Kissin Eugene Y, Lemaire Raphael, Korn Joseph H, Lafyatis Robert
Boston University School of Medicine, Boston, Massachusetts 02118, USA.
Arthritis Rheum. 2002 Nov;46(11):3000-9. doi: 10.1002/art.10621.
Fibrillin, an extracellular matrix protein implicated in dermal fibrosis, is increased in the reticular dermis of systemic sclerosis (SSc) skin. We undertook this study to investigate the hypothesis that transforming growth factor beta (TGFbeta) or other cytokines regulate fibrillin matrix formation by normal and SSc fibroblasts. We further investigated the mechanism of TGFbeta-induced fibrillin fibrillogenesis and its relationship to myofibroblasts.
Fibrillin and fibronectin matrix deposition and alpha-smooth muscle actin expression by fibroblast cultures from normal and SSc skin treated with TGFbeta or other cytokines were analyzed by immunofluorescence. Supernatant and extracellular matrix from normal and SSc fibroblasts treated with or without TGFbeta were evaluated by Western blot and Northern blot for fibrillin protein and messenger RNA (mRNA) expression, respectively.
Immunofluorescence demonstrated increased fibrillin matrix formation by normal and scleroderma fibroblasts after TGFbeta treatment. Other cytokines, including tumor necrosis factor alpha, interleukin-1beta (IL-1beta), IL-4, granulocyte-macrophage colony-stimulating factor, and platelet-derived growth factor, did not affect fibrillin fibrillogenesis. Fibrillin matrix formed in proximity to myofibroblasts and independently of up-regulation of fibronectin matrix or cell number. Western blot analysis of extracellular matrix confirmed increased fibrillin after TGFbeta stimulation of normal or scleroderma fibroblasts. However, TGFbeta did not alter the expression of either soluble fibrillin protein or fibrillin mRNA.
Our data show that TGFbeta induces fibrillin protein incorporation into the extracellular matrix without affecting fibrillin gene expression or protein synthesis, suggesting that fibrillin matrix assembly is regulated extracellularly. TGFbeta might increase fibrillin matrix by activating myofibroblasts. Such TGFbeta-mediated effects could account for the increased fibrillin matrix observed in SSc skin.
原纤维蛋白是一种与皮肤纤维化相关的细胞外基质蛋白,在系统性硬化症(SSc)皮肤的网状真皮中含量增加。我们开展本研究以探讨转化生长因子β(TGFβ)或其他细胞因子调节正常及SSc成纤维细胞中纤连蛋白基质形成的假说。我们进一步研究了TGFβ诱导原纤维蛋白原纤维形成的机制及其与肌成纤维细胞的关系。
通过免疫荧光分析用TGFβ或其他细胞因子处理的正常及SSc皮肤成纤维细胞培养物中原纤维蛋白和纤连蛋白基质沉积以及α平滑肌肌动蛋白表达。分别通过蛋白质印迹法和Northern印迹法评估用或不用TGFβ处理的正常及SSc成纤维细胞的上清液和细胞外基质中的原纤维蛋白和信使核糖核酸(mRNA)表达。
免疫荧光显示TGFβ处理后正常及硬皮病成纤维细胞中原纤维蛋白基质形成增加。其他细胞因子,包括肿瘤坏死因子α、白细胞介素-1β(IL-1β)、IL-4、粒细胞巨噬细胞集落刺激因子和血小板衍生生长因子,均不影响原纤维蛋白原纤维形成。原纤维蛋白基质在肌成纤维细胞附近形成,且与纤连蛋白基质上调或细胞数量无关。细胞外基质的蛋白质印迹分析证实TGFβ刺激正常或硬皮病成纤维细胞后原纤维蛋白增加。然而,TGFβ未改变可溶性原纤维蛋白或原纤维蛋白mRNA的表达。
我们的数据表明,TGFβ诱导原纤维蛋白掺入细胞外基质,而不影响原纤维蛋白基因表达或蛋白质合成,提示原纤维蛋白基质组装在细胞外受到调节。TGFβ可能通过激活肌成纤维细胞增加原纤维蛋白基质。这种TGFβ介导的效应可能解释了在SSc皮肤中观察到的原纤维蛋白基质增加现象。