CTGF Inhibits BMP-7 Signaling in Diabetic Nephropathy

In diabetic nephropathy, connective tissue growth factor (CTGF) is upregulated and bone morphogenetic protein 7 (BMP-7) is downregulated. CTGF is known to inhibit BMP-4, but similar cross-talk between BMP-7 and CTGF has not been studied. In this study, it was hypothesized that CTGF acts as an inhibi...

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Veröffentlicht in:Journal of the American Society of Nephrology 2008-11, Vol.19 (11), p.2098-2107
Hauptverfasser: NGUYEN, Tri Q, ROESTENBERG, Peggy, BRANDAN, Enrique, LYONS, Karen M, GOLDSCHMEDING, Roel, VAN NIEUWENHOVEN, Frans A, BOVENSCHEN, Niels, ZEKE LI, XU, Leon, OLIVER, Noelynn, ATEN, Jan, JOLES, Jaap A, VIAL, Cecilia
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container_issue 11
container_start_page 2098
container_title Journal of the American Society of Nephrology
container_volume 19
creator NGUYEN, Tri Q
ROESTENBERG, Peggy
BRANDAN, Enrique
LYONS, Karen M
GOLDSCHMEDING, Roel
VAN NIEUWENHOVEN, Frans A
BOVENSCHEN, Niels
ZEKE LI
XU, Leon
OLIVER, Noelynn
ATEN, Jan
JOLES, Jaap A
VIAL, Cecilia
description In diabetic nephropathy, connective tissue growth factor (CTGF) is upregulated and bone morphogenetic protein 7 (BMP-7) is downregulated. CTGF is known to inhibit BMP-4, but similar cross-talk between BMP-7 and CTGF has not been studied. In this study, it was hypothesized that CTGF acts as an inhibitor of BMP-7 signaling activity in diabetic nephropathy. Compared with diabetic wild-type CTGF(+/+) mice, diabetic CTGF(+/-) mice had approximately 50% lower CTGF mRNA and protein, less severe albuminuria, no thickening of the glomerular basement membrane, and preserved matrix metalloproteinase (MMP) activity. Although the amount of BMP-7 mRNA was similar in the kidneys of diabetic CTGF(+/+) and CTGF(+/-) mice, phosphorylation of the BMP signal transduction protein Smad1/5 and expression of the BMP target gene Id1 were lower in diabetic CTGF(+/+) mice. Moreover, renal Id1 mRNA expression correlated with albuminuria (R = -0.86) and MMP activity (R = 0.76). In normoglycemic mice, intraperitoneal injection of CTGF led to a decrease of pSmad1/5 in the renal cortex. In cultured renal glomerular and tubulointerstitial cells, CTGF diminished BMP-7 signaling activity, evidenced by lower levels of pSmad1/5, Id1 mRNA, and BMP-responsive element-luciferase activity. Co-immunoprecipitation, solid-phase binding assay, and surface plasmon resonance analysis showed that CTGF binds BMP-7 with high affinity (Kd approximately 14 nM). In conclusion, upregulation of CTGF inhibits BMP-7 signal transduction in the diabetic kidney and contributes to altered gene transcription, reduced MMP activity, glomerular basement membrane thickening, and albuminuria, all of which are hallmarks of diabetic nephropathy.
