Human CD4+ T cells require exogenous cystine for glutathione and DNA synthesis

// Trine B. Levring 1 , Martin Kongsbak 1 , Anna K. O. Rode 1 , Anders Woetmann 1 , Niels Ødum 1 , Charlotte Menné Bonefeld 1 , Carsten Geisler 1 1 Department of Immunology and Microbiology, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark Correspondence to: Carsten Geisler, e-mail: cge@sund.ku.dk Keywords: Immunology and Microbiology Section, Immune response, Immunity, T cell, cystine, glutathione, ribonucleotide reductase, DNA synthesis Received: July 07, 2015 Accepted: August 24, 2015 Published: September 03, 2015 ABSTRACT Adaptive immune responses require activation and expansion of antigen-specific T cells. Whereas early T cell activation is independent of exogenous cystine (Cys 2 ), T cell proliferation is dependent of Cys 2 . However, the exact roles of Cys 2 in T cell proliferation still need to be determined. The aim of this study was to elucidate why activated human T cells require exogenous Cys 2 in order to proliferate. We activated purified naïve human CD4 + T cells and found that glutathione (GSH) levels and DNA synthesis were dependent on Cys 2 and increased in parallel with increasing concentrations of Cys 2 . Vice-versa, the GSH synthesis inhibitor L-buthionine-sulfoximine (BSO) and inhibition of Cys 2 uptake with glutamate inhibited GSH and DNA synthesis in parallel. We further found that thioredoxin (Trx) can partly substitute for GSH during DNA synthesis. Finally, we show that GSH or Trx is required for the activity of ribonucleotide reductase (RNR), the enzyme responsible for generation of the deoxyribonucleotide DNA building blocks. In conclusion, we show that activated human T cells require exogenous Cys 2 to proliferate and that this is partly explained by the fact that Cys 2 is required for production of GSH, which in turn is required for optimal RNR-mediated deoxyribonucleotide synthesis and DNA replication.