Marine-Derived Alternariol Suppresses Inflammation by Regulating T Cell Activation and Migration.

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Main Authors: Liu, Chenfeng, Gu, Fudie, Zou, Zhengbiao, Wang, Fengli, Li, Dashuai, Song, Jing, Hong, Yazhen, Wu, Xuhui, Yang, Xianwen, Liu, Wen-Hsien, Liu, Guangming, Zhou, Yu, Liu, Qingmei
Format: Artículo científico
Language:en
Published: Marine drugs 2025
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author Liu, Chenfeng
Gu, Fudie
Zou, Zhengbiao
Wang, Fengli
Li, Dashuai
Song, Jing
Hong, Yazhen
Wu, Xuhui
Yang, Xianwen
Liu, Wen-Hsien
Liu, Guangming
Zhou, Yu
Liu, Qingmei
author_facet Liu, Chenfeng
Gu, Fudie
Zou, Zhengbiao
Wang, Fengli
Li, Dashuai
Song, Jing
Hong, Yazhen
Wu, Xuhui
Yang, Xianwen
Liu, Wen-Hsien
Liu, Guangming
Zhou, Yu
Liu, Qingmei
Liu, Chenfeng
Gu, Fudie
Zou, Zhengbiao
Wang, Fengli
Li, Dashuai
Song, Jing
Hong, Yazhen
Wu, Xuhui
Yang, Xianwen
Liu, Wen-Hsien
Liu, Guangming
Zhou, Yu
Liu, Qingmei
collection PubMed - marine biology
contents Marine-Derived Alternariol Suppresses Inflammation by Regulating T Cell Activation and Migration. Liu, Chenfeng Gu, Fudie Zou, Zhengbiao Wang, Fengli Li, Dashuai Song, Jing Hong, Yazhen Wu, Xuhui Yang, Xianwen Liu, Wen-Hsien Liu, Guangming Zhou, Yu Liu, Qingmei Animals Mice Lymphocyte Activation Cell Movement Anti-Inflammatory Agents Cell Proliferation Inflammation Lactones Ovalbumin Mice, Inbred C57BL Aquatic Organisms T-Lymphocytes Cytokines Apoptosis T cells play pivotal roles in inflammation's initiation and progression. Exploring natural compounds that regulate T cell function is crucial for preventing and treating inflammation. Herein, we report that Alternariol (AOH), a marine-derived secondary metabolite, exerts an anti-inflammatory activity by targeting T cell function. Using an ovalbumin (OVA)-induced OT-II CD4 T cell activation model, we demonstrated that AOH potently suppresses T cell proliferation and cytokine secretion, mildly promotes T cell apoptosis, and spares antigen presentation processes. Mechanistically, AOH controlled early T cell activation by inhibiting the expression of activation markers (CD69, CD25, CD44) and transcription factors (T-bet, Eomes), leading to impaired Th1 cytokine production. In vivo experiments revealed that AOH attenuated OVA-induced lung injury in mice by reducing immune cell infiltration in pulmonary tissues and draining lymph nodes. Notably, AOH dramatically suppressed OVA-specific T cells migrating to the inflammatory lung while impairing T-cell-mediated other immune cell infiltration. Collectively, AOH exhibited potent anti-inflammatory effects by modulating T cell proliferation, function, and migration, offering a promising therapeutic strategy for T-cell-mediated inflammatory diseases.
format Artículo científico
id pubmed_40137319
institution PubMed
language en
publishDate 2025
publisher Marine drugs
record_format pubmed
spellingShingle Marine-Derived Alternariol Suppresses Inflammation by Regulating T Cell Activation and Migration.
Liu, Chenfeng
Gu, Fudie
Zou, Zhengbiao
Wang, Fengli
Li, Dashuai
Song, Jing
Hong, Yazhen
Wu, Xuhui
Yang, Xianwen
Liu, Wen-Hsien
Liu, Guangming
Zhou, Yu
Liu, Qingmei
Animals
Mice
Lymphocyte Activation
Cell Movement
Anti-Inflammatory Agents
Cell Proliferation
Inflammation
Lactones
Ovalbumin
Mice, Inbred C57BL
Aquatic Organisms
T-Lymphocytes
Cytokines
Apoptosis
Marine-Derived Alternariol Suppresses Inflammation by Regulating T Cell Activation and Migration. Liu, Chenfeng Gu, Fudie Zou, Zhengbiao Wang, Fengli Li, Dashuai Song, Jing Hong, Yazhen Wu, Xuhui Yang, Xianwen Liu, Wen-Hsien Liu, Guangming Zhou, Yu Liu, Qingmei Animals Mice Lymphocyte Activation Cell Movement Anti-Inflammatory Agents Cell Proliferation Inflammation Lactones Ovalbumin Mice, Inbred C57BL Aquatic Organisms T-Lymphocytes Cytokines Apoptosis T cells play pivotal roles in inflammation's initiation and progression. Exploring natural compounds that regulate T cell function is crucial for preventing and treating inflammation. Herein, we report that Alternariol (AOH), a marine-derived secondary metabolite, exerts an anti-inflammatory activity by targeting T cell function. Using an ovalbumin (OVA)-induced OT-II CD4 T cell activation model, we demonstrated that AOH potently suppresses T cell proliferation and cytokine secretion, mildly promotes T cell apoptosis, and spares antigen presentation processes. Mechanistically, AOH controlled early T cell activation by inhibiting the expression of activation markers (CD69, CD25, CD44) and transcription factors (T-bet, Eomes), leading to impaired Th1 cytokine production. In vivo experiments revealed that AOH attenuated OVA-induced lung injury in mice by reducing immune cell infiltration in pulmonary tissues and draining lymph nodes. Notably, AOH dramatically suppressed OVA-specific T cells migrating to the inflammatory lung while impairing T-cell-mediated other immune cell infiltration. Collectively, AOH exhibited potent anti-inflammatory effects by modulating T cell proliferation, function, and migration, offering a promising therapeutic strategy for T-cell-mediated inflammatory diseases.
title Marine-Derived Alternariol Suppresses Inflammation by Regulating T Cell Activation and Migration.
topic Animals
Mice
Lymphocyte Activation
Cell Movement
Anti-Inflammatory Agents
Cell Proliferation
Inflammation
Lactones
Ovalbumin
Mice, Inbred C57BL
Aquatic Organisms
T-Lymphocytes
Cytokines
Apoptosis
url https://pubmed.ncbi.nlm.nih.gov/40137319/