Gremlin regulates renal inflammation via the vascular endothelial growth factor receptor 2 pathway. Issue 4 (19th May 2015)
- Record Type:
- Journal Article
- Title:
- Gremlin regulates renal inflammation via the vascular endothelial growth factor receptor 2 pathway. Issue 4 (19th May 2015)
- Main Title:
- Gremlin regulates renal inflammation via the vascular endothelial growth factor receptor 2 pathway
- Authors:
- Lavoz, Carolina
Alique, Matilde
Rodrigues‐Diez, Raquel
Pato, Janos
Keri, Gyorgy
Mezzano, Sergio
Egido, Jesús
Ruiz‐Ortega, Marta - Abstract:
- <abstract abstract-type="main" id="path4537-abs-0001"> <title>Abstract</title> <p id="path4537-para-0001">Inflammation is a main feature of progressive kidney disease. Gremlin binds to bone morphogenetic proteins (BMPs), acting as an antagonist and regulating nephrogenesis and fibrosis among other processes. Gremlin also binds to vascular endothelial growth factor receptor‐2 (VEGFR2) in endothelial cells to induce angiogenesis. In renal cells, gremlin regulates proliferation and fibrosis, but there are no data about inflammatory‐related events. We have investigated the direct effects of gremlin in the kidney, evaluating whether VEGFR2 is a functional gremlin receptor. Administration of recombinant gremlin to murine kidneys induced rapid and sustained activation of VEGFR2 signalling, located in proximal tubular epithelial cells. Gremlin bound to VEGFR2 in these cells <italic>in vitro</italic>, activating this signalling pathway independently of its action as an antagonist of BMPs. <italic>In vivo</italic>, gremlin caused early renal damage, characterized by activation of the nuclear factor (NF)‐κB pathway linked to up‐regulation of pro‐inflammatory factors and infiltration of immune inflammatory cells. VEGFR2 blockade diminished gremlin‐induced renal inflammatory responses. The link between gremlin/VEGFR2 and NF‐κB/inflammation was confirmed <italic>in vitro</italic>. Gremlin overexpression was associated with VEGFR2 activation in human renal disease and in the unilateral<abstract abstract-type="main" id="path4537-abs-0001"> <title>Abstract</title> <p id="path4537-para-0001">Inflammation is a main feature of progressive kidney disease. Gremlin binds to bone morphogenetic proteins (BMPs), acting as an antagonist and regulating nephrogenesis and fibrosis among other processes. Gremlin also binds to vascular endothelial growth factor receptor‐2 (VEGFR2) in endothelial cells to induce angiogenesis. In renal cells, gremlin regulates proliferation and fibrosis, but there are no data about inflammatory‐related events. We have investigated the direct effects of gremlin in the kidney, evaluating whether VEGFR2 is a functional gremlin receptor. Administration of recombinant gremlin to murine kidneys induced rapid and sustained activation of VEGFR2 signalling, located in proximal tubular epithelial cells. Gremlin bound to VEGFR2 in these cells <italic>in vitro</italic>, activating this signalling pathway independently of its action as an antagonist of BMPs. <italic>In vivo</italic>, gremlin caused early renal damage, characterized by activation of the nuclear factor (NF)‐κB pathway linked to up‐regulation of pro‐inflammatory factors and infiltration of immune inflammatory cells. VEGFR2 blockade diminished gremlin‐induced renal inflammatory responses. The link between gremlin/VEGFR2 and NF‐κB/inflammation was confirmed <italic>in vitro</italic>. Gremlin overexpression was associated with VEGFR2 activation in human renal disease and in the unilateral ureteral obstruction experimental model, where VEGFR2 kinase inhibition diminished renal inflammation. Our data show that a gremlin/VEGFR2 axis participates in renal inflammation and could be a novel target for kidney disease. Copyright © 2015 Pathological Society of Great Britain and Ireland. Published by John Wiley &amp; Sons, Ltd.</p> </abstract> … (more)
- Is Part Of:
- Journal of pathology. Volume 236:Issue 4(2015)
- Journal:
- Journal of pathology
- Issue:
- Volume 236:Issue 4(2015)
- Issue Display:
- Volume 236, Issue 4 (2015)
- Year:
- 2015
- Volume:
- 236
- Issue:
- 4
- Issue Sort Value:
- 2015-0236-0004-0000
- Page Start:
- 407
- Page End:
- 420
- Publication Date:
- 2015-05-19
- Subjects:
- Pathology -- Periodicals
616.07 - Journal URLs:
- http://onlinelibrary.wiley.com/ ↗
- DOI:
- 10.1002/path.4537 ↗
- Languages:
- English
- ISSNs:
- 0022-3417
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5029.900000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 2987.xml