Madhusudhanan Sukumar, Jie Liu, Gautam U Mehta, Shashank J Patel, Rahul Roychoudhuri, Joseph G Crompton, Christopher A Klebanoff, Yun Ji, Peng Li, Zhiya Yu, Greg D Whitehill, David Clever, Robert L Eil, Douglas C Palmer, Suman Mitra, Mahadev Rao, Keyvan Keyvanfar, David S Schrump, Ena Wang, Francesco M Marincola, Luca Gattinoni, Warren J Leonard, Pawel Muranski, Toren Finkel, Nicholas P Restifo
{"title":"Mitochondrial Membrane Potential Identifies Cells with Enhanced Stemness for Cellular Therapy.","authors":"Madhusudhanan Sukumar, Jie Liu, Gautam U Mehta, Shashank J Patel, Rahul Roychoudhuri, Joseph G Crompton, Christopher A Klebanoff, Yun Ji, Peng Li, Zhiya Yu, Greg D Whitehill, David Clever, Robert L Eil, Douglas C Palmer, Suman Mitra, Mahadev Rao, Keyvan Keyvanfar, David S Schrump, Ena Wang, Francesco M Marincola, Luca Gattinoni, Warren J Leonard, Pawel Muranski, Toren Finkel, Nicholas P Restifo","doi":"10.1016/j.cmet.2015.11.002","DOIUrl":null,"url":null,"abstract":"<p><p>Long-term survival and antitumor immunity of adoptively transferred CD8(+) T cells is dependent on their metabolic fitness, but approaches to isolate therapeutic T cells based on metabolic features are not well established. Here we utilized a lipophilic cationic dye tetramethylrhodamine methyl ester (TMRM) to identify and isolate metabolically robust T cells based on their mitochondrial membrane potential (ΔΨm). Comprehensive metabolomic and gene expression profiling demonstrated global features of improved metabolic fitness in low-ΔΨm-sorted CD8(+) T cells. Transfer of these low-ΔΨm T cells was associated with superior long-term in vivo persistence and an enhanced capacity to eradicate established tumors compared with high-ΔΨm cells. Use of ΔΨm-based sorting to enrich for cells with superior metabolic features was observed in CD8(+), CD4(+) T cell subsets, and long-term hematopoietic stem cells. This metabolism-based approach to cell selection may be broadly applicable to therapies involving the transfer of HSC or lymphocytes for the treatment of viral-associated illnesses and cancer.</p>","PeriodicalId":93927,"journal":{"name":"Cell metabolism","volume":"23 1","pages":"63-76"},"PeriodicalIF":30.9000,"publicationDate":"2016-01-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4747432/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Cell metabolism","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1016/j.cmet.2015.11.002","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2015/12/8 0:00:00","PubModel":"Epub","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Long-term survival and antitumor immunity of adoptively transferred CD8(+) T cells is dependent on their metabolic fitness, but approaches to isolate therapeutic T cells based on metabolic features are not well established. Here we utilized a lipophilic cationic dye tetramethylrhodamine methyl ester (TMRM) to identify and isolate metabolically robust T cells based on their mitochondrial membrane potential (ΔΨm). Comprehensive metabolomic and gene expression profiling demonstrated global features of improved metabolic fitness in low-ΔΨm-sorted CD8(+) T cells. Transfer of these low-ΔΨm T cells was associated with superior long-term in vivo persistence and an enhanced capacity to eradicate established tumors compared with high-ΔΨm cells. Use of ΔΨm-based sorting to enrich for cells with superior metabolic features was observed in CD8(+), CD4(+) T cell subsets, and long-term hematopoietic stem cells. This metabolism-based approach to cell selection may be broadly applicable to therapies involving the transfer of HSC or lymphocytes for the treatment of viral-associated illnesses and cancer.