{"title":"半胱氨酸白三烯及其受体在免疫细胞相关功能中的作用。","authors":"Yoshihide Kanaoka, K Frank Austen","doi":"10.1016/bs.ai.2019.04.002","DOIUrl":null,"url":null,"abstract":"<p><p>The cysteinyl leukotrienes (cys-LTs), leukotriene C<sub>4</sub>, (LTC<sub>4</sub>), LTD<sub>4</sub>, and LTE<sub>4</sub>, are lipid mediators of inflammation. LTC<sub>4</sub> is the only intracellularly synthesized cys-LT through the 5-lipoxygenase and LTC<sub>4</sub> synthase pathway and after transport is metabolized to LTD<sub>4</sub> and LTE<sub>4</sub> by specific extracellular peptidases. Each cys-LT has a preferred functional receptor in vivo; LTD<sub>4</sub> to the type 1 cys-LT receptor (CysLT<sub>1</sub>R), LTC<sub>4</sub> to CysLT<sub>2</sub>R, and LTE<sub>4</sub> to CysLT<sub>3</sub>R (OXGR1 or GPR99). Recent studies in mouse models revealed that there are multiple regulatory mechanisms for these receptor functions and each receptor plays a distinct role as observed in different mouse models of inflammation and immune responses. This review focuses on the integrated host responses to the cys-LT/CysLTR pathway composed of sequential ligands with preferred receptors as seen from mouse models. It also discusses potential therapeutic targets for LTC<sub>4</sub> synthase, CysLT<sub>2</sub>R, and CysLT<sub>3</sub>R.</p>","PeriodicalId":50862,"journal":{"name":"Advances in Immunology","volume":"142 ","pages":"65-84"},"PeriodicalIF":0.0000,"publicationDate":"2019-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/bs.ai.2019.04.002","citationCount":"28","resultStr":"{\"title\":\"Roles of cysteinyl leukotrienes and their receptors in immune cell-related functions.\",\"authors\":\"Yoshihide Kanaoka, K Frank Austen\",\"doi\":\"10.1016/bs.ai.2019.04.002\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>The cysteinyl leukotrienes (cys-LTs), leukotriene C<sub>4</sub>, (LTC<sub>4</sub>), LTD<sub>4</sub>, and LTE<sub>4</sub>, are lipid mediators of inflammation. LTC<sub>4</sub> is the only intracellularly synthesized cys-LT through the 5-lipoxygenase and LTC<sub>4</sub> synthase pathway and after transport is metabolized to LTD<sub>4</sub> and LTE<sub>4</sub> by specific extracellular peptidases. Each cys-LT has a preferred functional receptor in vivo; LTD<sub>4</sub> to the type 1 cys-LT receptor (CysLT<sub>1</sub>R), LTC<sub>4</sub> to CysLT<sub>2</sub>R, and LTE<sub>4</sub> to CysLT<sub>3</sub>R (OXGR1 or GPR99). Recent studies in mouse models revealed that there are multiple regulatory mechanisms for these receptor functions and each receptor plays a distinct role as observed in different mouse models of inflammation and immune responses. This review focuses on the integrated host responses to the cys-LT/CysLTR pathway composed of sequential ligands with preferred receptors as seen from mouse models. It also discusses potential therapeutic targets for LTC<sub>4</sub> synthase, CysLT<sub>2</sub>R, and CysLT<sub>3</sub>R.</p>\",\"PeriodicalId\":50862,\"journal\":{\"name\":\"Advances in Immunology\",\"volume\":\"142 \",\"pages\":\"65-84\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2019-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1016/bs.ai.2019.04.002\",\"citationCount\":\"28\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Advances in Immunology\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1016/bs.ai.2019.04.002\",\"RegionNum\":3,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2019/5/14 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q2\",\"JCRName\":\"Medicine\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Advances in Immunology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1016/bs.ai.2019.04.002","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2019/5/14 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"Medicine","Score":null,"Total":0}
Roles of cysteinyl leukotrienes and their receptors in immune cell-related functions.
The cysteinyl leukotrienes (cys-LTs), leukotriene C4, (LTC4), LTD4, and LTE4, are lipid mediators of inflammation. LTC4 is the only intracellularly synthesized cys-LT through the 5-lipoxygenase and LTC4 synthase pathway and after transport is metabolized to LTD4 and LTE4 by specific extracellular peptidases. Each cys-LT has a preferred functional receptor in vivo; LTD4 to the type 1 cys-LT receptor (CysLT1R), LTC4 to CysLT2R, and LTE4 to CysLT3R (OXGR1 or GPR99). Recent studies in mouse models revealed that there are multiple regulatory mechanisms for these receptor functions and each receptor plays a distinct role as observed in different mouse models of inflammation and immune responses. This review focuses on the integrated host responses to the cys-LT/CysLTR pathway composed of sequential ligands with preferred receptors as seen from mouse models. It also discusses potential therapeutic targets for LTC4 synthase, CysLT2R, and CysLT3R.
期刊介绍:
Advances in Immunology has provided students and researchers with the latest information in Immunology for over 50 years. You can continue to rely on Advances in Immunology to provide you with critical reviews that examine subjects of vital importance to the field through summary and evaluation of current knowledge and research. The articles stress fundamental concepts, but also evaluate the experimental approaches.