Benjamin J. Tajer , Glory Kalu , Sarah Jay , Eric Wynn , Antoine Decaux , Paul Gilbert , Hani D. Singer , Maddeline D. Kidd , Jeffery A. Nelson , Noora Harake , Noah J. Lopez , Nathan R. Souchet , Anna G. Luong , Aaron M. Savage , Sangwon Min , Alparslan Karabacak , Sebastian Böhm , Ryan T. Kim , Tim Froitzheim , Konstantinos Sousounis , Jessica L. Whited
{"title":"永生化蝾螈成纤维细胞的优化工具箱。","authors":"Benjamin J. Tajer , Glory Kalu , Sarah Jay , Eric Wynn , Antoine Decaux , Paul Gilbert , Hani D. Singer , Maddeline D. Kidd , Jeffery A. Nelson , Noora Harake , Noah J. Lopez , Nathan R. Souchet , Anna G. Luong , Aaron M. Savage , Sangwon Min , Alparslan Karabacak , Sebastian Böhm , Ryan T. Kim , Tim Froitzheim , Konstantinos Sousounis , Jessica L. Whited","doi":"10.1016/j.ymeth.2025.03.019","DOIUrl":null,"url":null,"abstract":"<div><div>The axolotl salamander model has broad utility for regeneration studies, but this model is limited by a lack of efficient cell-culture-based tools. The Axolotl Limb-1 (AL-1) fibroblast line, the only available immortalized axolotl cell line, was first published over 20 years ago, but many established molecular biology techniques, such as lipofectamine transfection, CRISPR-Cas9 mutagenesis, and antibiotic selection, work poorly or remain untested in AL-1 cells. Innovating technologies to manipulate AL-1 cells in culture and study their behavior following transplantation into the axolotl will complement <em>in-vivo</em> studies, decrease the number of animals used, and enable the faster, more streamlined investigation of regenerative biology questions. Here, we establish transfection, mutagenesis, antibiotic selection, and <em>in-vivo</em> transplantation techniques in axolotl AL-1 cells. These techniques will enable efficient culture with AL-1 cells and guide future tool development for the culture and manipulation of other salamander cell lines.</div></div>","PeriodicalId":390,"journal":{"name":"Methods","volume":"240 ","pages":"Pages 21-34"},"PeriodicalIF":4.2000,"publicationDate":"2025-04-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Optimized toolkit for the manipulation of immortalized axolotl fibroblasts\",\"authors\":\"Benjamin J. Tajer , Glory Kalu , Sarah Jay , Eric Wynn , Antoine Decaux , Paul Gilbert , Hani D. Singer , Maddeline D. Kidd , Jeffery A. Nelson , Noora Harake , Noah J. Lopez , Nathan R. Souchet , Anna G. Luong , Aaron M. Savage , Sangwon Min , Alparslan Karabacak , Sebastian Böhm , Ryan T. Kim , Tim Froitzheim , Konstantinos Sousounis , Jessica L. Whited\",\"doi\":\"10.1016/j.ymeth.2025.03.019\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>The axolotl salamander model has broad utility for regeneration studies, but this model is limited by a lack of efficient cell-culture-based tools. The Axolotl Limb-1 (AL-1) fibroblast line, the only available immortalized axolotl cell line, was first published over 20 years ago, but many established molecular biology techniques, such as lipofectamine transfection, CRISPR-Cas9 mutagenesis, and antibiotic selection, work poorly or remain untested in AL-1 cells. Innovating technologies to manipulate AL-1 cells in culture and study their behavior following transplantation into the axolotl will complement <em>in-vivo</em> studies, decrease the number of animals used, and enable the faster, more streamlined investigation of regenerative biology questions. Here, we establish transfection, mutagenesis, antibiotic selection, and <em>in-vivo</em> transplantation techniques in axolotl AL-1 cells. These techniques will enable efficient culture with AL-1 cells and guide future tool development for the culture and manipulation of other salamander cell lines.</div></div>\",\"PeriodicalId\":390,\"journal\":{\"name\":\"Methods\",\"volume\":\"240 \",\"pages\":\"Pages 21-34\"},\"PeriodicalIF\":4.2000,\"publicationDate\":\"2025-04-03\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Methods\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S1046202325000854\",\"RegionNum\":3,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"BIOCHEMICAL RESEARCH METHODS\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Methods","FirstCategoryId":"99","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1046202325000854","RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"BIOCHEMICAL RESEARCH METHODS","Score":null,"Total":0}
Optimized toolkit for the manipulation of immortalized axolotl fibroblasts
The axolotl salamander model has broad utility for regeneration studies, but this model is limited by a lack of efficient cell-culture-based tools. The Axolotl Limb-1 (AL-1) fibroblast line, the only available immortalized axolotl cell line, was first published over 20 years ago, but many established molecular biology techniques, such as lipofectamine transfection, CRISPR-Cas9 mutagenesis, and antibiotic selection, work poorly or remain untested in AL-1 cells. Innovating technologies to manipulate AL-1 cells in culture and study their behavior following transplantation into the axolotl will complement in-vivo studies, decrease the number of animals used, and enable the faster, more streamlined investigation of regenerative biology questions. Here, we establish transfection, mutagenesis, antibiotic selection, and in-vivo transplantation techniques in axolotl AL-1 cells. These techniques will enable efficient culture with AL-1 cells and guide future tool development for the culture and manipulation of other salamander cell lines.
期刊介绍:
Methods focuses on rapidly developing techniques in the experimental biological and medical sciences.
Each topical issue, organized by a guest editor who is an expert in the area covered, consists solely of invited quality articles by specialist authors, many of them reviews. Issues are devoted to specific technical approaches with emphasis on clear detailed descriptions of protocols that allow them to be reproduced easily. The background information provided enables researchers to understand the principles underlying the methods; other helpful sections include comparisons of alternative methods giving the advantages and disadvantages of particular methods, guidance on avoiding potential pitfalls, and suggestions for troubleshooting.