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系统性硬化症患者皮肤成纤维细胞的寿命

Life span of skin fibroblasts in patients with systemic sclerosis.

作者信息

Ohtsuka T

机构信息

Department of Dermatology, Dokkyo University School of Medicine, Tochigi, Japan.

出版信息

Dermatology. 1998;196(2):204-7. doi: 10.1159/000017899.

DOI:10.1159/000017899
PMID:9568408
Abstract

BACKGROUND

It remains unknown whether the life span of systemic sclerosis (SSc) skin fibroblasts (FB) and that of normals are the same or not, though SSc skin FB have been shown to present abnormalities such as elevated collagen synthesis.

OBJECTIVE

To find out whether the life span of SSc skin FB and that of normals are the same or not.

METHODS

Cell generation and colony-forming efficiency were calculated in 10 normal and 7 SSc FB, and total life spans were studied.

RESULTS

Colony-forming efficiency decreased from 30 to 5% until the cells reached senescence. The cell generations of normal and SSc FB showed no significant difference.

CONCLUSION

SSc FB is senescent and may indicate that the senescence of SSc FB is independent of its abnormal features.

摘要

背景

尽管系统性硬化症(SSc)皮肤成纤维细胞(FB)已被证明存在诸如胶原蛋白合成增加等异常情况,但其寿命与正常人皮肤成纤维细胞是否相同仍不清楚。

目的

探究SSc皮肤FB的寿命与正常人的是否相同。

方法

计算10例正常皮肤FB和7例SSc皮肤FB的细胞传代和集落形成效率,并研究其总寿命。

结果

在细胞达到衰老之前,集落形成效率从30%降至5%。正常皮肤FB和SSc皮肤FB的细胞传代没有显著差异。

结论

SSc皮肤FB发生衰老,这可能表明SSc皮肤FB的衰老与其异常特征无关。

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Life span of skin fibroblasts in patients with systemic sclerosis.系统性硬化症患者皮肤成纤维细胞的寿命
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Systemic sclerosis fibroblasts inhibit in vitro angiogenesis by MMP-12-dependent cleavage of the endothelial cell urokinase receptor.系统性硬化症成纤维细胞通过基质金属蛋白酶-12依赖性切割内皮细胞尿激酶受体来抑制体外血管生成。
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Monocyte chemoattractant protein 3 as a mediator of fibrosis: Overexpression in systemic sclerosis and the type 1 tight-skin mouse.单核细胞趋化蛋白3作为纤维化的介质:在系统性硬化症和1型紧皮小鼠中的过表达。
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Collagen turnover is diminished by different clones of skin fibroblasts from early- but not late-stage systemic sclerosis.来自早期而非晚期系统性硬化症的不同皮肤成纤维细胞克隆会减少胶原蛋白周转。
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[Role of PDGF-A/PDGFR-α in proliferation and transdifferentiation of fibroblasts from skin lesions of patients with systemic sclerosis].[血小板衍生生长因子-A/血小板衍生生长因子受体-α在系统性硬化症患者皮肤病变成纤维细胞增殖和转分化中的作用]
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Circulating γ/δ T cells in systemic sclerosis exhibit activated phenotype and enhance gene expression of proalpha2(I) collagen of fibroblasts.循环 γ/δ T 细胞在系统性硬化症中表现出激活表型,并增强成纤维细胞的 proalpha2(I) 胶原基因表达。
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