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弥漫性皮肤系统性硬皮病的皮肤组织和细胞纤维连接蛋白-1的表达。

Dermal tissue and cellular expression of fibrillin-1 in diffuse cutaneous systemic sclerosis.

机构信息

Université Paris Descartes, Rhumatologie A, Hôpital Cochin, AP-HP, Paris, France.

出版信息

Rheumatology (Oxford). 2010 Apr;49(4):657-61. doi: 10.1093/rheumatology/kep433. Epub 2010 Jan 16.

DOI:10.1093/rheumatology/kep433
PMID:20081226
Abstract

OBJECTIVE

To assess dermal expression and fibroblast production of fibrillin-1 (FBN-1) in SSc.

METHODS

In vivo analysis of microfibrillar network was performed using EM from affected and unaffected skin biopsy specimens of dcSSc patients (n = 5) compared with healthy controls (n = 2). FBN-1 matrix deposition and organization by dermal fibroblast cultures from dcSSc (n = 6), healthy (n = 5) and Marfan (n = 4) controls was analysed in vitro by IF with or without TGF-beta activation. Finally, production of FBN-1 by cultured dermal fibroblasts was evaluated by western blot (WB) and real-time PCR.

RESULTS

We observed a striking decrease of tissue microfibrillar network in the dermis of SSc patients compared with healthy controls affecting both clinically involved and uninvolved skin. In cultures, SSc dermal fibroblasts displayed no apparent in vitro alteration of synthesis, secretion and organization of microfibril network. The WB and real-time PCR analyses showed similar FBN-1 amounts in matrix and FBN1 gene expression in SSc and healthy controls.

CONCLUSIONS

We observed a striking decrease of in vivo microfibrillar network in clinically affected and unaffected skin in early dcSSc patients. This does not relate to an inability of SSc dermal fibroblasts to produce, secrete and organize microfibrils in vitro. Therefore, the disturbances of microfibrils in SSc may be a secondary event to matrix remodelling that occurs in this disease.

摘要

目的

评估硬皮病中纤维连接蛋白-1(FBN-1)的皮肤表达和成纤维细胞产生情况。

方法

通过 EM 对 dcSSc 患者(n=5)与健康对照者(n=2)的皮肤活检标本进行体内分析,比较受影响和未受影响的皮肤的微纤维网络。通过 IF 分析来自 dcSSc(n=6)、健康(n=5)和马凡氏综合征(n=4)对照者的成纤维细胞培养物的 FBN-1 基质沉积和组织情况,是否有 TGF-β激活。最后,通过 WB 和实时 PCR 评估培养的真皮成纤维细胞产生 FBN-1 的情况。

结果

与健康对照者相比,我们观察到 SSc 患者皮肤真皮中的组织微纤维网络明显减少,影响到有临床症状和无症状的皮肤。在培养物中,SSc 真皮成纤维细胞的微纤维网络合成、分泌和组织体外无明显变化。WB 和实时 PCR 分析显示 SSc 和健康对照者基质中 FBN-1 含量和 FBN1 基因表达相似。

结论

我们观察到早期 dcSSc 患者临床受影响和不受影响的皮肤中微纤维网络明显减少。这与 SSc 真皮成纤维细胞在体外产生、分泌和组织微纤维的能力无关。因此,SSc 中微纤维的紊乱可能是发生在这种疾病中的基质重塑的继发事件。

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