{"title":"真菌来源的细胞保护化合物拟盘多喹诺A的作用机制及抗炎活性研究","authors":"Yukine Tsurukawa, , , Yumi Katayama, , , Kazuki Kanno, , , Kanna Sato, , , Yuka Suzuki, , , Hironobu Murakami, , , Shiro Takeda, , , Motoharu Sakaue, , , Kazuyuki Sogawa, , , Yo Shinoda, , , Masaki Nagane, , , Naoyuki Aihara, , and , Shinji Kamisuki*, ","doi":"10.1021/acsomega.5c08189","DOIUrl":null,"url":null,"abstract":"<p >Pestalotioquinol A (pesA) is a novel cytoprotective natural compound previously discovered among <i>Pestalotiopsis microspora</i> metabolites. PesA protects PC12 cells against cell death induced by a peroxynitrite donor, a reactive nitrogen species (RNS). In this study, we analyzed the mechanism of action of pesA and aimed to identify its target proteins. We revealed that the cytoprotective activity of pesA was specific to RNS, such as peroxynitrite and nitric oxide. A cellular thermal shift assay (CETSA) revealed elongation factor 1-α1 (EF1α1) as a potential pesA-binding protein. Cilostazol targeting EF1α1 displayed cytoprotective activity similar to pesA. EF1α1 knockdown increased peroxynitrite sensitivity and reduced the protective activity of pesA, suggesting that EF1α1 serves as a potential target. As RNSs are linked to inflammation, we examined the anti-inflammatory activity of pesA. PesA inhibited lipopolysaccharide-stimulated proinflammatory cytokine production in RAW264.7 cells. In an inflammatory bowel disease model mice, pesA significantly suppressed colon shortening and ameliorated total histopathological scores. PesA could help elucidate RNS-related events and serve as a lead compound for developing anti-inflammatory agents.</p>","PeriodicalId":22,"journal":{"name":"ACS Omega","volume":"10 41","pages":"49243–49251"},"PeriodicalIF":4.3000,"publicationDate":"2025-10-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://pubs.acs.org/doi/pdf/10.1021/acsomega.5c08189","citationCount":"0","resultStr":"{\"title\":\"Mechanism of Action and Anti-Inflammatory Activity of Pestalotioquinol A, a Fungus-Derived Cytoprotective Compound\",\"authors\":\"Yukine Tsurukawa, , , Yumi Katayama, , , Kazuki Kanno, , , Kanna Sato, , , Yuka Suzuki, , , Hironobu Murakami, , , Shiro Takeda, , , Motoharu Sakaue, , , Kazuyuki Sogawa, , , Yo Shinoda, , , Masaki Nagane, , , Naoyuki Aihara, , and , Shinji Kamisuki*, \",\"doi\":\"10.1021/acsomega.5c08189\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >Pestalotioquinol A (pesA) is a novel cytoprotective natural compound previously discovered among <i>Pestalotiopsis microspora</i> metabolites. PesA protects PC12 cells against cell death induced by a peroxynitrite donor, a reactive nitrogen species (RNS). In this study, we analyzed the mechanism of action of pesA and aimed to identify its target proteins. We revealed that the cytoprotective activity of pesA was specific to RNS, such as peroxynitrite and nitric oxide. A cellular thermal shift assay (CETSA) revealed elongation factor 1-α1 (EF1α1) as a potential pesA-binding protein. Cilostazol targeting EF1α1 displayed cytoprotective activity similar to pesA. EF1α1 knockdown increased peroxynitrite sensitivity and reduced the protective activity of pesA, suggesting that EF1α1 serves as a potential target. As RNSs are linked to inflammation, we examined the anti-inflammatory activity of pesA. PesA inhibited lipopolysaccharide-stimulated proinflammatory cytokine production in RAW264.7 cells. In an inflammatory bowel disease model mice, pesA significantly suppressed colon shortening and ameliorated total histopathological scores. PesA could help elucidate RNS-related events and serve as a lead compound for developing anti-inflammatory agents.</p>\",\"PeriodicalId\":22,\"journal\":{\"name\":\"ACS Omega\",\"volume\":\"10 41\",\"pages\":\"49243–49251\"},\"PeriodicalIF\":4.3000,\"publicationDate\":\"2025-10-08\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://pubs.acs.org/doi/pdf/10.1021/acsomega.5c08189\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"ACS Omega\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://pubs.acs.org/doi/10.1021/acsomega.5c08189\",\"RegionNum\":3,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Omega","FirstCategoryId":"92","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acsomega.5c08189","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
Mechanism of Action and Anti-Inflammatory Activity of Pestalotioquinol A, a Fungus-Derived Cytoprotective Compound
Pestalotioquinol A (pesA) is a novel cytoprotective natural compound previously discovered among Pestalotiopsis microspora metabolites. PesA protects PC12 cells against cell death induced by a peroxynitrite donor, a reactive nitrogen species (RNS). In this study, we analyzed the mechanism of action of pesA and aimed to identify its target proteins. We revealed that the cytoprotective activity of pesA was specific to RNS, such as peroxynitrite and nitric oxide. A cellular thermal shift assay (CETSA) revealed elongation factor 1-α1 (EF1α1) as a potential pesA-binding protein. Cilostazol targeting EF1α1 displayed cytoprotective activity similar to pesA. EF1α1 knockdown increased peroxynitrite sensitivity and reduced the protective activity of pesA, suggesting that EF1α1 serves as a potential target. As RNSs are linked to inflammation, we examined the anti-inflammatory activity of pesA. PesA inhibited lipopolysaccharide-stimulated proinflammatory cytokine production in RAW264.7 cells. In an inflammatory bowel disease model mice, pesA significantly suppressed colon shortening and ameliorated total histopathological scores. PesA could help elucidate RNS-related events and serve as a lead compound for developing anti-inflammatory agents.
ACS OmegaChemical Engineering-General Chemical Engineering
CiteScore
6.60
自引率
4.90%
发文量
3945
审稿时长
2.4 months
期刊介绍:
ACS Omega is an open-access global publication for scientific articles that describe new findings in chemistry and interfacing areas of science, without any perceived evaluation of immediate impact.