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Inflammation switches the chemoattractant requirements for naive lymphocyte entry into lymph nodes
Cell ( IF 45.5 ) Pub Date : 2024-12-20 , DOI: 10.1016/j.cell.2024.11.031 Kevin Y. Chen, Marco De Giovanni, Ying Xu, Jinping An, Nikhita Kirthivasan, Erick Lu, Kan Jiang, Stephen Brooks, Serena Ranucci, Jiuling Yang, Shuto Kanameishi, Kenji Kabashima, Kevin Brulois, Michael Bscheider, Eugene C. Butcher, Jason G. Cyster
Cell ( IF 45.5 ) Pub Date : 2024-12-20 , DOI: 10.1016/j.cell.2024.11.031 Kevin Y. Chen, Marco De Giovanni, Ying Xu, Jinping An, Nikhita Kirthivasan, Erick Lu, Kan Jiang, Stephen Brooks, Serena Ranucci, Jiuling Yang, Shuto Kanameishi, Kenji Kabashima, Kevin Brulois, Michael Bscheider, Eugene C. Butcher, Jason G. Cyster
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Sustained lymphocyte migration from blood into lymph nodes (LNs) is important for immune responses. The CC-chemokine receptor-7 (CCR7) ligand CCL21 is required for LN entry but is downregulated during inflammation, and it has been unclear how recruitment is maintained. Here, we show that the oxysterol biosynthetic enzyme cholesterol-25-hydroxylase (Ch25h) is upregulated in LN high endothelial venules during viral infection. Lymphocytes become dependent on oxysterols, generated through a transcellular endothelial-fibroblast metabolic pathway, and the receptor EBI2 for inflamed LN entry. Additionally, Langerhans cells are an oxysterol source. Ch25h is also expressed in inflamed peripheral endothelium, and EBI2 mediates B cell recruitment in a tumor model. Finally, we demonstrate that LN CCL19 is critical in lymphocyte recruitment during inflammation. Thus, our work explains how naive precursor trafficking is sustained in responding LNs, identifies a role for oxysterols in cell recruitment into inflamed tissues, and establishes a logic for the CCR7 two-ligand system.
更新日期：2024-12-20
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