Caffeic acid attenuates tissue damage and inflammatory response in Klebsiella pneumonia by modulating AhR‐Src‐STAT3‐IL‐10 signaling pathway
CA is a plant derivative with antibacterial and antiviral pharmacological effects, however, the therapeutic effect of CA on Klebsiella pneumonia and its mechanism study is still unclear. A rat KP model was established in vitro, a pneumonia cell model was established in vivo, the histopathological ch...
Gespeichert in:
Veröffentlicht in: | Environmental toxicology 2024-04, Vol.39 (4), p.2254-2264 |
---|---|
Hauptverfasser: | , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 2264 |
---|---|
container_issue | 4 |
container_start_page | 2254 |
container_title | Environmental toxicology |
container_volume | 39 |
creator | Chen, Mei‐ling Jiang, Hui‐yu Zeng, Jun Huang, Ling Lv, Chuan‐zhu |
description | CA is a plant derivative with antibacterial and antiviral pharmacological effects, however, the therapeutic effect of CA on Klebsiella pneumonia and its mechanism study is still unclear. A rat KP model was established in vitro, a pneumonia cell model was established in vivo, the histopathological changes in the lungs were observed by HE staining after CA treatment, the expression of relevant inflammatory factors was detected by ELISA, the changes in the expression of proteins related to the AhR‐Src‐STAT3‐IL‐10 signaling pathway were detected by Western blot and immunofluorescence in the lungs, and the interactions between the proteins were verified by COIP relationship. The results showed that CA was able to attenuate the injury and inflammatory response of lung tissues, and molecular docking showed that there were binding sites between CA and AhR, and COIP demonstrated that AhR interacted with both STAT3 and Ser. In addition, CA was able to up‐regulate the expression levels of pathway‐related proteins of AhR, IL‐10, p‐Src, and p‐STAT3, and AhR knockdown was able to reduce LPS‐induced inflammatory responses and up‐regulate pathway‐related proteins, whereas CA treatment of AhR‐knockdown‐treated A549 cells did not show any statistically significant difference compared with the AhR knockdown group, demonstrating that CA exerts its pharmacological effects. These findings elucidated the mechanism of CA in the treatment of KP and demonstrated that CA is a potential therapeutic agent for KP. |
doi_str_mv | 10.1002/tox.24086 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2906772992</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2942087517</sourcerecordid><originalsourceid>FETCH-LOGICAL-c3136-d3a7ce591c085afb7f726b0232f4b9506c9eb859111dcb8c14c9dfdc3c5fe0e63</originalsourceid><addsrcrecordid>eNp1kc2K1UAQhRtRnHF04QtIgxtdZKZ_ku5kebn4M3hhQK_gLlQ61Xd6SNKxO2HMzkcQfEOfxM7c0YXgpqo49XGo4hDynLNzzpi4mPy3c5GzUj0gp7wQItNClw_vZpYlnZ-QJzHeMMYqVajH5ESWPC-VVKfk5xasRWcoGNdSmCYcZpgw0snFOCNtoYcDUhha6gbbQd_D5MNCA8bRDxGTSj902ESHXQd0HHDu_eCANgvtfTt3MLnhQDfXH399__EpmLXuN3uZ-uUuFc5odIcBupUaYbq-heUpeWShi_jsvp-Rz2_f7Lfvs93Vu8vtZpcZyaXKWgnaYFFxw8oCbKOtFqphQgqbN1XBlKmwKdOe89Y0peG5qVrbGmkKiwyVPCOvjr5j8F9njFPdu2jWPwb0c6xFxZTWoqpEQl_-g974OaSzVyoXrNQF14l6faRM8DEGtPUYXA9hqTmr16TqlFR9l1RiX9w7zk2P7V_yTzQJuDgCt67D5f9O9f7qy9HyN41YotQ</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2942087517</pqid></control><display><type>article</type><title>Caffeic acid attenuates tissue damage and inflammatory response in Klebsiella pneumonia by modulating AhR‐Src‐STAT3‐IL‐10 signaling pathway</title><source>MEDLINE</source><source>Wiley Journals</source><creator>Chen, Mei‐ling ; Jiang, Hui‐yu ; Zeng, Jun ; Huang, Ling ; Lv, Chuan‐zhu</creator><creatorcontrib>Chen, Mei‐ling ; Jiang, Hui‐yu ; Zeng, Jun ; Huang, Ling ; Lv, Chuan‐zhu</creatorcontrib><description>CA is a plant derivative with antibacterial and antiviral pharmacological effects, however, the therapeutic effect of CA on Klebsiella pneumonia and its mechanism study is still unclear. A rat KP model was established in vitro, a pneumonia cell model was established in vivo, the histopathological changes in the lungs were observed by HE staining after CA treatment, the expression of relevant inflammatory factors was detected by ELISA, the changes in the expression of proteins related to the AhR‐Src‐STAT3‐IL‐10 signaling pathway were detected by Western blot and immunofluorescence in the lungs, and the interactions between the proteins were verified