Gradients of the signaling lipid S1P in lymph nodes position natural killer cells and regulate their interferon-γ response.
Victoria FangV Sai ChaluvadiWilly D Ramos-PerezAlejandra MendozaAudrey BaeyensRichard RiveraJerold ChunMichael CammerSusan R SchwabPublished in: Nature immunology (2016)
The lymph node periphery is an important site for many immunological functions, from pathogen containment to the differentiation of helper T cells, yet the cues that position cells in this region are largely undefined. Here, through the use of a reporter for the signaling lipid S1P (sphingosine 1-phosphate), we found that cells sensed higher concentrations of S1P in the medullary cords than in the T cell zone and that the S1P transporter SPNS2 on lymphatic endothelial cells generated this gradient. Natural killer (NK) cells are located at the periphery of the lymph node, predominantly in the medulla, and we found that expression of SPNS2, expression of the S1P receptor S1PR5 on NK cells, and expression of the chemokine receptor CXCR4 were all required for NK cell localization during homeostasis and rapid production of interferon-γ by NK cells after challenge. Our findings elucidate the spatial cues for NK cell organization and reveal a previously unknown role for S1P in positioning cells within the medulla.
Keyphrases
- nk cells
- lymph node
- induced apoptosis
- poor prognosis
- cell cycle arrest
- endothelial cells
- dendritic cells
- neoadjuvant chemotherapy
- binding protein
- sentinel lymph node
- endoplasmic reticulum stress
- long non coding rna
- natural killer cells
- regulatory t cells
- candida albicans
- radiation therapy
- african american
- vascular endothelial growth factor