Analysis of Dermal Papilla Cell Interactome Using STRING Database to Profile the ex Vivo Hair Growth Inhibition Effect of a Vinca Alkaloid Drug, Colchicine

被引:26
作者
Hsia, Ching-Wu [1 ,2 ]
Ho, Ming-Yi [3 ]
Shui, Hao-Ai [4 ]
Tsai, Chong-Bin [1 ,2 ,5 ]
Tseng, Min-Jen [1 ,2 ]
机构
[1] Natl Chung Cheng Univ, Inst Mol Biol, Chiayi 621, Taiwan
[2] Natl Chung Cheng Univ, Dept Life Sci, Chiayi 621, Taiwan
[3] Chang Gung Mem Hosp, Inst Stem Cell & Translat Canc Res, Taoyuan 333, Taiwan
[4] Natl Def Med Ctr, Grad Inst Med Sci, Taipei 114, Taiwan
[5] Chia Yi Christian Hosp, Dept Ophthalmol, Chiayi 600, Taiwan
关键词
NF-KAPPA-B; INTERACTION NETWORKS; PROTEOMIC ANALYSIS; INDUCED ALOPECIA; GENE-EXPRESSION; DOWN-REGULATION; DIVERSE ROLES; STEM-CELLS; FOLLICLE; PROTEIN;
D O I
10.3390/ijms16023579
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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 I kappa B alpha 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.
引用
收藏
页码:3579 / 3598
页数:20
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