Angiopoietin-1 therapy enhances fibrosis and inflammation following folic acid-induced acute renal injury
Author(s) -
David A. Long,
Karen Price,
Ella Ioffe,
Claire M. Gan,
Luigi Gnudi,
Kathryn White,
George D. Yancopoulos,
John S. Rudge,
Adrian S. Woolf
Publication year - 2008
Publication title -
kidney international
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.499
H-Index - 276
eISSN - 1523-1755
pISSN - 0085-2538
DOI - 10.1038/ki.2008.179
Subject(s) - medicine , fibrosis , acute kidney injury , kidney disease , nephropathy , kidney , inflammation , angiopoietin , pathology , vascular endothelial growth factor , endocrinology , diabetes mellitus , vegf receptors
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.
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