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Publication : The Lysophosphatidylcholine Transporter MFSD2A Is Essential for CD8<sup>+</sup> Memory T Cell Maintenance and Secondary Response to Infection.

First Author  Piccirillo AR Year  2019
Journal  J Immunol Volume  203
Issue  1 Pages  117-126
PubMed ID  31127034 Mgi Jnum  J:276960
Mgi Id  MGI:6315777 Doi  10.4049/jimmunol.1801585
Citation  Piccirillo AR, et al. (2019) The Lysophosphatidylcholine Transporter MFSD2A Is Essential for CD8(+) Memory T Cell Maintenance and Secondary Response to Infection. J Immunol 203(1):117-126
abstractText  Access to nutrients is critical for an effective T cell immune response to infection. Although transporters for sugars and amino acids have previously been described in the context of the CD8(+) T cell immune response, the active transport of exogenous fatty acids has remained enigmatic. In this study, we discovered that the sodium-dependent lysophosphatidylcholine (LPC) transporter major facilitator superfamily domain containing 2A (MFSD2A) is upregulated on activated CD8(+) T cells and is required for memory T cell maintenance. MFSD2A deficiency in mice resulted in decreased import of LPC esterified to long chain fatty acids into activated CD8(+) T cells, and MFSD2A-deficient cells are at a competitive disadvantage resulting in reduced memory T cell formation and maintenance and reduced response to secondary infection. Mechanistically, import of LPCs was required to maintain T cell homeostatic turnover, which when lost resulted in a decreased memory T cell pool and thus a reduced secondary response to repeat infection.
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