Dexamethasone Induces Connective Tissue Growth Factor Expression in Renal Tubular Epithelial Cells in a Mouse Strain-Specific Manner
Connective tissue growth factor (CTGF), a downstream mediator of transforming growth factor-β1, mediates mesangial cell/fibroblast proliferation and extracellular matrix production by renal cells. Here, we show that renal tubular epithelial cells from patients with minimal change nephritic syndrome...
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description | Connective tissue growth factor (CTGF), a downstream mediator of transforming growth factor-β1, mediates mesangial cell/fibroblast proliferation and extracellular matrix production by renal cells. Here, we show that renal tubular epithelial cells from patients with minimal change nephritic syndrome produced CTGF after glucocorticoid treatment. In addition, the glucocorticoid dexamethasone (DEX) increased CTGF mRNA levels in the kidneys of C57B6 but not SJL mice and produced intermediate CTGF mRNA levels in the kidneys of F1 (C57B6 × SJL) mice, midway between the levels found for parental strains. DEX also increased CTGF mRNA levels in cultured tubular epithelial cells derived from C57B6 (mProx24) but not SJL (MCT) mice via transcriptional up-regulation of CTGF mRNA. Transient transfection experiments using luciferase reporter constructs bearing CTGF promoter fragments revealed that the −897- to −628-bp fragment contained DEX-responsive positive regulatory elements, which were active in mProx24 but not MCT cells. Long-term DEX treatment resulted in fibronectin deposition in the kidneys of C57B6 but not SJL mice, and this effect was inhibited by co-administration of CTGF anti-sense oligodeoxynucleotides. Thus, glucocorticoid-induced renal fibrogenesis seems to be influenced by genetic background, with the critical DEX-responsive elements in the −897- to −628-bp region of the CTGF promoter. |
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Here, we show that renal tubular epithelial cells from patients with minimal change nephritic syndrome produced CTGF after glucocorticoid treatment. In addition, the glucocorticoid dexamethasone (DEX) increased CTGF mRNA levels in the kidneys of C57B6 but not SJL mice and produced intermediate CTGF mRNA levels in the kidneys of F1 (C57B6 × SJL) mice, midway between the levels found for parental strains. DEX also increased CTGF mRNA levels in cultured tubular epithelial cells derived from C57B6 (mProx24) but not SJL (MCT) mice via transcriptional up-regulation of CTGF mRNA. Transient transfection experiments using luciferase reporter constructs bearing CTGF promoter fragments revealed that the −897- to −628-bp fragment contained DEX-responsive positive regulatory elements, which were active in mProx24 but not MCT cells. Long-term DEX treatment resulted in fibronectin deposition in the kidneys of C57B6 but not SJL mice, and this effect was inhibited by co-administration of CTGF anti-sense oligodeoxynucleotides. Thus, glucocorticoid-induced renal fibrogenesis seems to be influenced by genetic background, with the critical DEX-responsive elements in the −897- to −628-bp region of the CTGF promoter.</description><identifier>ISSN: 0002-9440</identifier><identifier>EISSN: 1525-2191</identifier><identifier>DOI: 10.2353/ajpath.2006.050656</identifier><identifier>PMID: 16507889</identifier><identifier>CODEN: AJPAA4</identifier><language>eng</language><publisher>Bethesda, MD: Elsevier Inc</publisher><subject>Adolescent ; Adult ; Animals ; Base Sequence ; Biological and medical sciences ; Connective Tissue Growth Factor ; Dexamethasone - pharmacology ; Epithelial Cells - chemistry ; Epithelial Cells - drug effects ; Epithelial Cells - metabolism ; Female ; Fibronectins - analysis ; Fibronectins - metabolism ; Genes, Reporter ; Humans ; Immediate-Early Proteins - analysis ; Immediate-Early Proteins - biosynthesis ; Immediate-Early Proteins - genetics ; Intercellular Signaling Peptides and Proteins - analysis ; Intercellular Signaling Peptides and Proteins - biosynthesis ; Intercellular Signaling Peptides and Proteins - genetics ; Investigative techniques, diagnostic techniques (general aspects) ; Kidney Tubules - drug effects ; Kidney Tubules - metabolism ; Kidney Tubules - pathology ; Luciferases - analysis ; Luciferases - genetics ; Male ; Medical sciences ; Mice ; Mice, Inbred Strains ; Molecular Sequence Data ; Nephritis - genetics ; Nephritis - metabolism ; Nephritis - pathology ; Oligodeoxyribonucleotides, Antisense - pharmacology ; Original Research Paper ; Pathology. Cytology. Biochemistry. Spectrometry. Miscellaneous investigative techniques ; Promoter Regions, Genetic ; RNA, Messenger - analysis ; RNA, Messenger - metabolism ; Syndrome ; Transcription, Genetic - drug effects ; Up-Regulation</subject><ispartof>The American journal of pathology, 2006-03, Vol.168 (3), p.737-747</ispartof><rights>2006 American Society for Investigative Pathology</rights><rights>2006 INIST-CNRS</rights><rights>Copyright © American Society for Investigative Pathology 2006</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c580t-fcb82184820d992166205a8b6a332ad209815b8a7c1dd1f68ca7649b3008de103</citedby><cites>FETCH-LOGICAL-c580t-fcb82184820d992166205a8b6a332ad209815b8a7c1dd1f68ca7649b3008de103</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC1606512/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://dx.doi.org/10.2353/ajpath.2006.050656$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>230,314,724,777,781,882,3537,27905,27906,45976,53772,53774</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=17670964$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16507889$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Okada, Hirokazu</creatorcontrib><creatorcontrib>Kikuta, Tomohiro</creatorcontrib><creatorcontrib>Inoue, Tsutomu</creatorcontrib><creatorcontrib>Kanno, Yoshihiko</creatorcontrib><creatorcontrib>Ban, Shinichi</creatorcontrib><creatorcontrib>Sugaya, Takeshi</creatorcontrib><creatorcontrib>Takigawa, Masaharu</creatorcontrib><creatorcontrib>Suzuki, Hiromichi</creatorcontrib><title>Dexamethasone Induces Connective Tissue Growth Factor Expression in Renal Tubular Epithelial Cells in a Mouse Strain-Specific Manner</title><title>The American journal of pathology</title><addtitle>Am J Pathol</addtitle><description>Connective tissue growth factor (CTGF), a downstream mediator of transforming growth factor-β1, mediates mesangial cell/fibroblast proliferation and extracellular matrix production by renal cells. Here, we show that renal tubular epithelial cells from patients with minimal change nephritic syndrome produced CTGF after glucocorticoid treatment. In addition, the glucocorticoid dexamethasone (DEX) increased CTGF mRNA levels in the kidneys of C57B6 but not SJL mice and produced intermediate CTGF mRNA levels in the kidneys of F1 (C57B6 × SJL) mice, midway between the levels found for parental strains. DEX also increased CTGF mRNA levels in cultured tubular epithelial cells derived from C57B6 (mProx24) but not SJL (MCT) mice via transcriptional up-regulation of CTGF mRNA. Transient transfection experiments using luciferase reporter constructs bearing CTGF promoter fragments revealed that the −897- to −628-bp fragment contained DEX-responsive positive regulatory elements, which were active in mProx24 but not MCT cells. Long-term DEX treatment resulted in fibronectin deposition in the kidneys of C57B6 but not SJL mice, and this effect was inhibited by co-administration of CTGF anti-sense oligodeoxynucleotides. Thus, glucocorticoid-induced renal fibrogenesis seems to be influenced by genetic background, with the critical DEX-responsive elements in the −897- to −628-bp region of the CTGF promoter.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Animals</subject><subject>Base Sequence</subject><subject>Biological and medical sciences</subject><subject>Connective Tissue Growth Factor</subject><subject>Dexamethasone - pharmacology</subject><subject>Epithelial Cells - chemistry</subject><subject>Epithelial Cells - drug effects</subject><subject>Epithelial Cells - metabolism</subject><subject>Female</subject><subject>Fibronectins - analysis</subject><subject>Fibronectins - metabolism</subject><subject>Genes, Reporter</subject><subject>Humans</subject><subject>Immediate-Early Proteins - analysis</subject><subject>Immediate-Early Proteins - biosynthesis</subject><subject>Immediate-Early Proteins - genetics</subject><subject>Intercellular Signaling Peptides and Proteins - analysis</subject><subject>Intercellular Signaling Peptides and Proteins - biosynthesis</subject><subject>Intercellular Signaling Peptides and Proteins - genetics</subject><subject>Investigative techniques, diagnostic