首页> 外文OA文献 >Transforming Growth Factor-β1 (TGFβ1) Stimulates Connective Tissue Growth Factor (CCN2/CTGF) Expression in Human Gingival Fibroblasts through a RhoA-independent, Rac1/Cdc42-dependent Mechanism: STATINS WITH FORSKOLIN BLOCK TGFβ1-INDUCED CCN2/CTGF EXPRESSION*
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Transforming Growth Factor-β1 (TGFβ1) Stimulates Connective Tissue Growth Factor (CCN2/CTGF) Expression in Human Gingival Fibroblasts through a RhoA-independent, Rac1/Cdc42-dependent Mechanism: STATINS WITH FORSKOLIN BLOCK TGFβ1-INDUCED CCN2/CTGF EXPRESSION*

机译:转化生长因子-β1(TGFβ1)刺激结缔组织 人牙龈成纤维细胞中组织生长因子(CCN2 / CTGF)的表达 通过独立于RhoA,依赖Rac1 / Cdc42的机制:STATINS WITH Forskolin块TGFβ1诱导的CCN2 / CTGF 表达*

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摘要

Regulation of connective tissue growth factor (CCN2/CTGF) in gingival fibroblasts is unique and may provide therapeutic opportunities to treat oral fibrotic diseases. RhoA was previously implicated in mediating the expression of CCN2/CTGF. We now present evidence that Rho family GTPases Rac1 and Cdc42 are the principal mediators of the transforming growth factor-β1 (TGFβ1)-stimulated expression of CCN2/CTGF in primary human gingival fibroblasts. TGFβ1 does not stimulate RhoA activation in gingival fibroblasts, and the overexpression of dominant-negative RhoA does not reduce CCN2/CTGF expression in response to TGFβ1. In contrast, the overexpression of dominant-negative forms of Cdc42 or Rac1 results in a dramatic reduction of CCN2/CTGF protein levels. Lovastatin and a geranylgeranyltransferase inhibitor reduce the TGFβ1-stimulated levels of CCN2/CTGF protein by ∼75 and 100%, respectively. We previously demonstrated that JNK1 phosphorylation by TGFβ1 is also critical for TGFβ1-induced CCN2/CTGF expression, and forskolin partially reduces levels of phosphorylated JNK1. Inhibition of geranylgeranyltransferase has no effect on levels of JNK phosphorylation in response to TGFβ1 suggesting Rho-GTPases act independently of JNK1. The combination of lovastatin and forskolin results in a greater inhibitory effect than each agent alone and reduces CCN2/CTGF mRNA and protein expression by greater than 90%. This novel combination has additive inhibitory effects on the TGFβ1-stimulated expression of CCN2/CTGF in human gingival fibroblasts through the simultaneous disruption of Rho- and JNK1-mediated pathways, respectively. This combination of available therapeutic compounds may therefore be useful in designing treatment strategies for oral fibrotic conditions in which gingival CCN2/CTGF is elevated.
机译:牙龈成纤维细胞中结缔组织生长因子(CCN2 / CTGF)的调节是独特的,可能为治疗口腔纤维化疾病提供治疗机会。 RhoA以前牵涉介导CCN2 / CTGF的表达。我们现在提供证据,证明Rho家族GTPases Rac1和Cdc42是转化生长因子-β1(TGFβ1)刺激的原代人牙龈成纤维细胞CCN2 / CTGF表达的主要介质。 TGFβ1不会刺激牙龈成纤维细胞中的RhoA活化,并且显性阴性RhoA的过表达不会降低对TGFβ1的CCN2 / CTGF表达。相反,显性负性形式的Cdc42或Rac1的过表达导致CCN2 / CTGF蛋白水平的显着降低。洛伐他汀和Geranylgeranyltransferase抑制剂分别降低TGFβ1刺激的CCN2 / CTGF蛋白水平约75%和100%。我们先前证明了TGFβ1磷酸化JNK1对TGFβ1诱导的CCN2 / CTGF表达也很关键,而福司可林部分降低了磷酸化JNK1的水平。抑制香叶基香叶基转移酶对响应TGFβ1的JNK磷酸化水平没有影响,表明Rho-GTPases独立于JNK1起作用。与单独使用每种药物相比,洛伐他汀和毛喉素的结合产生更大的抑制作用,并使CCN2 / CTGF mRNA和蛋白质表达降低90%以上。这种新颖的组合分别通过同时破坏Rho-和JNK1介导的途径,对TGFβ1刺激的人牙龈成纤维细胞中CCN2 / CTGF的表达具有累加抑制作用。因此,可用治疗化合物的这种组合可用于设计其中牙龈CCN2 / CTGF升高的口腔纤维化疾病的治疗策略。

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