Jocelyn Cervantes, Anika Consul, Alan Tran, Jingjing Tang, Farah Kramer, Huaqing Zheng, Adam E Mullick, Tomas Vaisar, Francis Kim, Karin E Bornfeldt, Baohai Shao, Jenny E Kanter
{"title":"Hyperglycemia Drives an Activated, Lipid-Laden Nonclassical Monocyte Phenotype in Diabetes.","authors":"Jocelyn Cervantes, Anika Consul, Alan Tran, Jingjing Tang, Farah Kramer, Huaqing Zheng, Adam E Mullick, Tomas Vaisar, Francis Kim, Karin E Bornfeldt, Baohai Shao, Jenny E Kanter","doi":"10.2337/db26-0085","DOIUrl":null,"url":null,"abstract":"<p><strong>Article highlights: </strong>Although monocytes can accumulate lipids, whether diabetes alters monocyte lipid loading is unknown. Nonclassical monocytes accumulate more lipids via a process that is partly regulated by hyperglycemia in people with diabetes and in three different mouse models of diabetes. Increased lipid loading promotes a more activated monocyte phenotype. Nonclassical monocytes contribute to the accumulation of foamy kidney macrophages in a mouse model of diabetic kidney disease.</p>","PeriodicalId":93977,"journal":{"name":"Diabetes","volume":" ","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2026-10-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Diabetes","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.2337/db26-0085","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Article highlights: Although monocytes can accumulate lipids, whether diabetes alters monocyte lipid loading is unknown. Nonclassical monocytes accumulate more lipids via a process that is partly regulated by hyperglycemia in people with diabetes and in three different mouse models of diabetes. Increased lipid loading promotes a more activated monocyte phenotype. Nonclassical monocytes contribute to the accumulation of foamy kidney macrophages in a mouse model of diabetic kidney disease.