Document Detail


[Kidney transplantation: how shall we deal with marginal cases? Future prospects from basic research].
MedLine Citation:
PMID:  20808071     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
The research performed at the Department of Urology Osaka University Graduate School of Medicine is overviewed. Renal ischemia-reperfusion (I/R) injury is inevitable in transplantation and is related to longterm graft function. MF-1, a bifunctional hepatocyte growth factor-macrophage stimulating protein chimera, was found to prevent apoptosis. In our study, MF-1 directly guarded cultured proximal tubular epithelial cells from hypoxia-induced necrosis and apoptosis in vitro, and MF-1 treatment ameliorated renal dysfunction by preventing apoptosis in rat I/R injury model. The erythropoietin molecule modified by carbamylation (CEPO) has been identified and was demonstrated to protect several organs without increasing the hemoglobin concentration. The therapeutic effect of CEPO was evaluated using an endothelial tube formation assay, and a rat ischemia-reperfusion injury model. CEPO treatment induced more capillarylike formation than EPO. CEPO-treated kidneys showed minimal tubular apoptosis with increased peritubular capillary endothelial cells. We identified a new therapeutic approach using CEPO to protect the kidney from ischemia-reperfusion injury by promoting angiogenesis.
Authors:
Naotsugu Ichimaru; Koji Yazawa; Shiro Takahara
Publication Detail:
Type:  English Abstract; Journal Article; Review    
Journal Detail:
Title:  Hinyokika kiyo. Acta urologica Japonica     Volume:  56     ISSN:  0018-1994     ISO Abbreviation:  Hinyokika Kiyo     Publication Date:  2010 Aug 
Date Detail:
Created Date:  2010-09-02     Completed Date:  2010-11-04     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  0421145     Medline TA:  Hinyokika Kiyo     Country:  Japan    
Other Details:
Languages:  jpn     Pagination:  481-4     Citation Subset:  IM    
Affiliation:
Department of Specific Organ Regulation (Urology), Osaka University Graduate School of Medicine.
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MeSH Terms
Descriptor/Qualifier:
Animals
Cytokines / therapeutic use
Erythropoietin / analogs & derivatives,  therapeutic use
Graft Survival / physiology*
Hepatocyte Growth Factor / therapeutic use
Humans
Kidney Transplantation*
Rats
Recombinant Fusion Proteins / therapeutic use
Chemical
Reg. No./Substance:
0/Cytokines; 0/Recombinant Fusion Proteins; 0/carbamylated erythropoietin; 0/metron factor-1; 11096-26-7/Erythropoietin; 67256-21-7/Hepatocyte Growth Factor

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