by COIP relationship. The results showed that CA was able to attenuate the injury and inflammatory response of lung tissues, and molecular docking showed that there were binding sites between CA and AhR, and COIP demonstrated that AhR interacted with both STAT3 and Ser. In addition, CA was able to up‐regulate the expression levels of pathway‐related proteins of AhR, IL‐10, p‐Src, and p‐STAT3, and AhR knockdown was able to reduce LPS‐induced inflammatory responses and up‐regulate pathway‐related proteins, whereas CA treatment of AhR‐knockdown‐treated A549 cells did not show any statistically significant difference compared with the AhR knockdown group, demonstrating that CA exerts its pharmacological effects. These findings elucidated the mechanism of CA in the treatment of KP and demonstrated that CA is a potential therapeutic agent for KP.</description><identifier>ISSN: 1520-4081</identifier><identifier>EISSN: 1522-7278</identifier><identifier>DOI: 10.1002/tox.24086</identifier><identifier>PMID: 38148636</identifier><language>eng</language><publisher>Hoboken, USA: John Wiley & Sons, Inc</publisher><subject>Animals ; Antibiotics ; Antiviral agents ; aryl hydrocarbon receptor ; Binding sites ; Caffeic acid ; Caffeic Acids ; ELISA ; Enzyme-linked immunosorbent assay ; Histopathology ; IL‐10 ; Immunofluorescence ; Inflammation ; Inflammatory response ; Interleukin-10 ; Klebsiella ; Klebsiella - metabolism ; Klebsiella pneumonia ; Klebsiella pneumoniae ; Lungs ; Molecular docking ; Molecular Docking Simulation ; Pharmacology ; Pneumonia ; Pneumonia - drug therapy ; Proteins ; Rats ; Receptors, Aryl Hydrocarbon - genetics ; Receptors, Aryl Hydrocarbon - metabolism ; Signal Transduction ; Src ; STAT3 ; Stat3 protein ; Statistical analysis</subject><ispartof>Environmental toxicology, 2024-04, Vol.39 (4), p.2254-2264</ispartof><rights>2023 Wiley Periodicals LLC.</rights><rights>2024 Wiley Periodicals LLC.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c3136-d3a7ce591c085afb7f726b0232f4b9506c9eb859111dcb8c14c9dfdc3c5fe0e63</cites><orcidid>0009-0004-4309-0007</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Ftox.24086$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Ftox.24086$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38148636$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Chen, Mei‐ling</creatorcontrib><creatorcontrib>Jiang, Hui‐yu</creatorcontrib><creatorcontrib>Zeng, Jun</creatorcontrib><creatorcontrib>Huang, Ling</creatorcontrib><creatorcontrib>Lv, Chuan‐zhu</creatorcontrib><title>Caffeic acid attenuates tissue damage and inflammatory response in Klebsiella pneumonia by modulating AhR‐Src‐STAT3‐IL‐10 signaling pathway</title><title>Environmental toxicology</title><addtitle>Environ Toxicol</addtitle><description>CA is a plant derivative with antibacterial and antiviral pharmacological effects, however, the therapeutic effect of CA on Klebsiella pneumonia and its mechanism study is still unclear. A rat KP model was established in vitro, a pneumonia cell model was established in vivo, the histopathological changes in the lungs were observed by HE staining after CA treatment, the expression of relevant inflammatory factors was detected by ELISA, the changes in the expression of proteins related to the AhR‐Src‐STAT3‐IL‐10 signaling pathway were detected by Western blot and immunofluorescence in the lungs, and the interactions between the proteins were verified by COIP relationship. The results showed that CA was able to attenuate the injury and inflammatory response of lung tissues, and molecular docking showed that there were binding sites between CA and AhR, and COIP demonstrated that AhR interacted with both STAT3 and Ser. In addition, CA was able to up‐regulate the expression levels of pathway‐related proteins of AhR, IL‐10, p‐Src, and p‐STAT3, and AhR knockdown was able to reduce LPS‐induced inflammatory responses and up‐regulate pathway‐related proteins, whereas CA treatment of AhR‐knockdown‐treated A549 cells did not show any statistically significant difference compared with the AhR knockdown group, demonstrating that CA exerts its pharmacological effects. These findings elucidated the mechanism of CA in the treatment of KP and demonstrated that CA is a potential therapeutic agent for KP.