1 In primed T cells, topographical memory is endowed by the stable expression of homing and chemokine receptors that promote their interactions with ligands expressed
by the endothelium of specific organs, such as the skin and the gut.7 Memory T cells with tropism for the skin are characterized by the expression of the carbohydrate epitope cutaneous lymphocyte antigen (CLA),10 and the chemokine receptors CCR411 and/or CCR10.12 CLA mediates the tethering and rolling of T cells through interaction with its endothelial counter-receptor, E-selectin, which is constitutively expressed on skin post-capillary venules. The ligands for CCR4 and CCR10, which are, respectively, chemokine (C-C motif) ligand DAPT solubility dmso 17 (CCL17) thymus and activation-regulated chemokine (TARC) and CCL27 cutaneous T cell-attracting chemokine (CTACK), have been found on inflamed and non-inflamed skin endothelium.11,13 CCL17 (TARC) was shown to selectively induce Erastin datasheet integrin-dependent adhesion to intercellular adhesion molecule 1 (ICAM-1) of skin-derived memory T cells under static conditions and under physiological flow,11 while CCL27 (CTACK) was found to be preferentially produced by epidermal keratinocytes, and its chemotactic effect
on T cells was demonstrated in in vitro assays.13 Constitutive memory T-cell trafficking into the lamina propria of the small intestine requires the interaction of the integrin α4β7 and the chemokine receptor CCR9 on the lymphocyte surface14 with mucosal vascular addressin cell adhesion molecule 1 (MAdCAM-1) and CCL25 thymus-expressed chemokine (TECK) on endothelial cells of gut lamina propria venules, respectively.15 T cells lacking β7-integrin chain expression are severely impaired in their ability to localize to the intestinal mucosa16 and CCL25 blockade or genetic ablation of CCR9 significantly reduces antigen-specific Protein Tyrosine Kinase inhibitor CD8+ T-cell migration to the small
intestine.17 Additional adhesion molecules, such as vascular adhesion protein-1 (VAP-118) and CD44,19 may contribute to a significant diversity of potential address codes, but selectins, α4-integrins, β2-integrins, and chemokine receptors and their respective ligands appear to be the workhorses of the system with differential but broadly overlapping functions at the various destinations of lymphocyte trafficking. The paradigm of organ-specific homing is based on the assumption that T-cell priming within a specific tissue environment, such as cutaneous and mesenteric lymph nodes (MLNs), leads to an imprinting of the expression of specific homing receptors.17,20,21 Recent studies have shown that tissue-derived dendritic cells (DCs) are key mediators of the induction of T-cell tissue-specific homing potential.