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CTGF is known to inhibit BMP-4, but similar cross-talk between BMP-7 and CTGF has not been studied. In this study, it was hypothesized that CTGF acts as an inhibitor of BMP-7 signaling activity in diabetic nephropathy. Compared with diabetic wild-type CTGF(+/+) mice, diabetic CTGF(+/-) mice had approximately 50% lower CTGF mRNA and protein, less severe albuminuria, no thickening of the glomerular basement membrane, and preserved matrix metalloproteinase (MMP) activity. Although the amount of BMP-7 mRNA was similar in the kidneys of diabetic CTGF(+/+) and CTGF(+/-) mice, phosphorylation of the BMP signal transduction protein Smad1/5 and expression of the BMP target gene Id1 were lower in diabetic CTGF(+/+) mice. Moreover, renal Id1 mRNA expression correlated with albuminuria (R = -0.86) and MMP activity (R = 0.76). In normoglycemic mice, intraperitoneal injection of CTGF led to a decrease of pSmad1/5 in the renal cortex. In cultured renal glomerular and tubulointerstitial cells, CTGF diminished BMP-7 signaling activity, evidenced by lower levels of pSmad1/5, Id1 mRNA, and BMP-responsive element-luciferase activity. Co-immunoprecipitation, solid-phase binding assay, and surface plasmon resonance analysis showed that CTGF binds BMP-7 with high affinity (Kd approximately 14 nM). In conclusion, upregulation of CTGF inhibits BMP-7 signal transduction in the diabetic kidney and contributes to altered gene transcription, reduced MMP activity, glomerular basement membrane thickening, and albuminuria, all of which are hallmarks of diabetic nephropathy.</description><identifier>ISSN: 1046-6673</identifier><identifier>EISSN: 1533-3450</identifier><identifier>DOI: 10.1681/asn.2007111261</identifier><identifier>PMID: 18632843</identifier><identifier>CODEN: JASNEU</identifier><language>eng</language><publisher>Hagerstown, MD: Lippincott Williams &amp; Wilkins</publisher><subject>Animals ; Associated diseases and complications ; Basic Research ; Biological and medical sciences ; Bone Morphogenetic Protein 7 ; Bone Morphogenetic Proteins - deficiency ; Bone Morphogenetic Proteins - genetics ; Bone Morphogenetic Proteins - physiology ; Connective Tissue Growth Factor ; Diabetes Mellitus, Experimental - genetics ; Diabetes Mellitus, Experimental - pathology ; Diabetes Mellitus, Experimental - physiopathology ; Diabetes. Impaired glucose tolerance ; Diabetic Nephropathies - genetics ; Diabetic Nephropathies - pathology ; Diabetic Nephropathies - physiopathology ; Endocrine pancreas. Apud cells (diseases) ; Endocrinopathies ; Female ; Gene Expression ; Immediate-Early Proteins - deficiency ; Immediate-Early Proteins - genetics ; Immediate-Early Proteins - pharmacology ; Immediate-Early Proteins - physiology ; Inhibitor of Differentiation Protein 1 - genetics ; Intercellular Signaling Peptides and Proteins - deficiency ; Intercellular Signaling Peptides and Proteins - genetics ; Intercellular Signaling Peptides and Proteins - pharmacology ; Intercellular Signaling Peptides and Proteins - physiology ; Kidney - metabolism ; Kidney - pathology ; Kidneys ; Male ; Medical sciences ; Mice ; Mice, Inbred BALB C ; Mice, Inbred C57BL ; Mice, Knockout ; Nephrology. Urinary tract diseases ; Protein Binding ; Recombinant Proteins - pharmacology ; RNA, Messenger - genetics ; RNA, Messenger - metabolism ; Signal Transduction ; Smad1 Protein - metabolism ; Smad5 Protein - metabolism ; Transforming Growth Factor beta - deficiency ; Transforming Growth Factor beta - genetics ; Transforming Growth Factor beta - physiology ; Urinary system involvement in other diseases. Miscellaneous</subject><ispartof>Journal of the American Society of Nephrology, 2008-11, Vol.19 (11), p.2098-2107</ispartof><rights>2008 INIST-CNRS</rights><rights>Copyright © 2008 by the American Society of Nephrology</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c529t-41b752c007e5e3bc53ef816f06b0a2577e97592624ddbd37743f323f41e004763</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC2573007/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC2573007/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,315,729,782,786,887,27931,27932,53798,53800</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=20833392$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18632843$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>NGUYEN, Tri