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    Kidney international. 2019 Sep 3. pii: S0085-2538(19)30843-9. doi: 10.1016/j.kint.2019.07.027
    Lymphangiogenesis in a mouse model of renal transplant rejection extends life span of the recipients.
    Pedersen MS1,  Müller M2,  Rülicke T3,  Leitner N4,  Kain R5,  Regele H6,  Wang S7,  Gröne HJ8,  Rong S9,  Haller H10,  Gueler F11,  Rees AJ12,  Kerjaschki D13
    Author information
    1Department of Pathology, Medical University of Vienna, Vienna, Austria.
    2Institute of Animal Breeding and Genetics and Biomodels Austria, University of Veterinary Sciences, Vienna, Austria.
    3Institute of Laboratory Animal Science, University of Veterinary Medicine Vienna, Vienna, Austria.
    4Institute of Laboratory Animal Science, University of Veterinary Medicine Vienna, Vienna, Austria.
    5Department of Pathology, Medical University of Vienna, Vienna, Austria.
    6Department of Pathology, Medical University of Vienna, Vienna, Austria.
    7Department of Cellular and Molecular Pathology, Deutsches Krebsforschungszentrum Heidelberg, Heidelberg, Germany.
    8Department of Cellular and Molecular Pathology, Deutsches Krebsforschungszentrum Heidelberg, Heidelberg, Germany.
    9Department Nephrology, Medizinische Hochschule Hannover, Hannover, Germany.
    10Department Nephrology, Medizinische Hochschule Hannover, Hannover, Germany.
    11Department Nephrology, Medizinische Hochschule Hannover, Hannover, Germany.
    12Department of Pathology, Medical University of Vienna, Vienna, Austria. Electronic address: dontscho.kerjaschki@meduniwien.ac.at.
    13Department of Pathology, Medical University of Vienna, Vienna, Austria. Electronic address: andrew.rees@meduniwien.ac.at.
    Abstract

    Renal allograft rejection can be prevented by immunological tolerance, which may be associated with de novo formed lymphatic vessels in the donor kidney after transplantation in man. A suitable mouse model of renal allograft rejection in which lymphangiogenesis can be deliberately induced in the graft is critical for elucidating the mechanisms responsible for the association between attenuated transplant rejection and abundance of lymphatic vessels. Here we describe the development of a novel mouse model of rapid renal transplant rejection in which transgenic induction of lymphangiogenesis in the immune-incompatible graft greatly extends its survival time. Thus, our novel approach may facilitate exploitation of lymphangiogenesis in the grafted organ.


    Copyright © 2019 International Society of Nephrology. Published by Elsevier Inc. All rights reserved.

    KEYWORDS: immunological tolerance, lymphangiogenesis, mouse model, renal transplantation

    Publikations ID: 31718844
    Quelle: öffnen
     
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