</description><subject>Animals</subject><subject>Antibiotics</subject><subject>Antiviral agents</subject><subject>aryl hydrocarbon receptor</subject><subject>Binding sites</subject><subject>Caffeic acid</subject><subject>Caffeic Acids</subject><subject>ELISA</subject><subject>Enzyme-linked immunosorbent assay</subject><subject>Histopathology</subject><subject>IL‐10</subject><subject>Immunofluorescence</subject><subject>Inflammation</subject><subject>Inflammatory response</subject><subject>Interleukin-10</subject><subject>Klebsiella</subject><subject>Klebsiella - metabolism</subject><subject>Klebsiella pneumonia</subject><subject>Klebsiella pneumoniae</subject><subject>Lungs</subject><subject>Molecular docking</subject><subject>Molecular Docking Simulation</subject><subject>Pharmacology</subject><subject>Pneumonia</subject><subject>Pneumonia - drug therapy</subject><subject>Proteins</subject><subject>Rats</subject><subject>Receptors, Aryl Hydrocarbon - genetics</subject><subject>Receptors, Aryl Hydrocarbon - metabolism</subject><subject>Signal Transduction</subject><subject>Src</subject><subject>STAT3</subject><subject>Stat3 protein</subject><subject>Statistical analysis</subject><issn>1520-4081</issn><issn>1522-7278</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kc2K1UAQhRtRnHF04QtIgxtdZKZ_ku5kebn4M3hhQK_gLlQ61Xd6SNKxO2HMzkcQfEOfxM7c0YXgpqo49XGo4hDynLNzzpi4mPy3c5GzUj0gp7wQItNClw_vZpYlnZ-QJzHeMMYqVajH5ESWPC-VVKfk5xasRWcoGNdSmCYcZpgw0snFOCNtoYcDUhha6gbbQd_D5MNCA8bRDxGTSj902ESHXQd0HHDu_eCANgvtfTt3MLnhQDfXH399__EpmLXuN3uZ-uUuFc5odIcBupUaYbq-heUpeWShi_jsvp-Rz2_f7Lfvs93Vu8vtZpcZyaXKWgnaYFFxw8oCbKOtFqphQgqbN1XBlKmwKdOe89Y0peG5qVrbGmkKiwyVPCOvjr5j8F9njFPdu2jWPwb0c6xFxZTWoqpEQl_-g974OaSzVyoXrNQF14l6faRM8DEGtPUYXA9hqTmr16TqlFR9l1RiX9w7zk2P7V_yTzQJuDgCt67D5f9O9f7qy9HyN41YotQ</recordid><startdate>202404</startdate><enddate>202404</enddate><creator>Chen, Mei‐ling</creator><creator>Jiang, Hui‐yu</creator><creator>Zeng, Jun</creator><creator>Huang, Ling</creator><creator>Lv, Chuan‐zhu</creator><general>John Wiley & Sons, Inc</general><general>Wiley Subscription Services, Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QH</scope><scope>7ST</scope><scope>7TN</scope><scope>7U7</scope><scope>7UA</scope><scope>C1K</scope><scope>F1W</scope><scope>H97</scope><scope>K9.</scope><scope>L.G</scope><scope>M7N</scope><scope>SOI</scope><scope>7X8</scope><orcidid>https://orcid.org/0009-0004-4309-0007</orcidid></search><sort><creationdate>202404</creationdate><title>Caffeic acid attenuates tissue damage and inflammatory response in Klebsiella pneumonia by modulating AhR‐Src‐STAT3‐IL‐10 signaling pathway</title><author>Chen, Mei‐ling ; Jiang, Hui‐yu ; Zeng, Jun ; Huang, Ling ; Lv, Chuan‐zhu</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3136-d3a7ce591c085afb7f726b0232f4b9506c9eb859111dcb8c14c9dfdc3c5fe0e63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Animals</topic><topic>Antibiotics</topic><topic>Antiviral agents</topic><topic>aryl hydrocarbon receptor</topic><topic>Binding sites</topic><topic>Caffeic acid</topic><topic>Caffeic Acids</topic><topic>ELISA</topic><topic>Enzyme-linked immunosorbent assay</topic><topic>Histopathology</topic><topic>IL‐10</topic><topic>Immunofluorescence</topic><topic>Inflammation</topic><topic>Inflammatory response</topic><topic>Interleukin-10</topic><topic>Klebsiella</topic><topic>Klebsiella - metabolism</topic><topic>Klebsiella pneumonia</topic><topic>Klebsiella pneumoniae</topic><topic>Lungs</topic><topic>Molecular docking</topic><topic>Molecular Docking Simulation</topic><topic>Pharmacology</topic><topic>Pneumonia</topic><topic>Pneumonia - drug therapy</topic><topic>Proteins</topic><topic>Rats</topic><topic>Receptors, Aryl Hydrocarbon - genetics</topic><topic>Receptors, Aryl Hydrocarbon - metabolism</topic><topic>Signal Transduction</topic><topic>Src</topic><topic>STAT3</topic><topic>Stat3 protein</topic><topic>Statistical analysis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chen, Mei‐ling</creatorcontrib><creatorcontrib>Jiang, Hui‐yu</creatorcontrib><creatorcontrib>Zeng, Jun</creatorcontrib><creatorcontrib>Huang, Ling</creatorcontrib><creatorcontrib>Lv, Chuan‐zhu</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Aqualine</collection><collection>Environment Abstracts</collection><collection>Oceanic Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Water Resources Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ASFA: Aquatic Sciences