Human podocytes express angiopoietin 1, a potential regulator of glomerular vascular endothelial growth factor

Vascular endothelial growth factor (VEGF) is abundantly expressed by podocytes, but its role in glomeruli is unknown. Angiopoietins are endothelial cell growth factors that function in concert with VEGF but have not previously been observed in human glomeruli. Angiopoietin 1 (Ang1) acts via the endo...

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Veröffentlicht in:Journal of the American Society of Nephrology 2002-02, Vol.13 (2), p.544-550
Hauptverfasser: SATCHELL, Simon C, HARPER, Steve J, TOOKE, John E, KERJASCHKI, Dontscho, SALEEM, Moin A, MATHIESON, Peter W
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container_issue 2
container_start_page 544
container_title Journal of the American Society of Nephrology
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creator SATCHELL, Simon C
HARPER, Steve J
TOOKE, John E
KERJASCHKI, Dontscho
SALEEM, Moin A
MATHIESON, Peter W
description Vascular endothelial growth factor (VEGF) is abundantly expressed by podocytes, but its role in glomeruli is unknown. Angiopoietins are endothelial cell growth factors that function in concert with VEGF but have not previously been observed in human glomeruli. Angiopoietin 1 (Ang1) acts via the endothelial receptor Tie2 to promote maturation and stabilization of blood vessels, resisting angiogenesis and opposing some actions of VEGF. Ang1, Ang2, Tie2, and VEGF expression in normal human renal cortex was examined with immunofluorescence and immunohistochemical analyses. High-power, multiple-color, immunofluorescence analyses and additional antibodies (specific for particular components of the glomerular filtration barrier) were used to determine the exact locations of Ang1 and Tie2 in the glomerular capillary wall. Immuno-electron-microscopic analysis of rat glomeruli was used to further localize endothelial Tie2 expression. RNA and protein extracted from human glomeruli, cultured human podocytes, and cultured human endothelial cells were analyzed for Ang1, Ang2, and Tie2 by using reverse transcription-PCR and Western blotting. Ang1 was detected in podocytes in normal glomeruli and, with VEGF, was concentrated in podocyte foot processes. Tie2 was demonstrated on glomerular capillary endothelial cells, particularly on the abluminal surface. Reverse transcription-PCR and Western blotting analyses confirmed the expression of Ang1 and Tie2 in glomeruli and of Ang1 in cultured podocytes. These findings suggest a role for Ang1 in the maintenance of the glomerular endothelium and make it a good candidate to be a regulator of the actions of VEGF on glomerular permeability, resisting angiogenesis while allowing the induction of high permeability to water and small solutes.
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Angiopoietins are endothelial cell growth factors that function in concert with VEGF but have not previously been observed in human glomeruli. Angiopoietin 1 (Ang1) acts via the endothelial receptor Tie2 to promote maturation and stabilization of blood vessels, resisting angiogenesis and opposing some actions of VEGF. Ang1, Ang2, Tie2, and VEGF expression in normal human renal cortex was examined with immunofluorescence and immunohistochemical analyses. High-power, multiple-color, immunofluorescence analyses and additional antibodies (specific for particular components of the glomerular filtration barrier) were used to determine the exact locations of Ang1 and Tie2 in the glomerular capillary wall. Immuno-electron-microscopic analysis of rat glomeruli was used to further localize endothelial Tie2 expression. RNA and protein extracted from human glomeruli, cultured human podocytes, and cultured human endothelial cells were analyzed for Ang1, Ang2, and Tie2 by using reverse transcription-PCR and Western blotting. Ang1 was detected in podocytes in normal glomeruli and, with VEGF, was concentrated in podocyte foot processes. Tie2 was demonstrated on glomerular capillary endothelial cells, particularly on the abluminal surface. Reverse transcription-PCR and Western blotting analyses confirmed the expression of Ang1 and Tie2 in glomeruli and of Ang1 in cultured podocytes. 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RNA and protein extracted from human glomeruli, cultured human podocytes, and cultured human endothelial cells were analyzed for Ang1, Ang2, and Tie2 by using reverse transcription-PCR and Western blotting. Ang1 was detected in podocytes in normal glomeruli and, with VEGF, was concentrated in podocyte foot processes. Tie2 was demonstrated on glomerular capillary endothelial cells, particularly on the abluminal surface. Reverse transcription-PCR and Western blotting analyses confirmed the expression of Ang1 and Tie2 in glomeruli and of Ang1 in cultured podocytes. 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Psychology</topic><topic>Humans</topic><topic>Immunohistochemistry</topic><topic>Kidney Cortex - cytology</topic><topic>Kidney Cortex - metabolism</topic><topic>Kidney Glomerulus - metabolism</topic><topic>Lymphokines - metabolism</topic><topic>Membrane Glycoproteins - metabolism</topic><topic>Membrane Glycoproteins - physiology</topic><topic>Microscopy, Immunoelectron</topic><topic>Proteins - metabolism</topic><topic>Receptor Protein-Tyrosine Kinases - metabolism</topic><topic>Receptor, TIE-2</topic><topic>Reverse Transcriptase Polymerase Chain Reaction</topic><topic>Vascular Endothelial Growth Factor A</topic><topic>Vascular Endothelial Growth Factors</topic><topic>Vertebrates: urinary system</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>SATCHELL, Simon C</creatorcontrib><creatorcontrib>HARPER, Steve J</creatorcontrib><creatorcontrib>TOOKE, John E</creatorcontrib><creatorcontrib>KERJASCHKI, Dontscho</creatorcontrib><creatorcontrib>SALEEM, Moin A</creatorcontrib><creatorcontrib>MATHIESON, Peter W</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of the American Society of Nephrology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>SATCHELL, Simon C</au><au>HARPER, Steve J</au><au>TOOKE, John E</au><au>KERJASCHKI, Dontscho</au><au>SALEEM, Moin A</au><au>MATHIESON, Peter W</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Human podocytes express angiopoietin 1, a potential regulator of glomerular vascular endothelial growth factor</atitle><jtitle>Journal of the American Society of Nephrology</jtitle><addtitle>J Am Soc Nephrol</addtitle><date>2002-02-01</date><risdate>2002</risdate><volume>13</volume><issue>2</issue><spage>544</spage><epage>550</epage><pages>544-550</pages><issn>1046-6673</issn><eissn>1533-3450</eissn><coden>JASNEU</coden><abstract>Vascular endothelial growth factor (VEGF) is abundantly expressed by podocytes, but its role in glomeruli is unknown. 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subjects Angiopoietin-1
Angiopoietin-2
Biological and medical sciences
Blotting, Western
Cells, Cultured
Endothelial Growth Factors - metabolism
Fundamental and applied biological sciences. Psychology
Humans
Immunohistochemistry
Kidney Cortex - cytology
Kidney Cortex - metabolism
Kidney Glomerulus - metabolism
Lymphokines - metabolism
Membrane Glycoproteins - metabolism
Membrane Glycoproteins - physiology
Microscopy, Immunoelectron
Proteins - metabolism
Receptor Protein-Tyrosine Kinases - metabolism
Receptor, TIE-2
Reverse Transcriptase Polymerase Chain Reaction
Vascular Endothelial Growth Factor A
Vascular Endothelial Growth Factors
Vertebrates: urinary system
title Human podocytes express angiopoietin 1, a potential regulator of glomerular vascular endothelial growth factor
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