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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Veröffentlicht in:The American journal of pathology 2006-03, Vol.168 (3), p.737-747
Hauptverfasser: Okada, Hirokazu, Kikuta, Tomohiro, Inoue, Tsutomu, Kanno, Yoshihiko, Ban, Shinichi, Sugaya, Takeshi, Takigawa, Masaharu, Suzuki, Hiromichi
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container_title The American journal of pathology
container_volume 168
creator Okada, Hirokazu
Kikuta, Tomohiro
Inoue, Tsutomu
Kanno, Yoshihiko
Ban, Shinichi
Sugaya, Takeshi
Takigawa, Masaharu
Suzuki, Hiromichi
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. 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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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source MEDLINE; Elsevier ScienceDirect Journals; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central
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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