Comparative proteomic analysis of extracellular matrix proteins secreted by hypertrophic scar with normal skin fibroblasts

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 基因 体外
作者
Jun Wu,Li Ma,Chengjun Gan,Yong Huang,Ying Wang,Gaoxing Luo
出处
期刊:Burns and trauma [BioMed Central]
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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