Q</creatorcontrib><creatorcontrib>ROESTENBERG, Peggy</creatorcontrib><creatorcontrib>BRANDAN, Enrique</creatorcontrib><creatorcontrib>LYONS, Karen M</creatorcontrib><creatorcontrib>GOLDSCHMEDING, Roel</creatorcontrib><creatorcontrib>VAN NIEUWENHOVEN, Frans A</creatorcontrib><creatorcontrib>BOVENSCHEN, Niels</creatorcontrib><creatorcontrib>ZEKE LI</creatorcontrib><creatorcontrib>XU, Leon</creatorcontrib><creatorcontrib>OLIVER, Noelynn</creatorcontrib><creatorcontrib>ATEN, Jan</creatorcontrib><creatorcontrib>JOLES, Jaap A</creatorcontrib><creatorcontrib>VIAL, Cecilia</creatorcontrib><title>CTGF Inhibits BMP-7 Signaling in Diabetic Nephropathy</title><title>Journal of the American Society of Nephrology</title><addtitle>J Am Soc Nephrol</addtitle><description>In diabetic nephropathy, connective tissue growth factor (CTGF) is upregulated and bone morphogenetic protein 7 (BMP-7) is downregulated. CTGF is known to inhibit BMP-4, but similar cross-talk between BMP-7 and CTGF has not been studied. In this study, it was hypothesized that CTGF acts as an inhibitor of BMP-7 signaling activity in diabetic nephropathy. Compared with diabetic wild-type CTGF(+/+) mice, diabetic CTGF(+/-) mice had approximately 50% lower CTGF mRNA and protein, less severe albuminuria, no thickening of the glomerular basement membrane, and preserved matrix metalloproteinase (MMP) activity. Although the amount of BMP-7 mRNA was similar in the kidneys of diabetic CTGF(+/+) and CTGF(+/-) mice, phosphorylation of the BMP signal transduction protein Smad1/5 and expression of the BMP target gene Id1 were lower in diabetic CTGF(+/+) mice. Moreover, renal Id1 mRNA expression correlated with albuminuria (R = -0.86) and MMP activity (R = 0.76). In normoglycemic mice, intraperitoneal injection of CTGF led to a decrease of pSmad1/5 in the renal cortex. In cultured renal glomerular and tubulointerstitial cells, CTGF diminished BMP-7 signaling activity, evidenced by lower levels of pSmad1/5, Id1 mRNA, and BMP-responsive element-luciferase activity. Co-immunoprecipitation, solid-phase binding assay, and surface plasmon resonance analysis showed that CTGF binds BMP-7 with high affinity (Kd approximately 14 nM). In conclusion, upregulation of CTGF inhibits BMP-7 signal transduction in the diabetic kidney and contributes to altered gene transcription, reduced MMP activity, glomerular basement membrane thickening, and albuminuria, all of which are hallmarks of diabetic nephropathy.</description><subject>Animals</subject><subject>Associated diseases and complications</subject><subject>Basic Research</subject><subject>Biological and medical sciences</subject><subject>Bone Morphogenetic Protein 7</subject><subject>Bone Morphogenetic Proteins - deficiency</subject><subject>Bone Morphogenetic Proteins - genetics</subject><subject>Bone Morphogenetic Proteins - physiology</subject><subject>Connective Tissue Growth Factor</subject><subject>Diabetes Mellitus, Experimental - genetics</subject><subject>Diabetes Mellitus, Experimental - pathology</subject><subject>Diabetes Mellitus, Experimental - physiopathology</subject><subject>Diabetes. Impaired glucose tolerance</subject><subject>Diabetic Nephropathies - genetics</subject><subject>Diabetic Nephropathies - pathology</subject><subject>Diabetic Nephropathies - physiopathology</subject><subject>Endocrine pancreas. Apud cells (diseases)</subject><subject>Endocrinopathies</subject><subject>Female</subject><subject>Gene Expression</subject><subject>Immediate-Early Proteins - deficiency</subject><subject>Immediate-Early Proteins - genetics</subject><subject>Immediate-Early Proteins - pharmacology</subject><subject>Immediate-Early Proteins - physiology</subject><subject>Inhibitor of Differentiation Protein 1 - genetics</subject><subject>Intercellular Signaling Peptides and Proteins - deficiency</subject><subject>Intercellular Signaling Peptides and Proteins - genetics</subject><subject>Intercellular Signaling Peptides and Proteins - pharmacology</subject><subject>Intercellular Signaling Peptides and Proteins - physiology</subject><subject>Kidney - metabolism</subject><subject>Kidney - pathology</subject><subject>Kidneys</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Mice</subject><subject>Mice, Inbred BALB C</subject><subject>Mice, Inbred C57BL</subject><subject>Mice, Knockout</subject><subject>Nephrology. Urinary tract diseases</subject><subject>Protein Binding</subject><subject>Recombinant Proteins - pharmacology</subject><subject>RNA, Messenger - genetics</subject><subject>RNA, Messenger - metabolism</subject><subject>Signal Transduction</subject><subject>Smad1 Protein - metabolism</subject><subject>Smad5 Protein - metabolism</subject><subject>Transforming Growth Factor beta - deficiency</subject><subject>Transforming Growth Factor beta - genetics</subject><subject>Transforming Growth Factor beta - physiology</subject><subject>Urinary system involvement in other diseases. Miscellaneous</subject><issn>1046-6673</issn><issn>1533-3450</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVkMFPwjAUxhujEUSvHs0uehu2fWu7XUwQBUkQTcBz03Ud1IwO12HCf-8MC-jpveT93vd9-RC6JrhPeEzulXd9irEghFBOTlCXMIAQIoZPmx1HPORcQAddeP-JMWFUiHPUITEHGkfQRWy4GI-CiVvZ1NY-eHx9D0Uwt0unCuuWgXXBk1Wpqa0OZmazqsqNqle7S3SWq8Kbq3b20MfoeTF8Cadv48lwMA01o0kdRiQVjOomnmEGUs3A5DHhOeYpVpQJYRLBEspplGVpBkJEkAOFPCIG40hw6KGHve5mm65Npo2rK1XITWXXqtrJUln5_-LsSi7Lb9mIQ2PbCNy1AlX5tTW-lmvrtSkK5Uy59ZIngsQiYQ3Y34O6Kr2vTH4wIVj-Ni0H85k8Nt083PyNdsTbahvgtgWU16rIK-W09QeO4hgAEgo_bOeEMA</recordid><startdate>20081101</startdate><enddate>20081101</enddate><creator>NGUYEN, Tri Q</creator><creator>ROESTENBERG, Peggy</creator><creator>BRANDAN, Enrique</creator><creator>LYONS, Karen M</creator><creator>GOLDSCHMEDING, Roel</creator><creator>VAN NIEUWENHOVEN, Frans A</creator><creator>BOVENSCHEN, Niels</creator><creator>ZEKE LI</creator><creator>XU, Leon</creator><creator>OLIVER, Noelynn</creator><creator>ATEN, Jan</creator><creator>JOLES, Jaap A</creator><creator>VIAL, Cecilia</creator><general>Lippincott Williams &amp; Wilkins</general><general>American Society of Nephrology</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20081101</creationdate><title>CTGF Inhibits BMP-7 Signaling in Diabetic Nephropathy</title><author>NGUYEN, Tri Q ; ROESTENBERG, Peggy ; BRANDAN, Enrique ; LYONS, Karen M ; GOLDSCHMEDING, Roel ; VAN NIEUWENHOVEN, Frans A ; BOVENSCHEN, Niels ; ZEKE LI ; XU, Leon ; OLIVER, Noelynn ; ATEN, Jan ; JOLES, Jaap A ; VIAL, Cecilia</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c529t-41b752c007e5e3bc53ef816f06b0a2577e97592624ddbd37743f323f41e004763</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Animals</topic><topic>Associated diseases and complications</topic><topic>Basic Research</topic><topic>Biological and medical sciences</topic><topic>Bone Morphogenetic Protein 7</topic><topic>Bone Morphogenetic Proteins - deficiency</topic><topic>Bone Morphogenetic Proteins - genetics</topic><topic>Bone Morphogenetic Proteins - physiology</topic><topic>Connective Tissue Growth Factor</topic><topic>Diabetes Mellitus, Experimental - genetics</topic><topic>Diabetes Mellitus, Experimental - pathology</topic><topic>Diabetes Mellitus, Experimental - physiopathology</topic><topic>Diabetes. Impaired glucose tolerance</topic><topic>Diabetic Nephropathies - genetics</topic><topic>Diabetic Nephropathies - pathology</topic><topic>Diabetic Nephropathies - physiopathology</topic><topic>Endocrine pancreas. Apud cells (diseases)</topic><topic>Endocrinopathies</topic><topic>Female</topic><topic>Gene Expression</topic><topic>Immediate-Early Proteins - deficiency</topic><topic>Immediate-Early Proteins - genetics</topic><topic>Immediate-Early Proteins - pharmacology</topic><topic>Immediate-Early Proteins - physiology</topic><topic>Inhibitor of Differentiation Protein 1 - genetics</topic><topic>Intercellular Signaling Peptides and Proteins - deficiency</topic><topic>Intercellular Signaling Peptides and Proteins - genetics</topic><topic>Intercellular Signaling Peptides and Proteins - pharmacology</topic><topic>Intercellular Signaling Peptides and Proteins - physiology</topic><topic>Kidney - metabolism</topic><topic>Kidney - pathology</topic><topic>Kidneys</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Mice</topic><topic>Mice, Inbred BALB C</topic><topic>Mice, Inbred C57BL</topic><topic>Mice, Knockout</topic><topic>Nephrology. Urinary tract diseases</topic><topic>Protein Binding</topic><topic>Recombinant Proteins - pharmacology</topic><topic>RNA, Messenger - genetics</topic><topic>RNA, Messenger - metabolism</topic><topic>Signal Transduction</topic><topic>Smad1 Protein - metabolism</topic><topic>Smad5 Protein - metabolism</topic><topic>Transforming Growth Factor beta - deficiency</topic><topic>Transforming Growth Factor beta - genetics</topic><topic>Transforming Growth Factor beta - physiology</topic><topic>Urinary system involvement in other diseases. 