Skip Navigation


NDT Advance Access originally published online on December 22, 2005
Nephrology Dialysis Transplantation 2006 21(3):568-573; doi:10.1093/ndt/gfk010
This Article
Right arrow Full Text Freely available
Right arrow FREE Full Text (PDF) Freely available
Right arrow All Versions of this Article:
21/3/568    most recent
gfk010v1
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrow Search for citing articles in:
ISI Web of Science (14)
Right arrowRequest Permissions
Right arrow Disclaimer
Google Scholar
Right arrow Articles by Zeisberg, M.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Zeisberg, M.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

© The Author [2005]. Published by Oxford University Press on behalf of ERA-EDTA. All rights reserved. For Permissions, please email: journals.permissions@oxfordjournals.org


Editorial Comment

Bone morphogenic protein-7 and the kidney: current concepts and open questions

Michael Zeisberg

Center for Matrix Biology, Department of Medicine, Beth Israel Deaconess Medical Center, Boston, MA 02215, USA

Correspondence and offprint requests to: Dr Michael Zeisberg, Center for Matrix Biology, Beth Israel Deaconess Medical Centre, Harvard Medical School, 330 Brookline Avenue, RW511, Boston, MA 02215. Email: mzeisber@bidmc.harvard.edu

Keywords: Bone Morphogenic Protein-7 (BMP-7); Fibrosis; Epithelial Mesenchymal Transition (EMT); Chronic Kidney Disease (CKD); Chronic Renal Failure (CRF)

The first 150 words of the full text of this article appear below.



   Introduction
 
Several recent studies have demonstrated unequivocally that administration of bone morphogenic protein-7 (BMP-7) has a therapeutic effect in various animal models of acute and chronic renal injury (Table 1). However, the underlying mechanisms of BMP-7 action in the kidney remained largely unknown in these initial reports. Here, novel aspects regarding the biology of BMP-7 in the kidney will be discussed.


View this table:
[in this window]
[in a new window]
 
Table 1. Published studies, which demonstrated a therapeutic effect of recombinant BMP-7 in animal models of chronic renal disease

 


   What is BMP-7?
 
BMP-7, also known as Osteogenic protein-1 (OP-1), is one of 15 currently known BMPs, which are structurally and functionally related and which are part of the transforming growth factor ß (TGF-ß) superfamily of growth factors [1]. BMP-7 was originally identified as a regulator of cartilage and bone formation [2]. However, BMPs have also been shown to regulate the growth, differentiation, chemotaxis and apoptosis of various cell types, . . . [Full Text of this Article]



   What is the role of BMP-7 in the developing kidney?
 


   How does BMP-7 protect the kidney from injury?
 


   How is the biological activity of endogenous BMP-7 in the kidney regulated?
 


   Is there a role for kidney derived BMP-7 outside the kidney?
 


   How can these insights into the biology of BMP-7 impact on clinical nephrology?
 

Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
J. Am. Soc. Nephrol.Home page
M.-A Yu, K.-S. Shin, J. H. Kim, Y.-I. Kim, S. S. Chung, S.-H. Park, Y.-L. Kim, and D.-H. Kang
HGF and BMP-7 Ameliorate High Glucose-Induced Epithelial-to-Mesenchymal Transition of Peritoneal Mesothelium
J. Am. Soc. Nephrol., March 1, 2009; 20(3): 567 - 581.
[Abstract] [Full Text] [PDF]


Home page
J. Am. Soc. Nephrol.Home page
T. Q. Nguyen, P. Roestenberg, F. A. van Nieuwenhoven, N. Bovenschen, Z. Li, L. Xu, N. Oliver, J. Aten, J. A. Joles, C. Vial, et al.
CTGF Inhibits BMP-7 Signaling in Diabetic Nephropathy
J. Am. Soc. Nephrol., November 1, 2008; 19(11): 2098 - 2107.
[Abstract] [Full Text] [PDF]


Home page
Nephrol Dial TransplantHome page
P. Boor, K. Sebekova, T. Ostendorf, and J. Floege
Treatment targets in renal fibrosis
Nephrol. Dial. Transplant., December 1, 2007; 22(12): 3391 - 3407.
[Full Text] [PDF]


Home page
Nephrol Dial TransplantHome page
S. Mezzano, A. Droguett, M. Eugenia Burgos, C. Aros, L. Ardiles, C. Flores, D. Carpio, G. Carvajal, M. Ruiz-Ortega, and J. Egido
Expression of gremlin, a bone morphogenetic protein antagonist, in glomerular crescents of pauci-immune glomerulonephritis
Nephrol. Dial. Transplant., July 1, 2007; 22(7): 1882 - 1890.
[Abstract] [Full Text] [PDF]


Home page
DiabetesHome page
H. Sugimoto, G. Grahovac, M. Zeisberg, and R. Kalluri
Renal Fibrosis and Glomerulosclerosis in a New Mouse Model of Diabetic Nephropathy and Its Regression by Bone Morphogenic Protein-7 and Advanced Glycation End Product Inhibitors
Diabetes, July 1, 2007; 56(7): 1825 - 1833.
[Abstract] [Full Text] [PDF]