多糖
卢米坎
纤维连接蛋白
细胞外基质
增生性瘢痕
伤口愈合
化学
污渍
Tenascin公司
免疫印迹
细胞生物学
疤痕
瘢痕疙瘩
纤维发生
分子生物学
生物化学
生物
病理
蛋白多糖
免疫学
医学
解剖
体外
基因
作者
Jun Wu,Li Ma,Chengjun Gan,Yong Huang,Ying Wang,Gaoxing Luo
出处
期刊:Burns and trauma
[BioMed Central]
日期:2014-01-01
卷期号:2 (2): 76-76
被引量:26
标识
DOI:10.4103/2321-3868.130191
摘要
The formation of hypertrophic scars (HSs) is a fibroproliferative disorder of abnormal wound healing. HSs usually characterize excessive proliferation of fibroblasts, abnormal deposition of extracellular matrix (ECM) during wound healing, associated with cosmetic, functional, and psychological problems. Owing to the role of ECM proteins in scar formation, we comparatively analyzed matrix proteins secreted by normal skin fibroblasts (NSFs) and HS fibroblasts (HSFs). The acetone-extracted secreted proteins were separated by sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE), and identified by mass spectrometry (MS). Based on Go annotation of MS data, the profiling of ECM proteins was established and scar-related proteins have been screened out. The functions of several ECM proteins identified by MS have been discussed, such as collagens I, VI, XII, fibronectin, decorin, lumican, and protein procollagen C endopeptidase enhancer 1 (PCPE-1). Among them, the MS result of PCPE-1 was supported by Western blotting that PCPE-1 from HSFs were significantly upregulated than that from NSFs. It is suggested that PCPE-1 could be a potential target for scar treatment. The exploration of scar related proteins may provide new perspectives on understanding the mechanism of scar formation and open a new way to scar treatment and prevention.
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