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CTGF is known to inhibit BMP-4, but similar cross-talk between BMP-7 and CTGF has not been studied. In this study, it was hypothesized that CTGF acts as an inhibitor of BMP-7 signaling activity in diabetic nephropathy. Compared with diabetic wild-type CTGF(+/+) mice, diabetic CTGF(+/-) mice had approximately 50% lower CTGF mRNA and protein, less severe albuminuria, no thickening of the glomerular basement membrane, and preserved matrix metalloproteinase (MMP) activity. Although the amount of BMP-7 mRNA was similar in the kidneys of diabetic CTGF(+/+) and CTGF(+/-) mice, phosphorylation of the BMP signal transduction protein Smad1/5 and expression of the BMP target gene Id1 were lower in diabetic CTGF(+/+) mice. Moreover, renal Id1 mRNA expression correlated with albuminuria (R = -0.86) and MMP activity (R = 0.76). In normoglycemic mice, intraperitoneal injection of CTGF led to a decrease of pSmad1/5 in the renal cortex. In cultured renal glomerular and tubulointerstitial cells, CTGF diminished BMP-7 signaling activity, evidenced by lower levels of pSmad1/5, Id1 mRNA, and BMP-responsive element-luciferase activity. Co-immunoprecipitation, solid-phase binding assay, and surface plasmon resonance analysis showed that CTGF binds BMP-7 with high affinity (Kd approximately 14 nM). In conclusion, upregulation of CTGF inhibits BMP-7 signal transduction in the diabetic kidney and contributes to altered gene transcription, reduced MMP activity, glomerular basement membrane thickening, and albuminuria, all of which are hallmarks of diabetic nephropathy.</abstract><cop>Hagerstown, MD</cop><pub>Lippincott Williams &amp; Wilkins</pub><pmid>18632843</pmid><doi>10.1681/asn.2007111261</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record>
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source MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central
subjects Animals
Associated diseases and complications
Basic Research
Biological and medical sciences
Bone Morphogenetic Protein 7
Bone Morphogenetic Proteins - deficiency
Bone Morphogenetic Proteins - genetics
Bone Morphogenetic Proteins - physiology
Connective Tissue Growth Factor
Diabetes Mellitus, Experimental - genetics
Diabetes Mellitus, Experimental - pathology
Diabetes Mellitus, Experimental - physiopathology
Diabetes. Impaired glucose tolerance
Diabetic Nephropathies - genetics
Diabetic Nephropathies - pathology
Diabetic Nephropathies - physiopathology
Endocrine pancreas. Apud cells (diseases)
Endocrinopathies
Female
Gene Expression
Immediate-Early Proteins - deficiency
Immediate-Early Proteins - genetics
Immediate-Early Proteins - pharmacology
Immediate-Early Proteins - physiology
Inhibitor of Differentiation Protein 1 - genetics
Intercellular Signaling Peptides and Proteins - deficiency
Intercellular Signaling Peptides and Proteins - genetics
Intercellular Signaling Peptides and Proteins - pharmacology
Intercellular Signaling Peptides and Proteins - physiology
Kidney - metabolism
Kidney - pathology
Kidneys
Male
Medical sciences
Mice
Mice, Inbred BALB C
Mice, Inbred C57BL
Mice, Knockout
Nephrology. Urinary tract diseases
Protein Binding
Recombinant Proteins - pharmacology
RNA, Messenger - genetics
RNA, Messenger - metabolism
Signal Transduction
Smad1 Protein - metabolism
Smad5 Protein - metabolism
Transforming Growth Factor beta - deficiency
Transforming Growth Factor beta - genetics
Transforming Growth Factor beta - physiology
Urinary system involvement in other diseases. Miscellaneous
title CTGF Inhibits BMP-7 Signaling in Diabetic Nephropathy
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