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Hauptverfasser: Chen, Chun-Yu, Kuo, Yu-Ting, Liaw, Chih-Chuang, Wang, Yi-Hsuan, Chang, Shih-Hsin, Tsai, Yung-Fong, Hsu, Kai-Cheng, Lin, Tony Eight, Hwang, Tsong-Long
Format: Artículo científico
Sprache:en
Veröffentlicht: Biochemical pharmacology 2025
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Online-Zugang:https://pubmed.ncbi.nlm.nih.gov/40987405/
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author Chen, Chun-Yu
Kuo, Yu-Ting
Liaw, Chih-Chuang
Wang, Yi-Hsuan
Chang, Shih-Hsin
Tsai, Yung-Fong
Hsu, Kai-Cheng
Lin, Tony Eight
Hwang, Tsong-Long
author_facet Chen, Chun-Yu
Kuo, Yu-Ting
Liaw, Chih-Chuang
Wang, Yi-Hsuan
Chang, Shih-Hsin
Tsai, Yung-Fong
Hsu, Kai-Cheng
Lin, Tony Eight
Hwang, Tsong-Long
Chen, Chun-Yu
Kuo, Yu-Ting
Liaw, Chih-Chuang
Wang, Yi-Hsuan
Chang, Shih-Hsin
Tsai, Yung-Fong
Hsu, Kai-Cheng
Lin, Tony Eight
Hwang, Tsong-Long
collection PubMed - marine biology
contents Butyrolactone I from Aspergillus fungi blocks neutrophil FPR1 to alleviate acute respiratory distress syndrome. Chen, Chun-Yu Kuo, Yu-Ting Liaw, Chih-Chuang Wang, Yi-Hsuan Chang, Shih-Hsin Tsai, Yung-Fong Hsu, Kai-Cheng Lin, Tony Eight Hwang, Tsong-Long Receptors, Formyl Peptide Respiratory Distress Syndrome Animals Neutrophils Humans Mice Aspergillus 4-Butyrolactone Male Mice, Inbred C57BL Formyl peptide receptor 1 (FPR1), activated by N-formyl peptides, significantly contributes to neutrophil activation and the development of acute respiratory distress syndrome (ARDS). This study showed that butyrolactone I (BLI), a secondary metabolite of Aspergillus terreus, effectively blocks FPR1 and reduces the severity of ARDS. BLI selectively inhibited superoxide anion production, elastase release, cluster of differentiation molecule 11b (CD11b) expression, and chemotaxis in human neutrophils activated by N-formyl peptides derived from bacteria and mitochondria. The FPR1 receptor-binding and molecular docking assays confirmed that BLI acted as an FPR1 inhibitor. Pharmacological experiments demonstrated that BLI selectively inhibited FPR1 downstream signals in human neutrophils, including calcium mobilization and phosphorylation of protein kinase B (Akt), c-Jun N-terminal kinases (JNK), extracellular regulated protein kinases (ERK), and p38 mitogen-activated protein kinases (p38). In a mouse model of ARDS, treatment with BLI reduced neutrophil infiltration, oxidative damage, and levels of elastase and interleukin-1 beta (IL-1β) in the lungs. The fungal compound BLI could serve as a potential treatment for ARDS by blocking FPR1 and reducing neutrophil-induced injury.
format Artículo científico
id pubmed_40987405
institution PubMed
language en
publishDate 2025
publisher Biochemical pharmacology
record_format pubmed
spellingShingle Butyrolactone I from Aspergillus fungi blocks neutrophil FPR1 to alleviate acute respiratory distress syndrome.
Chen, Chun-Yu
Kuo, Yu-Ting
Liaw, Chih-Chuang
Wang, Yi-Hsuan
Chang, Shih-Hsin
Tsai, Yung-Fong
Hsu, Kai-Cheng
Lin, Tony Eight
Hwang, Tsong-Long
Receptors, Formyl Peptide
Respiratory Distress Syndrome
Animals
Neutrophils
Humans
Mice
Aspergillus
4-Butyrolactone
Male
Mice, Inbred C57BL
Butyrolactone I from Aspergillus fungi blocks neutrophil FPR1 to alleviate acute respiratory distress syndrome. Chen, Chun-Yu Kuo, Yu-Ting Liaw, Chih-Chuang Wang, Yi-Hsuan Chang, Shih-Hsin Tsai, Yung-Fong Hsu, Kai-Cheng Lin, Tony Eight Hwang, Tsong-Long Receptors, Formyl Peptide Respiratory Distress Syndrome Animals Neutrophils Humans Mice Aspergillus 4-Butyrolactone Male Mice, Inbred C57BL Formyl peptide receptor 1 (FPR1), activated by N-formyl peptides, significantly contributes to neutrophil activation and the development of acute respiratory distress syndrome (ARDS). This study showed that butyrolactone I (BLI), a secondary metabolite of Aspergillus terreus, effectively blocks FPR1 and reduces the severity of ARDS. BLI selectively inhibited superoxide anion production, elastase release, cluster of differentiation molecule 11b (CD11b) expression, and chemotaxis in human neutrophils activated by N-formyl peptides derived from bacteria and mitochondria. The FPR1 receptor-binding and molecular docking assays confirmed that BLI acted as an FPR1 inhibitor. Pharmacological experiments demonstrated that BLI selectively inhibited FPR1 downstream signals in human neutrophils, including calcium mobilization and phosphorylation of protein kinase B (Akt), c-Jun N-terminal kinases (JNK), extracellular regulated protein kinases (ERK), and p38 mitogen-activated protein kinases (p38). In a mouse model of ARDS, treatment with BLI reduced neutrophil infiltration, oxidative damage, and levels of elastase and interleukin-1 beta (IL-1β) in the lungs. The fungal compound BLI could serve as a potential treatment for ARDS by blocking FPR1 and reducing neutrophil-induced injury.
title Butyrolactone I from Aspergillus fungi blocks neutrophil FPR1 to alleviate acute respiratory distress syndrome.
topic Receptors, Formyl Peptide
Respiratory Distress Syndrome
Animals
Neutrophils
Humans
Mice
Aspergillus
4-Butyrolactone
Male
Mice, Inbred C57BL
url https://pubmed.ncbi.nlm.nih.gov/40987405/