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Lymphangiogenesis in a mouse model of renal transplant rejection extends life span of the recipients.
Pedersen, Mads S; Müller, Mathias; Rülicke, Thomas; Leitner, Nicole; Kain, Renate; Regele, Heinz; Wang, Shijun; Gröne, Hermann-Josef; Rong, Song; Haller, Hermann; Gueler, Faikah; Rees, Andrew J; Kerjaschki, Dontscho.
Afiliação
  • Pedersen MS; Department of Pathology, Medical University of Vienna, Vienna, Austria.
  • Müller M; Institute of Animal Breeding and Genetics and Biomodels Austria, University of Veterinary Sciences, Vienna, Austria.
  • Rülicke T; Institute of Laboratory Animal Science, University of Veterinary Medicine Vienna, Vienna, Austria.
  • Leitner N; Institute of Laboratory Animal Science, University of Veterinary Medicine Vienna, Vienna, Austria.
  • Kain R; Department of Pathology, Medical University of Vienna, Vienna, Austria.
  • Regele H; Department of Pathology, Medical University of Vienna, Vienna, Austria.
  • Wang S; Department of Cellular and Molecular Pathology, Deutsches Krebsforschungszentrum Heidelberg, Heidelberg, Germany.
  • Gröne HJ; Department of Cellular and Molecular Pathology, Deutsches Krebsforschungszentrum Heidelberg, Heidelberg, Germany.
  • Rong S; Department Nephrology, Medizinische Hochschule Hannover, Hannover, Germany.
  • Haller H; Department Nephrology, Medizinische Hochschule Hannover, Hannover, Germany.
  • Gueler F; Department Nephrology, Medizinische Hochschule Hannover, Hannover, Germany.
  • Rees AJ; Department of Pathology, Medical University of Vienna, Vienna, Austria. Electronic address: andrew.rees@meduniwien.ac.at.
  • Kerjaschki D; Department of Pathology, Medical University of Vienna, Vienna, Austria. Electronic address: dontscho.kerjaschki@meduniwien.ac.at.
Kidney Int ; 97(1): 89-94, 2020 01.
Article em En | MEDLINE | ID: mdl-31718844
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.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Transplante de Rim / Linfangiogênese / Rejeição de Enxerto / Sobrevivência de Enxerto / Nefropatias Tipo de estudo: Prognostic_studies Limite: Animals / Female / Humans / Male Idioma: En Revista: Kidney Int Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Áustria

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Transplante de Rim / Linfangiogênese / Rejeição de Enxerto / Sobrevivência de Enxerto / Nefropatias Tipo de estudo: Prognostic_studies Limite: Animals / Female / Humans / Male Idioma: En Revista: Kidney Int Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Áustria