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使用STRING数据库分析真皮乳头细胞相互作用组,以评估长春花生物碱药物秋水仙碱对离体毛发生长的抑制作用。

Analysis of dermal papilla cell interactome using STRING database to profile the ex vivo hair growth inhibition effect of a vinca alkaloid drug, colchicine.

作者信息

Hsia Ching-Wu, Ho Ming-Yi, Shui Hao-Ai, Tsai Chong-Bin, Tseng Min-Jen

机构信息

Institute of Molecular Biology and Department of Life Science, National Chung Cheng University, Chia-yi 621, Taiwan.

Institute of Stem Cell and Translational Cancer Research, Chang Gung Memorial Hospital, Taoyuan 333, Taiwan.

出版信息

Int J Mol Sci. 2015 Feb 5;16(2):3579-98. doi: 10.3390/ijms16023579.

Abstract

Dermal papillae (DPs) control the formation of hair shafts. In clinical settings, colchicine (CLC) induces patients' hair shedding. Compared to the control, the ex vivo hair fiber elongation of organ cultured vibrissa hair follicles (HFs) declined significantly after seven days of CLC treatment. The cultured DP cells (DPCs) were used as the experimental model to study the influence of CLC on the protein dynamics of DPs. CLC could alter the morphology and down-regulate the expression of alkaline phosphatase (ALP), the marker of DPC activity, and induce IκBα phosphorylation of DPCs. The proteomic results showed that CLC modulated the expression patterns (fold>2) of 24 identified proteins, seven down-regulated and 17 up-regulated. Most of these proteins were presumably associated with protein turnover, metabolism, structure and signal transduction. Protein-protein interactions (PPI) among these proteins, established by Search Tool for the Retrieval of Interacting Genes/Proteins (STRING) database, revealed that they participate in protein metabolic process, translation, and energy production. Furthermore, ubiquitin C (UbC) was predicted to be the controlling hub, suggesting the involvement of ubiquitin-proteasome system in modulating the pathogenic effect of CLC on DPC.

摘要

真皮乳头(DPs)控制毛干的形成。在临床环境中,秋水仙碱(CLC)会导致患者脱发。与对照组相比,经CLC处理7天后,器官培养的触须毛囊(HFs)的离体毛纤维伸长显著下降。培养的DP细胞(DPCs)被用作实验模型,以研究CLC对DPs蛋白质动力学的影响。CLC可改变DPCs的形态,下调DPC活性标志物碱性磷酸酶(ALP)的表达,并诱导DPCs的IκBα磷酸化。蛋白质组学结果表明,CLC调节了24种已鉴定蛋白质的表达模式(倍数>2),其中7种下调,17种上调。这些蛋白质中的大多数可能与蛋白质周转、代谢、结构和信号转导有关。通过搜索相互作用基因/蛋白质检索工具(STRING)数据库建立的这些蛋白质之间的蛋白质-蛋白质相互作用(PPI)表明,它们参与蛋白质代谢过程、翻译和能量产生。此外,泛素C(UbC)被预测为控制枢纽,表明泛素-蛋白酶体系统参与调节CLC对DPC的致病作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7250/4346914/073d8f1689f2/ijms-16-03579-g001.jpg

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