protein expression of TLR4 and NF-κB, and inhibit the cell apoptosis and ROS secretion after transfected with miR-1338 mimic. After transfected with miR-1338 inhibitor, OPL could promote the secretion of NO and iNOS, the expression of POD, cell migration, phagocytosis, and inhibit cell apoptosis. Meanwhile, the mRNA expression of TLR4, MyD88, IKKβ and NF-κB and the protein expression of TLR4, MyD88 and NF-κB were promoted. These results suggested that OPL could activate TLR4-NF-κB signaling pathway and thereby improve the activity of KCs by regulating miR-1338.
Identifiants
pubmed: 34774589
pii: S0141-8130(21)02417-X
doi: 10.1016/j.ijbiomac.2021.11.019
pii:
doi:
Substances chimiques
Immunologic Factors
0
Liposomes
0
MicroRNAs
0
Polysaccharides
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
1871-1884Informations de copyright
Copyright © 2021 Elsevier B.V. All rights reserved.