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          Institute: MPI für molekulare Biomedizin     Collection: Jahrbuch 2016 (publ. 2015, arch)     Display Documents



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ID: 717259.0, MPI für molekulare Biomedizin / Jahrbuch 2016 (publ. 2015, arch)
cKit Lineage Hemogenic Endothelium-Derived Cells Contribute to Mesenteric Lymphatic Vessels
Authors:Stanczuk, L.; Martinez-Corral, I.; Ulvmar, M. H.; Zhang, Y.; Lavina, B.; Fruttiger, M.; Adams, R. H.; Saur, D.; Betsholtz, C.; Ortega, S.; Alitalo, K.; Graupera, M.; Makinen, T.
Date of Publication (YYYY-MM-DD):2015-03-10
Title of Journal:Cell Rep
Review Status:Internal review
Audience:Not Specified
Abstract / Description:Pathological lymphatic diseases mostly affect vessels in specific tissues, yet little is known about organ-specific regulation of the lymphatic vasculature. Here, we show that the vascular endothelial growth factor receptor 3 (VEGFR-3)/p110alpha PI3-kinase signaling pathway is selectively required for the formation of mesenteric lymphatic vasculature. Using genetic lineage tracing, we demonstrate that part of the mesenteric lymphatic vasculature develops from cKit lineage cells of hemogenic endothelial origin through a process we define as lymphvasculogenesis. This is contrary to the current dogma that all mammalian lymphatic vessels form by sprouting from veins. Our results reveal vascular-bed-specific differences in the origin and mechanisms of vessel formation, which may critically underlie organ-specific manifestation of lymphatic dysfunction in disease. The progenitor cells identified in this study may be exploited to restore lymphatic function following cancer surgery, lymphedema, or tissue trauma.
External Publication Status:published
Document Type:Article
Communicated by:Keuker
Affiliations:MPI für molekulare Biomedizin
External Affiliations:The Beijer Laboratory, Department of Immunology, Genetics and Pathology, Uppsala University, Dag Hammarskjoldsvag 20, 752 85 Uppsala, Sweden. UCL Institute of Ophthalmology, University College London (UCL), 11-43 Bath Street, London EC1V 9EL, UK. Department of Tissue Morphogenesis, Max Planck Institute for Molecular Biomedicine, and Faculty of Medicine, University of Munster, 48149 Munster, Germany. Department of Internal Medicine 2, Klinikum Rechts der Isar, Technische Universitat Munchen, Ismaningerstrasse 22, 81675 Munich, Germany; German Cancer Consortium (DKTK) and German Cancer Research Center (DKFZ), Im Neuenheimer Feld 280, 69120 Heidelberg, Germany. The Beijer Laboratory, Department of Immunology, Genetics and Pathology, Uppsala University, Dag Hammarskjoldsvag 20, 752 85 Uppsala, Sweden; Division of Vascular Biology, Department of Medical Biochemistry and Biophysics, Karolinska Institute, Scheeles Vag 2, 171 77 Stockholm, Sweden. Biotechnology Programme, Spanish National Cancer Research Centre, Melchor Fernandez Almagro 3, 28029 Madrid, Spain. Wihuri Research Institute and Translational Cancer Biology Program, Biomedicum Helsinki, University of Helsinki, Haartmaninkatu 8, 00014 Helsinki, Finland. Vascular Signalling Lab, IDIBELL, 3a planta - Gran Via de l'Hospitalet 199, L'Hospitalet de Llobregat, 08908 Barcelona, Spain. The Beijer Laboratory, Department of Immunology, Genetics and Pathology, Uppsala University, Dag Hammarskjoldsvag 20, 752 85 Uppsala, Sweden; Lymphatic Development Laboratory, Cancer Research UK London Research Institute (LRI), 44 Lincoln's Inn Fields, London WC2A 3LY, UK. Electronic address: taija.makinen@igp.uu.se.
Identifiers:ISSN:2211-1247 (Electronic) %R 10.1016/j.celrep.2015.02... [ID No:1]
URL:http://www.ncbi.nlm.nih.gov/pubmed/25772358 [ID No:2]
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