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Endothelial and virgultar cell formations in the mammalian lymph node sinus: endothelial differentiation morphotypes characterized by a special kind of junction (complexus adhaerens)
Authors:Roland Moll  Evelyn Sievers  Bettina Hämmerling  Ansgar Schmidt  Mareike Barth  Caecilia Kuhn  Christine Grund  Ilse Hofmann  Werner W. Franke
Affiliation:(1) Institute of Pathology, Philipps University of Marburg, 35033 Marburg, Germany;(2) Division of Cell Biology, German Cancer Research Center (DKFZ), Im Neuenheimer Feld 280, 69120 Heidelberg, Germany;(3) Present address: Department of Ophthalmology, Heidelberg University School of Medicine, Im Neuenheimer Feld 400, 69120 Heidelberg, Germany;(4) Present address: Helmholtz Group for Cell Biology, German Cancer Research Center (DKFZ), Im Neuenheimer Feld 581, 69120 Heidelberg, Germany;(5) Present address: Joint Research Division of Vascular Biology of the Medical Faculty Mannheim, University of Heidelberg and the German Cancer Research Center (DKFZ), Ludolf-Krehl-Strasse 13–17, 68167 Mannheim, Germany
Abstract:The lymph node sinus are channel structures of unquestionable importance in immunology and pathology, specifically in the filtering of the lymph, the transport and processing of antigens, the adhesion and migration of immune cells, and the spread of metastatic cancer cells. Our knowledge of the cell and molecular biology of the sinus-forming cells is still limited, and the origin and biological nature of these cells have long been a matter of debate. Here, we review the relevant literature and present our own experimental results, in particular concerning molecular markers of intercellular junctions and cell differentiation. We show that both the monolayer cells lining the sinus walls and the intraluminal virgultar cell meshwork are indeed different morphotypes of the same basic endothelial cell character, as demonstrated by the presence of a distinct spectrum of general and lymphatic endothelial markers, and we therefore refer to these cells as sinus endothelial/virgultar cells (SEVCs). These cells are connected by unique adhering junctions, termed complexus adhaerentes, characterized by the transmembrane glycoprotein VE-cadherin, combined with the desmosomal plaque protein desmoplakin, several adherens junction plaque proteins including α- and β-catenin and p120 catenin, and components of the tight junction ensemble, specifically claudin-5 and JAM-A, and the plaque protein ZO-1. We show that complexus adhaerentes are involved in the tight three-dimensional integration of the virgultar network of SEVC processes along extracellular guidance structures composed of paracrystalline collagen bundle “stays”. Overall, the SEVC system might be considered as a local and specific modification of the general lymphatic vasculature system. Finally, physiological and pathological alterations of the SEVC system will be presented, and the possible value of the molecular markers described in histological diagnoses of autochthonous lymph node tumors will be discussed. Electronic supplementary material  The online version of this article (doi:) contains supplementary material, which is available to authorized users.
Contact Information Werner W. FrankeEmail:
Keywords:Sinus endothelial/virgultar cells (SEVCs)  Desmoplakin  CD31  Thrombomodulin  LYVE-1  VEGFR-3
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