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Ha-Ras stabilization mediates pro-fibrotic signals in dermal fibroblasts

机译:Ha-Ras稳定介导真皮成纤维细胞中促纤维化信号

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摘要

BackgroundScleroderma (systemic sclerosis; SSc) is a clinically heterogeneous and often lethal acquired disorder of the connective tissue that is characterized by vascular, immune/inflammatory and fibrotic manifestations. Tissue fibrosis is the main cause of morbidity and mortality in SSc and an unmet medical challenge, mostly because of our limited understanding of the molecular factors and signalling events that trigger and sustain disease progression. Recent evidence has correlated skin fibrosis in SSc with stabilization of proto-oncogene Ha-Ras secondary to auto-antibody stimulation of reactive oxygen species production. The goal of the present study was to explore the molecular connection between Ha-Ras stabilization and collagen I production, the main read-out of fibrogenesis, in a primary dermal fibroblast culture system that replicates the early stages of disease progression in SSc.
机译:背景硬皮病(系统性硬化症; SSc)是结缔组织的临床异质性疾病,通常是致死性获得性疾病,其特征是血管,免疫/炎症和纤维化表现。组织纤维化是SSc发病率和死亡率的主要原因,也是医疗挑战尚未解决的主要原因,这主要是因为我们对触发和维持疾病进展的分子因素和信号事件的了解有限。最近的证据已将SSc中的皮肤纤维化与继发于自身抗体刺激活性氧产生的原癌基因Ha-Ras的稳定化相关。本研究的目的是探索在原代皮肤成纤维细胞培养系统中Ha-Ras稳定与胶原I生成之间的分子联系,胶原I生成是纤维形成的主要读数,该系统复制SSc中疾病进展的早期阶段。

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