{"title":"动力蛋白相关蛋白1通过与己糖激酶1的相互作用调控牙周巨噬细胞的炎症反应","authors":"Yiming Jiang, Zihan Wang, Kaige Zhang, Yue Hu, Dehao Shang, Lulu Jiang, Minghao Huang, Biyao Wang, Xiaomin He, Zhou Wu, Xu Yan, Xinwen Zhang","doi":"10.1111/jcpe.14111","DOIUrl":null,"url":null,"abstract":"AimTo explore the potential roles of mitochondrial dysfunction in the initiation of inflammation in periodontal macrophages and to determine the mechanism underlying the involvement of dynamin‐related protein 1 (Drp1) in macrophage inflammatory responses through its interaction with hexokinase 1 (HK1).Materials and MethodsGingival tissues were collected from patients diagnosed with periodontitis or from healthy volunteers. Drp1 tetramer formation and phosphorylation were analysed using western blot. THP‐1 macrophages and RAW264.7 cells were stimulated with <jats:styled-content style=\"fixed-case\"><jats:italic>Porphyromonas gingivalis</jats:italic></jats:styled-content> (<jats:italic>Pg</jats:italic>) or <jats:italic>Pg</jats:italic> lipopolysaccharide (<jats:italic>Pg</jats:italic> LPS), respectively. Alterations in proteins associated with mitochondrial dynamics were scrutinized via western blot. Immunofluorescence was used to evaluate mitochondrial damage and mitochondrial permeability transition pore (mPTP) opening. Western blot was used to examine the inflammatory markers NLRP3, caspase‐1, IL‐1β and GSDMD. Protein interactions involving Drp1 were verified through immunoprecipitation.ResultsIn periodontitis patient samples, <jats:italic>Pg</jats:italic> LPS‐treated RAW264.7 cells, and <jats:italic>Pg</jats:italic>‐stimulated THP‐1 macrophages, over‐activated Drp1 was able to drive NLRP3 inflammasome activation and the subsequent release of inflammatory factors. A direct interaction between Drp1 and HK1 was observed, facilitating excessive mPTP opening and subsequent mitochondrial dysfunction.ConclusionIn the inflammatory milieu of periodontal tissues, Drp1 hyperactivation in the macrophages is implicated in inflammation induction. Modulation of the inflammatory response in periodontal macrophages by Drp1 appears to facilitate mPTP opening.","PeriodicalId":15380,"journal":{"name":"Journal of Clinical Periodontology","volume":"5 1","pages":""},"PeriodicalIF":5.8000,"publicationDate":"2025-01-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Dynamin‐Related Protein 1 Orchestrates Inflammatory Responses in Periodontal Macrophages via Interaction With Hexokinase 1\",\"authors\":\"Yiming Jiang, Zihan Wang, Kaige Zhang, Yue Hu, Dehao Shang, Lulu Jiang, Minghao Huang, Biyao Wang, Xiaomin He, Zhou Wu, Xu Yan, Xinwen Zhang\",\"doi\":\"10.1111/jcpe.14111\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"AimTo explore the potential roles of mitochondrial dysfunction in the initiation of inflammation in periodontal macrophages and to determine the mechanism underlying the involvement of dynamin‐related protein 1 (Drp1) in macrophage inflammatory responses through its interaction with hexokinase 1 (HK1).Materials and MethodsGingival tissues were collected from patients diagnosed with periodontitis or from healthy volunteers. Drp1 tetramer formation and phosphorylation were analysed using western blot. THP‐1 macrophages and RAW264.7 cells were stimulated with <jats:styled-content style=\\\"fixed-case\\\"><jats:italic>Porphyromonas gingivalis</jats:italic></jats:styled-content> (<jats:italic>Pg</jats:italic>) or <jats:italic>Pg</jats:italic> lipopolysaccharide (<jats:italic>Pg</jats:italic> LPS), respectively. Alterations in proteins associated with mitochondrial dynamics were scrutinized via western blot. Immunofluorescence was used to evaluate mitochondrial damage and mitochondrial permeability transition pore (mPTP) opening. Western blot was used to examine the inflammatory markers NLRP3, caspase‐1, IL‐1β and GSDMD. Protein interactions involving Drp1 were verified through immunoprecipitation.ResultsIn periodontitis patient samples, <jats:italic>Pg</jats:italic> LPS‐treated RAW264.7 cells, and <jats:italic>Pg</jats:italic>‐stimulated THP‐1 macrophages, over‐activated Drp1 was able to drive NLRP3 inflammasome activation and the subsequent release of inflammatory factors. A direct interaction between Drp1 and HK1 was observed, facilitating excessive mPTP opening and subsequent mitochondrial dysfunction.ConclusionIn the inflammatory milieu of periodontal tissues, Drp1 hyperactivation in the macrophages is implicated in inflammation induction. Modulation of the inflammatory response in periodontal macrophages by Drp1 appears to facilitate mPTP opening.