techniques (general aspects)</subject><subject>Kidney Tubules - drug effects</subject><subject>Kidney Tubules - metabolism</subject><subject>Kidney Tubules - pathology</subject><subject>Luciferases - analysis</subject><subject>Luciferases - genetics</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Mice</subject><subject>Mice, Inbred Strains</subject><subject>Molecular Sequence Data</subject><subject>Nephritis - genetics</subject><subject>Nephritis - metabolism</subject><subject>Nephritis - pathology</subject><subject>Oligodeoxyribonucleotides, Antisense - pharmacology</subject><subject>Original Research Paper</subject><subject>Pathology. Cytology. Biochemistry. Spectrometry. Miscellaneous investigative techniques</subject><subject>Promoter Regions, Genetic</subject><subject>RNA, Messenger - analysis</subject><subject>RNA, Messenger - metabolism</subject><subject>Syndrome</subject><subject>Transcription, Genetic - drug effects</subject><subject>Up-Regulation</subject><issn>0002-9440</issn><issn>1525-2191</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kUFv1DAQhSMEotvCH-CAfIFbFttJHEdCSGhpS6VWSHQ5WxNn0rjK2sFOtuXeH46jrFi4cLLs-ebNG78kecPommdF9gHuBxi7NadUrGlBRSGeJStW8CLlrGLPkxWllKdVntOT5DSE-3gVmaQvkxMmClpKWa2Spy_4CDscOwjOIrmyzaQxkI2zFvVo9ki2JoQJyaV3D2NHLkCPzpPzx8FjCMZZYiz5jhZ6sp3qqYdYG8zYYW_i0wb7PswEkBs3BSS3owdj09sBtWmNJjcQ5_hXyYsW-oCvD-dZ8uPifLv5ml5_u7zafL5OdSHpmLa6lpzJXHLaVBVnQnBagKwFZBmHhtNKsqKWUGrWNKwVUkMp8qrOKJUNMpqdJZ8W3WGqd9hotNFOrwZvduB_KQdG_VuxplN3bq-YiL_LeBR4fxDw7ueEYVQ7E3RcEizG_ZQoS8p5PoN8AbV3IXhs_wxhVM3hqSU8NYenlvBi09u_7R1bDmlF4N0BgKChbz1YbcKRK0VJK5EfbXbmrnswHlXYQd9HWTbPZUKqTJVZGcGPC4jx1_cGvQraoNXYxCY9qsaZ_xn-DXUEx3k</recordid><startdate>20060301</startdate><enddate>20060301</enddate><creator>Okada, Hirokazu</creator><creator>Kikuta, Tomohiro</creator><creator>Inoue, Tsutomu</creator><creator>Kanno, Yoshihiko</creator><creator>Ban, Shinichi</creator><creator>Sugaya, Takeshi</creator><creator>Takigawa, Masaharu</creator><creator>Suzuki, Hiromichi</creator><general>Elsevier Inc</general><general>ASIP</general><general>American Society for Investigative Pathology</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>20060301</creationdate><title>Dexamethasone Induces Connective Tissue Growth Factor Expression in Renal Tubular Epithelial Cells in a Mouse Strain-Specific Manner</title><author>Okada, Hirokazu ; Kikuta, Tomohiro ; Inoue, Tsutomu ; Kanno, Yoshihiko ; Ban, Shinichi ; Sugaya, Takeshi ; Takigawa, Masaharu ; Suzuki, Hiromichi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c580t-fcb82184820d992166205a8b6a332ad209815b8a7c1dd1f68ca7649b3008de103</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Animals</topic><topic>Base Sequence</topic><topic>Biological and medical sciences</topic><topic>Connective Tissue Growth Factor</topic><topic>Dexamethasone - pharmacology</topic><topic>Epithelial Cells - chemistry</topic><topic>Epithelial Cells - drug effects</topic><topic>Epithelial Cells - metabolism</topic><topic>Female</topic><topic>Fibronectins - analysis</topic><topic>Fibronectins - metabolism</topic><topic>Genes, Reporter</topic><topic>Humans</topic><topic>Immediate-Early Proteins - analysis</topic><topic>Immediate-Early Proteins - biosynthesis</topic><topic>Immediate-Early Proteins - genetics</topic><topic>Intercellular Signaling Peptides and Proteins - analysis</topic><topic>Intercellular Signaling Peptides and Proteins - biosynthesis</topic><topic>Intercellular Signaling Peptides and Proteins - genetics</topic><topic>Investigative techniques, diagnostic techniques (general aspects)</topic><topic>Kidney Tubules - drug effects</topic><topic>Kidney Tubules - metabolism</topic><topic>Kidney Tubules - pathology</topic><topic>Luciferases - analysis</topic><topic>Luciferases - genetics</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Mice</topic><topic>Mice, Inbred Strains</topic><topic>Molecular Sequence Data</topic><topic>Nephritis - genetics</topic><topic>Nephritis - metabolism</topic><topic>Nephritis - pathology</topic><topic>Oligodeoxyribonucleotides, Antisense - pharmacology</topic><topic>Original Research Paper</topic><topic>Pathology. Cytology. Biochemistry. Spectrometry. Miscellaneous investigative techniques</topic><topic>Promoter Regions, Genetic</topic><topic>RNA, Messenger - analysis</topic><topic>RNA, Messenger - metabolism</topic><topic>Syndrome</topic><topic>Transcription, Genetic - drug effects</topic><topic>Up-Regulation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Okada, Hirokazu</creatorcontrib><creatorcontrib>Kikuta, Tomohiro</creatorcontrib><creatorcontrib>Inoue, Tsutomu</creatorcontrib><creatorcontrib>Kanno, Yoshihiko</creatorcontrib><creatorcontrib>Ban, Shinichi</creatorcontrib><creatorcontrib>Sugaya, Takeshi</creatorcontrib><creatorcontrib>Takigawa, Masaharu</creatorcontrib><creatorcontrib>Suzuki, Hiromichi</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><collection>PubMed Central (Full Participant titles)</collection><jtitle>The American journal of pathology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Okada, Hirokazu</au><au>Kikuta, Tomohiro</au><au>Inoue, Tsutomu</au><au>Kanno, Yoshihiko</au><au>Ban, Shinichi</au><au>Sugaya, Takeshi</au><au>Takigawa, Masaharu</au><au>Suzuki, Hiromichi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Dexamethasone Induces Connective Tissue Growth Factor Expression in Renal Tubular Epithelial Cells in a Mouse Strain-Specific Manner</atitle><jtitle>The American journal of pathology</jtitle><addtitle>Am J Pathol</addtitle><date>2006-03-01</date><risdate>2006</risdate><volume>168</volume><issue>3</issue><spage>737</spage><epage>747</epage><pages>737-747</pages><issn>0002-9440</issn><eissn>1525-2191</eissn><coden>AJPAA4</coden><abstract>Connective tissue growth factor (CTGF), a downstream mediator of transforming growth factor-β1, mediates mesangial cell/fibroblast proliferation and extracellular matrix production by renal cells. Here, we show that renal tubular epithelial cells from patients with minimal change nephritic syndrome produced CTGF after glucocorticoid treatment. In addition, the glucocorticoid dexamethasone (DEX) increased CTGF mRNA levels in the kidneys of C57B6 but not SJL mice and produced intermediate CTGF mRNA levels in the kidneys of F1 (C57B6 × SJL) mice, midway between the levels found for parental strains. DEX also increased CTGF mRNA levels in cultured tubular epithelial cells derived from C57B6 (mProx24) but not SJL (MCT) mice via transcriptional up-regulation of CTGF mRNA. Transient transfection experiments using luciferase reporter constructs bearing CTGF promoter fragments revealed that the −897- to −628-bp fragment contained DEX-responsive positive regulatory elements, which were active in mProx24 but not MCT cells. Long-term DEX treatment resulted in fibronectin deposition in the kidneys of C57B6 but not SJL mice, and this effect was inhibited by co-administration of CTGF anti-sense oligodeoxynucleotides. Thus, glucocorticoid-induced renal fibrogenesis seems to be influenced by genetic background, with the critical DEX-responsive elements in the −897- to −628-bp region of the CTGF promoter.</abstract><cop>Bethesda, MD</cop><pub>Elsevier Inc</pub><pmid>16507889</pmid><doi>10.2353/ajpath.2006.050656</doi><tpages>11</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adolescent Adult Animals Base Sequence Biological and medical sciences Connective Tissue Growth Factor Dexamethasone - pharmacology Epithelial Cells - chemistry Epithelial Cells - drug effects Epithelial Cells - metabolism Female Fibronectins - analysis Fibronectins - metabolism Genes, Reporter Humans Immediate-Early Proteins - analysis Immediate-Early Proteins - biosynthesis Immediate-Early Proteins - genetics Intercellular Signaling Peptides and Proteins - analysis Intercellular Signaling Peptides and Proteins - biosynthesis Intercellular Signaling Peptides and Proteins - genetics Investigative techniques, diagnostic techniques (general aspects) Kidney Tubules - drug effects Kidney Tubules - metabolism Kidney Tubules - pathology Luciferases - analysis Luciferases - genetics Male Medical sciences Mice Mice, Inbred Strains Molecular Sequence Data Nephritis - genetics Nephritis - metabolism Nephritis - pathology Oligodeoxyribonucleotides, Antisense - pharmacology Original Research Paper Pathology. Cytology. Biochemistry. Spectrometry. Miscellaneous investigative techniques Promoter Regions, Genetic RNA, Messenger - analysis RNA, Messenger - metabolism Syndrome Transcription, Genetic - drug effects Up-Regulation |
title | Dexamethasone Induces Connective Tissue Growth Factor Expression in Renal Tubular Epithelial Cells in a Mouse Strain-Specific Manner |
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