Mitochondrial Membrane Potential Identifies Cells with Enhanced Stemness for Cellular Therapy

Cell Metab. 2016 Jan 12;23(1):63-76. doi: 10.1016/j.cmet.2015.11.002. Epub 2015 Dec 8.

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.

Publication types

  • Research Support, N.I.H., Intramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • CD8-Positive T-Lymphocytes / physiology
  • Cell Line, Tumor
  • Cytokines / physiology
  • Hematopoietic Stem Cells / physiology
  • Humans
  • Lymphoid Progenitor Cells / physiology*
  • Lymphoid Progenitor Cells / transplantation
  • Melanoma, Experimental / therapy*
  • Membrane Potential, Mitochondrial*
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Neoplasm Transplantation
  • Oxidative Stress
  • Stem Cell Transplantation
  • T-Lymphocyte Subsets / physiology*
  • T-Lymphocyte Subsets / transplantation
  • Transcriptome

Substances

  • Cytokines