Haribaskar Ramachandran , Saskia Räuber , Jochen Dobner , Barbara Hildebrandt , Denise Haslinger , Andreas G. Chiocchetti , Paul Disse , Lara-Maria Preuth , Rajeevan Narayanan Therpurakal , Sven G. Meuth , Nico Melzer , Andrea Rossi
{"title":"将患者源性尿细胞重编程为iPSCs用于抗gad65自身免疫性脑炎研究。","authors":"Haribaskar Ramachandran , Saskia Räuber , Jochen Dobner , Barbara Hildebrandt , Denise Haslinger , Andreas G. Chiocchetti , Paul Disse , Lara-Maria Preuth , Rajeevan Narayanan Therpurakal , Sven G. Meuth , Nico Melzer , Andrea Rossi","doi":"10.1016/j.scr.2025.103790","DOIUrl":null,"url":null,"abstract":"<div><div>Urine cells from a patient with anti-GAD65<!--> <!-->autoantibody-associated autoimmune limbic encephalitis (ALE) were reprogrammed into<!--> <!-->iPSC<!--> <!-->line IUFi020-A. Pluripotency was confirmed through<!--> <!-->hiPSCore analysis while G-banding and CNV<!--> <!-->analysis demonstrated that IUFi020-A exhibits characteristic features of a bona fide iPSC line with no genetic changes compared to the donor urine cells. STR<!--> <!-->analysis further confirmed that IUFi020-A was derived from the parental urine cells. Additional characterization verified the absence of plasmid<!--> <!-->integration and mycoplasma contamination.<!--> <!-->IUFi020-A<!--> <!-->line provides a non-invasive alternative to fibroblast-based reprogramming and serves as a valuable model for investigating the pathogenic mechanisms of anti-GAD65-associated ALE.</div></div>","PeriodicalId":21843,"journal":{"name":"Stem cell research","volume":"87 ","pages":"Article 103790"},"PeriodicalIF":0.7000,"publicationDate":"2025-07-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Reprogramming Patient-Derived urine cells into iPSCs for Anti-GAD65 autoimmune encephalitis research\",\"authors\":\"Haribaskar Ramachandran , Saskia Räuber , Jochen Dobner , Barbara Hildebrandt , Denise Haslinger , Andreas G. Chiocchetti , Paul Disse , Lara-Maria Preuth , Rajeevan Narayanan Therpurakal , Sven G. Meuth , Nico Melzer , Andrea Rossi\",\"doi\":\"10.1016/j.scr.2025.103790\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Urine cells from a patient with anti-GAD65<!--> <!-->autoantibody-associated autoimmune limbic encephalitis (ALE) were reprogrammed into<!--> <!-->iPSC<!--> <!-->line IUFi020-A. Pluripotency was confirmed through<!--> <!-->hiPSCore analysis while G-banding and CNV<!--> <!-->analysis demonstrated that IUFi020-A exhibits characteristic features of a bona fide iPSC line with no genetic changes compared to the donor urine cells. STR<!--> <!-->analysis further confirmed that IUFi020-A was derived from the parental urine cells. Additional characterization verified the absence of plasmid<!--> <!-->integration and mycoplasma contamination.<!--> <!-->IUFi020-A<!--> <!-->line provides a non-invasive alternative to fibroblast-based reprogramming and serves as a valuable model for investigating the pathogenic mechanisms of anti-GAD65-associated ALE.</div></div>\",\"PeriodicalId\":21843,\"journal\":{\"name\":\"Stem cell research\",\"volume\":\"87 \",\"pages\":\"Article 103790\"},\"PeriodicalIF\":0.7000,\"publicationDate\":\"2025-07-28\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Stem cell research\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S1873506125001400\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"BIOTECHNOLOGY & APPLIED MICROBIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Stem cell research","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1873506125001400","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"BIOTECHNOLOGY & APPLIED MICROBIOLOGY","Score":null,"Total":0}
Reprogramming Patient-Derived urine cells into iPSCs for Anti-GAD65 autoimmune encephalitis research
Urine cells from a patient with anti-GAD65 autoantibody-associated autoimmune limbic encephalitis (ALE) were reprogrammed into iPSC line IUFi020-A. Pluripotency was confirmed through hiPSCore analysis while G-banding and CNV analysis demonstrated that IUFi020-A exhibits characteristic features of a bona fide iPSC line with no genetic changes compared to the donor urine cells. STR analysis further confirmed that IUFi020-A was derived from the parental urine cells. Additional characterization verified the absence of plasmid integration and mycoplasma contamination. IUFi020-A line provides a non-invasive alternative to fibroblast-based reprogramming and serves as a valuable model for investigating the pathogenic mechanisms of anti-GAD65-associated ALE.
期刊介绍:
Stem Cell Research is dedicated to publishing high-quality manuscripts focusing on the biology and applications of stem cell research. Submissions to Stem Cell Research, may cover all aspects of stem cells, including embryonic stem cells, tissue-specific stem cells, cancer stem cells, developmental studies, stem cell genomes, and translational research. Stem Cell Research publishes 6 issues a year.