J. Monk, Amber L. Hutchinson, Jamie L. A. Martin, L. Robinson
{"title":"利用免疫细胞/脂肪细胞共培养模型鉴定炎症旁分泌信号机制:长链N-3多不饱和脂肪酸减弱的过程","authors":"J. Monk, Amber L. Hutchinson, Jamie L. A. Martin, L. Robinson","doi":"10.33696/immunology.3.114","DOIUrl":null,"url":null,"abstract":"This invited Commentary is on the methods paper entitled “Studying adipocyte and immune cell cross talk using a co-culture system” in Immunometabolism: Methods and Protocols [1]. Co-culturing individual immune cell populations (as primary cells or cell lines) with adipocytes represents a model system to study the paracrine interactions (or cross-talk) between cell types that can impact adipose tissue (AT) function. This is particularly relevant in obese AT, wherein paracrine interactions between cell types promotes the secretion of inflammatory mediators that contribute to increased local (i.e. within the AT) and systemic low-grade inflammation and metabolic dysfunction, including insulin resistance (IR) [2-5].","PeriodicalId":73644,"journal":{"name":"Journal of cellular immunology","volume":" ","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2021-12-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Using Immune Cell/Adipocyte Co-Culture Models to Identify Inflammatory Paracrine Signaling Mechanisms: A Process Attenuated by Long-Chain N-3 Polyunsaturated Fatty Acids\",\"authors\":\"J. Monk, Amber L. Hutchinson, Jamie L. A. Martin, L. Robinson\",\"doi\":\"10.33696/immunology.3.114\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"This invited Commentary is on the methods paper entitled “Studying adipocyte and immune cell cross talk using a co-culture system” in Immunometabolism: Methods and Protocols [1]. Co-culturing individual immune cell populations (as primary cells or cell lines) with adipocytes represents a model system to study the paracrine interactions (or cross-talk) between cell types that can impact adipose tissue (AT) function. This is particularly relevant in obese AT, wherein paracrine interactions between cell types promotes the secretion of inflammatory mediators that contribute to increased local (i.e. within the AT) and systemic low-grade inflammation and metabolic dysfunction, including insulin resistance (IR) [2-5].\",\"PeriodicalId\":73644,\"journal\":{\"name\":\"Journal of cellular immunology\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2021-12-31\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of cellular immunology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.33696/immunology.3.114\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of cellular immunology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.33696/immunology.3.114","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Using Immune Cell/Adipocyte Co-Culture Models to Identify Inflammatory Paracrine Signaling Mechanisms: A Process Attenuated by Long-Chain N-3 Polyunsaturated Fatty Acids
This invited Commentary is on the methods paper entitled “Studying adipocyte and immune cell cross talk using a co-culture system” in Immunometabolism: Methods and Protocols [1]. Co-culturing individual immune cell populations (as primary cells or cell lines) with adipocytes represents a model system to study the paracrine interactions (or cross-talk) between cell types that can impact adipose tissue (AT) function. This is particularly relevant in obese AT, wherein paracrine interactions between cell types promotes the secretion of inflammatory mediators that contribute to increased local (i.e. within the AT) and systemic low-grade inflammation and metabolic dysfunction, including insulin resistance (IR) [2-5].