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Clever-1 contributes to lymphocyte entry into the spleen via the red pulp.
Tadayon, Sina; Dunkel, Johannes; Takeda, Akira; Halle, Olga; Karikoski, Marika; Gerke, Heidi; Rantakari, Pia; Virtakoivu, Reetta; Pabst, Oliver; Salmi, Marko; Hollmén, Maija; Jalkanen, Sirpa.
Afiliación
  • Tadayon S; MediCity Research Laboratory and Institute of Biomedicine, University of Turku, 20520 Turku, Finland.
  • Dunkel J; MediCity Research Laboratory and Institute of Biomedicine, University of Turku, 20520 Turku, Finland.
  • Takeda A; MediCity Research Laboratory and Institute of Biomedicine, University of Turku, 20520 Turku, Finland.
  • Halle O; Institute of Immunology, Hannover Medical School, 30625 Hannover, Germany.
  • Karikoski M; MediCity Research Laboratory and Institute of Biomedicine, University of Turku, 20520 Turku, Finland.
  • Gerke H; MediCity Research Laboratory and Institute of Biomedicine, University of Turku, 20520 Turku, Finland.
  • Rantakari P; MediCity Research Laboratory and Institute of Biomedicine, University of Turku, 20520 Turku, Finland.
  • Virtakoivu R; MediCity Research Laboratory and Institute of Biomedicine, University of Turku, 20520 Turku, Finland.
  • Pabst O; Institute of Molecular Medicine, RWTH Aachen University, 52074 Aachen, Germany.
  • Salmi M; MediCity Research Laboratory and Institute of Biomedicine, University of Turku, 20520 Turku, Finland.
  • Hollmén M; MediCity Research Laboratory and Institute of Biomedicine, University of Turku, 20520 Turku, Finland.
  • Jalkanen S; MediCity Research Laboratory and Institute of Biomedicine, University of Turku, 20520 Turku, Finland. sirpa.jalkanen@utu.fi.
Sci Immunol ; 4(33)2019 03 29.
Article en En | MEDLINE | ID: mdl-30926591
ABSTRACT
Lymphocytes recirculate continuously between the blood and lymphoid organs, a process that is of fundamental importance for proper functioning of the immune system. The molecular mechanisms underlying lymphocyte trafficking to the spleen remain an enigma. Here, we show that lymphocytes enter the spleen preferentially from vessels in the red pulp rather than the marginal sinus or the vasculature in the white pulp. Ex vivo adhesion assays in mice and humans, together with genetic ablation of Clever-1 in mice, indicate that CD8+ T cell and B220+ B cell homing to the spleen via the red pulp is Clever-1 dependent. Moreover, absence of Clever-1 leads to down-regulation of the B cell attractant chemokine, CXCL13, on spleen endothelium. CXCL13 is known to guide B cell trafficking to lymphoid organs, and its lack may contribute to the observed decrease in B cell trafficking into the spleen as well. In summary, this study identifies Clever-1 as an important molecule controlling lymphocyte entry into the spleen, along with a critical role for the splenic red pulp in this regulated trafficking. Furthermore, the results demonstrate that location-specific homing-associated molecules guide lymphocyte entry into the spleen.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Bazo / Linfocitos / Moléculas de Adhesión Celular Neuronal / Receptores Mensajeros de Linfocitos Límite: Animals / Female / Humans / Male Idioma: En Revista: Sci Immunol Año: 2019 Tipo del documento: Article País de afiliación: Finlandia

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Bazo / Linfocitos / Moléculas de Adhesión Celular Neuronal / Receptores Mensajeros de Linfocitos Límite: Animals / Female / Humans / Male Idioma: En Revista: Sci Immunol Año: 2019 Tipo del documento: Article País de afiliación: Finlandia