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[微波加热对慢性肢体淋巴水肿皮肤纤维化的调节作用]

[Microwave heating modulation of skin fibrosis in chronic extremity lymphedema].

作者信息

Cao W, Zhang D, Gan J

机构信息

Department of Plastic and Reconstructive Surgery, Ninth People's Hospital, Shanghai 200011, China.

出版信息

Zhonghua Zheng Xing Wai Ke Za Zhi. 2000 Nov;16(6):354-6.

Abstract

OBJECTIVE

To observe the effects of microwave heating on skin fibrosis in chronic extremity lymphedema.

METHODS

Skin specimens from 8 cases of chronic limb lymphedema were tested by in situ hybridization (ISH) combined with avidin-biotin peroxidase (ABC) immunohistochemistry for detection of TGF-beta, procollagen I, procollagen III mRNAs and corresponding peptides expressions.

RESULTS

It was discovered that expressions of TGF-beta 1 peptide were located at the spinous and granular layer of the epidermal cells with a great amount of dermal collagen I, III formation in accordance with high expressions of TGF-beta, procollagen I, procollagen III mRNAs in the dermal and subcutaneous tissue fibroblasts. After microwave heating treatment, the epidermal expression of TGF-beta 1 and relative TGF-beta, procollagen I, procollagen III mRNAs expressions in dermal fibroblasts were greatly reduced. The smaller calibre of collagen fibers after microwave heating was also observed.

CONCLUSIONS

It is indicated that fibrosis in lymphedema is resulted from overexpressions of relevant genes like TGF-beta and subsequent extracellular matrixes (ECM) syntheses and deposition. Microwave heating can reduce fibroblast expressions of TGF-beta, procollagen I, procollagen III mRNAs as well as TGF-beta peptide synthesis, inhibiting ECM syntheses and deposition and finally reverse the skin fibrosis process.

摘要

目的

观察微波加热对慢性肢体淋巴水肿皮肤纤维化的影响。

方法

采用原位杂交(ISH)结合抗生物素蛋白-生物素过氧化物酶(ABC)免疫组化法,检测8例慢性肢体淋巴水肿患者的皮肤标本中转化生长因子-β(TGF-β)、I型前胶原、III型前胶原mRNA及其相应肽的表达。

结果

发现TGF-β1肽的表达位于表皮细胞的棘层和颗粒层,真皮中大量I、III型胶原形成,同时真皮和皮下组织成纤维细胞中TGF-β、I型前胶原、III型前胶原mRNA高表达。微波加热治疗后,TGF-β1的表皮表达及真皮成纤维细胞中相关TGF-β、I型前胶原、III型前胶原mRNA表达均显著降低。还观察到微波加热后胶原纤维直径变小。

结论

表明淋巴水肿中的纤维化是由TGF-β等相关基因过度表达以及随后细胞外基质(ECM)合成和沉积所致。微波加热可降低成纤维细胞中TGF-β、I型前胶原、III型前胶原mRNA的表达以及TGF-β肽的合成,抑制ECM合成和沉积,最终逆转皮肤纤维化进程。

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