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血管生成素-1疗法会加剧叶酸诱导的急性肾损伤后的纤维化和炎症反应。

Angiopoietin-1 therapy enhances fibrosis and inflammation following folic acid-induced acute renal injury.

作者信息

Long David A, Price Karen L, Ioffe Ella, Gannon Claire M, Gnudi Luigi, White Kathryn E, Yancopoulos George D, Rudge John S, Woolf Adrian S

机构信息

Nephro-Urology Unit, University College London, Institute of Child Health, London, UK.

出版信息

Kidney Int. 2008 Aug;74(3):300-9. doi: 10.1038/ki.2008.179. Epub 2008 May 14.

Abstract

The loss of interstitial capillaries is a feature of several experimental models of renal disease and this contributes to secondary kidney injury. Angiopoietin-1 is a secreted growth factor which binds to Tie-2 present on endothelia to enhance cell survival thereby stabilizing capillary architecture in-vitro. Previous studies showed that angiopoietin-1 prevented renal capillary and interstitial lesions following experimental ureteric obstruction. We tested here the effect of angiopoietin-1 treatment on capillary loss and associated tubulointerstitial damage known to follow recovery from folic acid-induced tubular necrosis and acute renal injury. We found that delivery of angiopoietin-1 by adenoviral vectors stabilized peritubular capillaries in folic acid nephropathy but this was accompanied by profibrotic and inflammatory effects. These results suggest that the use of endothelial growth factor therapy for kidney disease may have varying outcomes that depend on the disease model tested.

摘要

间质毛细血管的丧失是几种肾脏疾病实验模型的一个特征,这会导致继发性肾损伤。血管生成素-1是一种分泌型生长因子,它与内皮细胞上的Tie-2结合,以提高细胞存活率,从而在体外稳定毛细血管结构。先前的研究表明,血管生成素-1可预防实验性输尿管梗阻后的肾毛细血管和间质损伤。我们在此测试了血管生成素-1治疗对已知在叶酸诱导的肾小管坏死和急性肾损伤恢复后出现的毛细血管丧失及相关肾小管间质损伤的影响。我们发现,通过腺病毒载体递送血管生成素-1可稳定叶酸肾病中的肾小管周围毛细血管,但这伴随着促纤维化和炎症效应。这些结果表明,针对肾脏疾病使用内皮生长因子疗法可能会有不同的结果,这取决于所测试的疾病模型。

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