» Articles » PMID: 39091599

Immunostimulatory Activity of the Aqueous Extract from the Leaves of Subsp. Through TLR4‑dependent JNK Activation in RAW264.7 Cells

Overview
Journal Biomed Rep
Specialty Biochemistry
Date 2024 Aug 2
PMID 39091599
Authors
Affiliations
Soon will be listed here.
Abstract

subsp. (SRP) is an endemic plant of Korea, exclusively found on Ulleungdo Island. SRP is widely used as both a traditional medicine and food source. However, there is a lack of research on the pharmacological activities of SRP. Therefore, the present study aimed to explore the potential use of SRP leaves (SRPL) as a natural immunostimulant by analyzing its macrophage activation properties and the underlying mechanisms of action. Among the various extraction conditions, SRPL (AE20-SRPL) extracted with 100% distilled water at 20˚C induced the highest nitric oxide (NO) production in RAW264.7 cells. Thus, the further studies were performed using AE20-SRPL. AE20-SRPL increased the production of immunostimulatory factors such as NO, prostaglandin E2, inducible nitric oxide synthase, cyclooxygenase-2, IL-1β and TNF-α and phagocytosis in a dose-dependent manner in RAW264.7 cells without exhibiting cytotoxicity. Among Toll-like receptor (TLR)2 and TLR4, inhibition of TLR4 significantly reduced AE20-SRPL-mediated increases in the production of immunostimulatory factors and phagocytosis in RAW264.7 cells. Furthermore, in RAW264.7 cells, inhibition of JNK, one of the components of MAPK signaling along with ERK1/2 and p38, attenuated the AE20-SRPL-mediated increases in the production of immunostimulatory factors and phagocytosis. Additionally, AE20-SRPL induced the phosphorylation of JNK and inhibition of TLR4 reduced AE20-SRPL-mediated JNK phosphorylation. These results suggested that AE20-SRPL may enhance the production of immunostimulatory factors and phagocytosis through TLR4-dependent activation of JNK in macrophages. Although the present study is limited to research using a cell model, AE20-SRPL demonstrated potential as a natural material capable of inducing macrophage activation for immune enhancement.

References
1.
Arango Duque G, Descoteaux A . Macrophage cytokines: involvement in immunity and infectious diseases. Front Immunol. 2014; 5:491. PMC: 4188125. DOI: 10.3389/fimmu.2014.00491. View

2.
Xie X, Tang M, Yi S, He Y, Chen S, Zhao Y . Polysaccharide of Asparagus cochinchinensis (Lour.) Merr regulates macrophage immune response and epigenetic memory through TLR4-JNK/p38/ERK signaling pathway and histone modification. Phytomedicine. 2024; 124:155294. DOI: 10.1016/j.phymed.2023.155294. View

3.
Um Y, Eo H, Kim H, Kim K, Jeon K, Jeong J . Wild simulated ginseng activates mouse macrophage, RAW264.7 cells through TRL2/4-dependent activation of MAPK, NF-κB and PI3K/AKT pathways. J Ethnopharmacol. 2020; 263:113218. DOI: 10.1016/j.jep.2020.113218. View

4.
Martinez-Colon G, Moore B . Prostaglandin E as a Regulator of Immunity to Pathogens. Pharmacol Ther. 2017; 185:135-146. PMC: 5898978. DOI: 10.1016/j.pharmthera.2017.12.008. View

5.
Beutler B, Jiang Z, Georgel P, Crozat K, Croker B, Rutschmann S . Genetic analysis of host resistance: Toll-like receptor signaling and immunity at large. Annu Rev Immunol. 2006; 24:353-89. DOI: 10.1146/annurev.immunol.24.021605.090552. View