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Dexamethasone Induces Connective Tissue Growth Factor Expression in Renal Tubular Epithelial Cells in a Mouse Strain-Specific Manner

机译:地塞米松以小鼠株特异性方式诱导肾小管上皮细胞中结缔组织生长因子的表达

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摘要

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.
机译:结缔组织生长因子(CTGF)是转化生长因子-β1的下游介体,介导肾小球系膜细胞/成纤维细胞增殖和细胞外基质产生。在这里,我们显示糖皮质激素治疗后,来自肾功能不全综合征患者的肾小管上皮细胞产生了CTGF。此外,糖皮质激素地塞米松(DEX)增加了C57B6小鼠肾脏的CTGF mRNA水平,但不增加SJL小鼠的肾脏,并在F1(C57B6×SJL)小鼠肾脏中产生了中等的CTGF mRNA水平,介于亲本菌株水平之间。 DEX还通过转录上调CTGF mRNA的表达,提高了C57B6(mProx24)而非SJL(MCT)小鼠来源的培养的肾小管上皮细胞的CTGF mRNA水平。使用带有CTGF启动子片段的荧光素酶报道基因构建体进行的瞬时转染实验表明,-897-至-628-bp片段包含DEX响应阳性调控元件,该元件在mProx24中具有活性,但在MCT细胞中不活跃。长期的DEX治疗会导致纤连蛋白在C57B6的肾脏中沉积,但不会在SJL小鼠的肾脏中沉积,这种作用被CTGF反义寡聚脱氧核苷酸的共同给药所抑制。因此,糖皮质激素诱导的肾纤维化似乎受到遗传背景的影响,其关键的DEX反应元件位于CTGF启动子的-897-至-628-bp区域。

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