and Fisheries Abstracts</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) 3: Aquatic Pollution & Environmental Quality</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) Professional</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Environment Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Environmental toxicology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chen, Mei‐ling</au><au>Jiang, Hui‐yu</au><au>Zeng, Jun</au><au>Huang, Ling</au><au>Lv, Chuan‐zhu</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Caffeic acid attenuates tissue damage and inflammatory response in Klebsiella pneumonia by modulating AhR‐Src‐STAT3‐IL‐10 signaling pathway</atitle><jtitle>Environmental toxicology</jtitle><addtitle>Environ Toxicol</addtitle><date>2024-04</date><risdate>2024</risdate><volume>39</volume><issue>4</issue><spage>2254</spage><epage>2264</epage><pages>2254-2264</pages><issn>1520-4081</issn><eissn>1522-7278</eissn><abstract>CA is a plant derivative with antibacterial and antiviral pharmacological effects, however, the therapeutic effect of CA on Klebsiella pneumonia and its mechanism study is still unclear. A rat KP model was established in vitro, a pneumonia cell model was established in vivo, the histopathological changes in the lungs were observed by HE staining after CA treatment, the expression of relevant inflammatory factors was detected by ELISA, the changes in the expression of proteins related to the AhR‐Src‐STAT3‐IL‐10 signaling pathway were detected by Western blot and immunofluorescence in the lungs, and the interactions between the proteins were verified by COIP relationship. The results showed that CA was able to attenuate the injury and inflammatory response of lung tissues, and molecular docking showed that there were binding sites between CA and AhR, and COIP demonstrated that AhR interacted with both STAT3 and Ser. In addition, CA was able to up‐regulate the expression levels of pathway‐related proteins of AhR, IL‐10, p‐Src, and p‐STAT3, and AhR knockdown was able to reduce LPS‐induced inflammatory responses and up‐regulate pathway‐related proteins, whereas CA treatment of AhR‐knockdown‐treated A549 cells did not show any statistically significant difference compared with the AhR knockdown group, demonstrating that CA exerts its pharmacological effects. These findings elucidated the mechanism of CA in the treatment of KP and demonstrated that CA is a potential therapeutic agent for KP.</abstract><cop>Hoboken, USA</cop><pub>John Wiley & Sons, Inc</pub><pmid>38148636</pmid><doi>10.1002/tox.24086</doi><tpages>11</tpages><orcidid>https://orcid.org/0009-0004-4309-0007</orcidid></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1520-4081 |
ispartof | Environmental toxicology, 2024-04, Vol.39 (4), p.2254-2264 |
issn | 1520-4081 1522-7278 |
language | eng |
recordid | cdi_proquest_miscellaneous_2906772992 |
source | MEDLINE; Wiley Journals |
subjects | Animals Antibiotics Antiviral agents aryl hydrocarbon receptor Binding sites Caffeic acid Caffeic Acids ELISA Enzyme-linked immunosorbent assay Histopathology IL‐10 Immunofluorescence Inflammation Inflammatory response Interleukin-10 Klebsiella Klebsiella - metabolism Klebsiella pneumonia Klebsiella pneumoniae Lungs Molecular docking Molecular Docking Simulation Pharmacology Pneumonia Pneumonia - drug therapy Proteins Rats Receptors, Aryl Hydrocarbon - genetics Receptors, Aryl Hydrocarbon - metabolism Signal Transduction Src STAT3 Stat3 protein Statistical analysis |
title | Caffeic acid attenuates tissue damage and inflammatory response in Klebsiella pneumonia by modulating AhR‐Src‐STAT3‐IL‐10 signaling pathway |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-29T06%3A20%3A57IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Caffeic%20acid%20attenuates%20tissue%20damage%20and%20inflammatory%20response%20in%20Klebsiella%20pneumonia%20by%20modulating%20AhR%E2%80%90Src%E2%80%90STAT3%E2%80%90IL%E2%80%9010%20signaling%20pathway&rft.jtitle=Environmental%20toxicology&rft.au=Chen,%20Mei%E2%80%90ling&rft.date=2024-04&rft.volume=39&rft.issue=4&rft.spage=2254&rft.epage=2264&rft.pages=2254-2264&rft.issn=1520-4081&rft.eissn=1522-7278&rft_id=info:doi/10.1002/tox.24086&rft_dat=%3Cproquest_cross%3E2942087517%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2942087517&rft_id=info:pmid/38148636&rfr_iscdi=true |