Myeloid-Derived Suppressor Cells Inhibit T-Cell Activation by Depleting Cystine and Cysteine
Louisiana State University Health Sciences Center New Orleans · University of Maryland, Baltimore County
Abstract
Myeloid-derived suppressor cells (MDSC) are present in most cancer patients and are potent inhibitors of T-cell-mediated antitumor immunity. Their inhibitory activity is attributed to production of arginase, reactive oxygen species, inducible nitric oxide synthase, and interleukin-10. Here we show that MDSCs also block T-cell activation by sequestering cystine and limiting the availability of cysteine. Cysteine is an essential amino acid for T-cell activation because T cells lack cystathionase, which converts methionine to cysteine, and because they do not have an intact xc- transporter and therefore cannot import cystine and reduce it intracellularly to cysteine. T cells depend on antigen-presenting cells…
Citation impact
- FWCI
- 15.49
- Percentile
- 100%
- References
- 47
Authors
5- MKMinu K. Srivastava
Louisiana State University Health Sciences Center New Orleans, University of Maryland, Baltimore County
- PSPratima Sinha
Louisiana State University Health Sciences Center New Orleans, University of Maryland, Baltimore County
- VKVirginia K. Clements
Louisiana State University Health Sciences Center New Orleans, University of Maryland, Baltimore County
- PCPaulo C. Rodrı́guez
Louisiana State University Health Sciences Center New Orleans, University of Maryland, Baltimore County
- SOSuzanne Ostrand‐RosenbergCorresponding
Louisiana State University Health Sciences Center New Orleans, University of Maryland, Baltimore County
Topics & keywords
- Cysteine
- Cystine
- Biochemistry
- Chemistry
- T cell
- Extracellular
- Cysteine metabolism
- Cell biology