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Literature summary for 3.4.21.73 extracted from

  • Gueler, F.; Rong, S.; Mengel, M.; Park, J.K.; Kiyan, J.; Kirsch, T.; Dumler, I.; Haller, H.; Shushakova, N.
    Renal urokinase-type plasminogen activator (uPA) receptor but not uPA deficiency strongly attenuates ischemia reperfusion injury and acute kidney allograft rejection (2008), J. Immunol., 181, 1179-1189.
    View publication on PubMed

Application

Application Comment Organism
medicine in mice model for kidney ischemia reperfusion injury, deficiency for uPA receptor, but not uPA protects from ischemia reperfusion injury. In the allogenic kidney transplant model, uPA receptor but not uPA deficiency of the allograft causes superior recipient survival and strongly attenuates loss of renal function. uPA receptor-deficient allografts show reduced generation of reactive oxygen species and apoptosis. Neutrophil and monocyte/macrophage infiltration is strongly attenuated and up-regulation of the adhesion molecule ICAM-1 is completely abrogated in uPA receptor-deficient allografts Mus musculus

Organism

Organism UniProt Comment Textmining
Mus musculus
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mice model for kidney ischemia reperfusion injury and for acute kidney allograft rejection
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Source Tissue

Source Tissue Comment Organism Textmining
kidney in mice model for kidney ischemia reperfusion injury, deficiency for uPA receptor, but not uPA protects from ischemia reperfusion injury. In the allogenic kidney transplant model, uPA receptor but not uPA deficiency of the allograft causes superior recipient survival and strongly attenuates loss of renal function Mus musculus
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