\",\"PeriodicalId\":15380,\"journal\":{\"name\":\"Journal of Clinical Periodontology\",\"volume\":\"5 1\",\"pages\":\"\"},\"PeriodicalIF\":5.8000,\"publicationDate\":\"2025-01-07\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Clinical Periodontology\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1111/jcpe.14111\",\"RegionNum\":1,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"DENTISTRY, ORAL SURGERY & MEDICINE\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Clinical Periodontology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1111/jcpe.14111","RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"DENTISTRY, ORAL SURGERY & MEDICINE","Score":null,"Total":0}
Dynamin‐Related Protein 1 Orchestrates Inflammatory Responses in Periodontal Macrophages via Interaction With Hexokinase 1
AimTo explore the potential roles of mitochondrial dysfunction in the initiation of inflammation in periodontal macrophages and to determine the mechanism underlying the involvement of dynamin‐related protein 1 (Drp1) in macrophage inflammatory responses through its interaction with hexokinase 1 (HK1).Materials and MethodsGingival tissues were collected from patients diagnosed with periodontitis or from healthy volunteers. Drp1 tetramer formation and phosphorylation were analysed using western blot. THP‐1 macrophages and RAW264.7 cells were stimulated with Porphyromonas gingivalis (Pg) or Pg lipopolysaccharide (Pg LPS), respectively. Alterations in proteins associated with mitochondrial dynamics were scrutinized via western blot. Immunofluorescence was used to evaluate mitochondrial damage and mitochondrial permeability transition pore (mPTP) opening. Western blot was used to examine the inflammatory markers NLRP3, caspase‐1, IL‐1β and GSDMD. Protein interactions involving Drp1 were verified through immunoprecipitation.ResultsIn periodontitis patient samples, Pg LPS‐treated RAW264.7 cells, and Pg‐stimulated THP‐1 macrophages, over‐activated Drp1 was able to drive NLRP3 inflammasome activation and the subsequent release of inflammatory factors. A direct interaction between Drp1 and HK1 was observed, facilitating excessive mPTP opening and subsequent mitochondrial dysfunction.ConclusionIn the inflammatory milieu of periodontal tissues, Drp1 hyperactivation in the macrophages is implicated in inflammation induction. Modulation of the inflammatory response in periodontal macrophages by Drp1 appears to facilitate mPTP opening.
期刊介绍:
Journal of Clinical Periodontology was founded by the British, Dutch, French, German, Scandinavian, and Swiss Societies of Periodontology.
The aim of the Journal of Clinical Periodontology is to provide the platform for exchange of scientific and clinical progress in the field of Periodontology and allied disciplines, and to do so at the highest possible level. The Journal also aims to facilitate the application of new scientific knowledge to the daily practice of the concerned disciplines and addresses both practicing clinicians and academics. The Journal is the official publication of the European Federation of Periodontology but wishes to retain its international scope.
The Journal publishes original contributions of high scientific merit in the fields of periodontology and implant dentistry. Its scope encompasses the physiology and pathology of the periodontium, the tissue integration of dental implants, the biology and the modulation of periodontal and alveolar bone healing and regeneration, diagnosis, epidemiology, prevention and therapy of periodontal disease, the clinical aspects of tooth replacement with dental implants, and the comprehensive rehabilitation of the periodontal patient. Review articles by experts on new developments in basic and applied periodontal science and associated dental disciplines, advances in periodontal or implant techniques and procedures, and case reports which illustrate important new information are also welcome.