Aoran Huang , Jianyun Rao , Xin Feng , Xingru Li , Tianhua Xu , Li Yao
{"title":"开辟新天地:揭示血管钙化中的 USP1/ID3/E12/P21 轴。","authors":"Aoran Huang , Jianyun Rao , Xin Feng , Xingru Li , Tianhua Xu , Li Yao","doi":"10.1016/j.trsl.2024.09.002","DOIUrl":null,"url":null,"abstract":"<div><div>Vascular calcification (VC) poses significant challenges in cardiovascular health. This study employs single-cell transcriptome sequencing to dissect cellular dynamics in this process. We identify distinct cell subgroups, notably in vascular smooth muscle cells (VSMCs), and observe differences between calcified atherosclerotic cores and adjacent regions. Further exploration reveals ID3 as a key gene regulating VSMC function. In vitro experiments demonstrate ID3′s interaction with USP1 and E12, modulating cell proliferation and osteogenic differentiation. Animal models confirm the critical role of the USP1/ID3/E12/P21 axis in VC. This study sheds light on a novel regulatory mechanism, offering potential therapeutic targets.<ul><li><span>1.</span><span><div>This study uses single-cell transcriptome to investigate vascular calcification in depth.</div></span></li><li><span>2.</span><span><div>This study successfully identifies cellular heterogeneity related to vascular calcification.</div></span></li><li><span>3.</span><span><div>This study reveals the crucial role of ID3 in vascular smooth muscle cell osteogenic differentiation.</div></span></li><li><span>4.</span><span><div><em>In vivo</em> and <em>in vitro</em> experiments of this study demonstrate the regulatory role of the USP1/ID3/E12/P21 axis in calcification.</div></span></li><li><span>5.</span><span><div>This study provides potential molecular targets for the treatment of calcification-related diseases.</div></span></li></ul></div></div>","PeriodicalId":23226,"journal":{"name":"Translational Research","volume":"276 ","pages":"Pages 1-20"},"PeriodicalIF":6.4000,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Breaking new ground: Unraveling the USP1/ID3/E12/P21 axis in vascular calcification\",\"authors\":\"Aoran Huang , Jianyun Rao , Xin Feng , Xingru Li , Tianhua Xu , Li Yao\",\"doi\":\"10.1016/j.trsl.2024.09.002\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Vascular calcification (VC) poses significant challenges in cardiovascular health. This study employs single-cell transcriptome sequencing to dissect cellular dynamics in this process. We identify distinct cell subgroups, notably in vascular smooth muscle cells (VSMCs), and observe differences between calcified atherosclerotic cores and adjacent regions. Further exploration reveals ID3 as a key gene regulating VSMC function. In vitro experiments demonstrate ID3′s interaction with USP1 and E12, modulating cell proliferation and osteogenic differentiation. Animal models confirm the critical role of the USP1/ID3/E12/P21 axis in VC. This study sheds light on a novel regulatory mechanism, offering potential therapeutic targets.<ul><li><span>1.</span><span><div>This study uses single-cell transcriptome to investigate vascular calcification in depth.</div></span></li><li><span>2.</span><span><div>This study successfully identifies cellular heterogeneity related to vascular calcification.</div></span></li><li><span>3.</span><span><div>This study reveals the crucial role of ID3 in vascular smooth muscle cell osteogenic differentiation.</div></span></li><li><span>4.</span><span><div><em>In vivo</em> and <em>in vitro</em> experiments of this study demonstrate the regulatory role of the USP1/ID3/E12/P21 axis in calcification.</div></span></li><li><span>5.</span><span><div>This study provides potential molecular targets for the treatment of calcification-related diseases.</div></span></li></ul></div></div>\",\"PeriodicalId\":23226,\"journal\":{\"name\":\"Translational Research\",\"volume\":\"276 \",\"pages\":\"Pages 1-20\"},\"PeriodicalIF\":6.4000,\"publicationDate\":\"2025-02-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Translational Research\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S1931524424001701\",\"RegionNum\":2,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"MEDICAL LABORATORY TECHNOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Translational Research","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1931524424001701","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"MEDICAL LABORATORY TECHNOLOGY","Score":null,"Total":0}
Breaking new ground: Unraveling the USP1/ID3/E12/P21 axis in vascular calcification
Vascular calcification (VC) poses significant challenges in cardiovascular health. This study employs single-cell transcriptome sequencing to dissect cellular dynamics in this process. We identify distinct cell subgroups, notably in vascular smooth muscle cells (VSMCs), and observe differences between calcified atherosclerotic cores and adjacent regions. Further exploration reveals ID3 as a key gene regulating VSMC function. In vitro experiments demonstrate ID3′s interaction with USP1 and E12, modulating cell proliferation and osteogenic differentiation. Animal models confirm the critical role of the USP1/ID3/E12/P21 axis in VC. This study sheds light on a novel regulatory mechanism, offering potential therapeutic targets.
1.
This study uses single-cell transcriptome to investigate vascular calcification in depth.
2.
This study successfully identifies cellular heterogeneity related to vascular calcification.
3.
This study reveals the crucial role of ID3 in vascular smooth muscle cell osteogenic differentiation.
4.
In vivo and in vitro experiments of this study demonstrate the regulatory role of the USP1/ID3/E12/P21 axis in calcification.
5.
This study provides potential molecular targets for the treatment of calcification-related diseases.
期刊介绍:
Translational Research (formerly The Journal of Laboratory and Clinical Medicine) delivers original investigations in the broad fields of laboratory, clinical, and public health research. Published monthly since 1915, it keeps readers up-to-date on significant biomedical research from all subspecialties of medicine.