Circadian clocks guide dendritic cells into skin lymphatics

[1]  A. Hidalgo,et al.  Circadian immune circuits , 2020, The Journal of experimental medicine.

[2]  N. Cermakian,et al.  The circadian clock of CD8 T cells modulates their early response to vaccination and the rhythmicity of related signaling pathways , 2019, Proceedings of the National Academy of Sciences.

[3]  Olga Tanaseichuk,et al.  Metascape provides a biologist-oriented resource for the analysis of systems-level datasets , 2019, Nature Communications.

[4]  Gaudenz Danuser,et al.  Nuclear positioning facilitates amoeboid migration along the path of least resistance , 2019, Nature.

[5]  D. Jackson Leucocyte Trafficking via the Lymphatic Vasculature— Mechanisms and Consequences , 2019, Front. Immunol..

[6]  M. Sperandio,et al.  Circadian Expression of Migratory Factors Establishes Lineage-Specific Signatures that Guide the Homing of Leukocyte Subsets to Tissues , 2018, Immunity.

[7]  Darren J. Fitzpatrick,et al.  Circadian clock protein BMAL1 regulates IL-1β in macrophages via NRF2 , 2018, Proceedings of the National Academy of Sciences.

[8]  A. Loudon,et al.  Clocking in to immunity , 2018, Nature Reviews Immunology.

[9]  D. Bechtold,et al.  The circadian regulator BMAL1 programmes responses to parasitic worm infection via a dendritic cell clock , 2018, Scientific Reports.

[10]  T. Hara,et al.  Glucocorticoids Drive Diurnal Oscillations in T Cell Distribution and Responses by Inducing Interleukin‐7 Receptor and CXCR4 , 2018, Immunity.

[11]  K. Mills,et al.  Loss of the molecular clock in myeloid cells exacerbates T cell-mediated CNS autoimmune disease , 2017, Nature Communications.

[12]  Vincenzo Cerundolo,et al.  Dendritic cells enter lymph vessels by hyaluronan-mediated docking to the endothelial receptor LYVE-1 , 2017, Nature Immunology.

[13]  H. Herzel,et al.  Lymphocyte Circadian Clocks Control Lymph Node Trafficking and Adaptive Immune Responses , 2017, Immunity.

[14]  Kazuhiro Suzuki,et al.  Adrenergic control of the adaptive immune response by diurnal lymphocyte recirculation through lymph nodes , 2016, The Journal of experimental medicine.

[15]  L. Santambrogio,et al.  Intralymphatic CCL21 Promotes Tissue Egress of Dendritic Cells through Afferent Lymphatic Vessels. , 2016, Cell reports.

[16]  Karl Mechtler,et al.  Polysialylation controls dendritic cell trafficking by regulating chemokine recognition , 2016, Science.

[17]  A. Loudon,et al.  An epithelial circadian clock controls pulmonary inflammation and glucocorticoid action , 2014, Nature Medicine.

[18]  T. Rülicke,et al.  The atypical chemokine receptor CCRL1 shapes functional CCL21 gradients in lymph nodes , 2014, Nature Immunology.

[19]  F. Naef,et al.  Circadian clock-dependent and -independent rhythmic proteomes implement distinct diurnal functions in mouse liver , 2013, Proceedings of the National Academy of Sciences.

[20]  S. Zelenay,et al.  Genetic Tracing via DNGR-1 Expression History Defines Dendritic Cells as a Hematopoietic Lineage , 2013, Cell.

[21]  C. Scheiermann,et al.  Circadian control of the immune system , 2013, Nature Reviews Immunology.

[22]  Michael Sixt,et al.  Interstitial Dendritic Cell Guidance by Haptotactic Chemokine Gradients , 2013, Science.

[23]  H. Strobl,et al.  Platelet endothelial cell adhesion molecule-1 (PECAM-1/CD31) and CD99 are critical in lymphatic transmigration of human dendritic cells. , 2012, The Journal of investigative dermatology.

[24]  D. Jackson,et al.  Inflammation-induced secretion of CCL21 in lymphatic endothelium is a key regulator of integrin-mediated dendritic cell transmigration. , 2010, International immunology.

[25]  M. Sixt,et al.  Preformed portals facilitate dendritic cell entry into afferent lymphatic vessels , 2009, The Journal of experimental medicine.

[26]  Thomas N. Sato,et al.  Increased DC trafficking to lymph nodes and contact hypersensitivity in junctional adhesion molecule-A-deficient mice. , 2004, The Journal of clinical investigation.

[27]  T. Blankenstein,et al.  CCR7 governs skin dendritic cell migration under inflammatory and steady-state conditions. , 2004, Immunity.

[28]  E. Wolf,et al.  CCR7 Coordinates the Primary Immune Response by Establishing Functional Microenvironments in Secondary Lymphoid Organs , 1999, Cell.

[29]  H. Saeki,et al.  Cutting edge: secondary lymphoid-tissue chemokine (SLC) and CC chemokine receptor 7 (CCR7) participate in the emigration pathway of mature dendritic cells from the skin to regional lymph nodes. , 1999, Journal of immunology.

[30]  U. Schibler,et al.  A Serum Shock Induces Circadian Gene Expression in Mammalian Tissue Culture Cells , 1998, Cell.

[31]  B. Stockinger,et al.  Mechanisms of tolerance induction in major histocompatibility complex class II-restricted T cells specific for a blood-borne self-antigen , 1994, The Journal of experimental medicine.

[32]  M. Sixt,et al.  In vitro analysis of chemotactic leukocyte migration in 3D environments. , 2011, Methods in molecular biology.

[33]  Seung Hyun Yoo INAUGURAL ARTICLE: PERIOD2::LUCIFERASE real-time reporting of circadian dynamics reveals persistent circadian oscillations in mouse peripheral tissues , 2004 .