Tam Jacqueline Chor Wing, Ko Chun Hay, Zhang Cheng, Wang Hua, Lau Ching Po, Chan Wai Yee, Leung Ping Chung, Fung Kwok Pui, Zhang Jin Fang, Lau Clara Bik San
Institute of Chinese Medicine, The Chinese University of Hong Kong, Shatin, New Territories, Hong Kong; State Key Laboratory of Phytochemistry and Plant Resources in West China, The Chinese University of Hong Kong, Shatin, New Territories, Hong Kong.
Proteomics. 2014 Sep;14(17-18):2089-103. doi: 10.1002/pmic.201300547. Epub 2014 Aug 21.
Endothelial cells are crucially involved in wound healing angiogenesis, restoring blood flow to wound tissues. Our previous study demonstrated that the Chinese 2-herb formula (NF3) possesses significant wound healing effect in diabetic foot ulcer rats with promising in vitro proangiogenic effects on human umbilical vein endothelial cells (HUVEC). Here, we present the comparative global proteome analysis of NF3-treated HUVEC in static or scratch conditions, screening the comprehensive molecular targets in governing the proangiogenic response in wound healing. Our results suggest plasminogen activator inhibitor-1, specifically down-regulated in static condition and Annexin A1 and Annexin A2, up-regulated in scratch condition, as principal proteins responsible for the proangiogenesis in wound healing. We also identified a panel of cytoskeleton regulatory proteins in static and scratch condition, mediating the migratory behavior of NF3-treated HUVEC. The key proteins in static state include myosin regulatory light polypeptide 9, SPAST, tropomyosin (TPM)2, and Vimentin while that in scratch state contained prelamin-A/C, TPM1, TPM2, and Vimentin. In addition, NF3 was shown to regulate transcription and translation, cell-cell interaction, and ROS defense in HUVEC. Proliferation and migration assays further confirmed the identified principal proteins plasminogen activator inhibitor-1 and Annexin A2 which are responsible for NF3-induced proangiogenesis of HUVEC in wound healing. This is the first study on the global proteome expression of NF3-treated HUVEC with the identification of the differences at the molecular level, between static and scratch conditions involved in wound healing angiogenesis.
内皮细胞在伤口愈合血管生成中起关键作用,可恢复伤口组织的血流。我们之前的研究表明,中药二味配方(NF3)对糖尿病足溃疡大鼠具有显著的伤口愈合作用,对人脐静脉内皮细胞(HUVEC)具有有前景的体外促血管生成作用。在此,我们展示了在静态或划痕条件下经NF3处理的HUVEC的比较性全蛋白质组分析,筛选出在伤口愈合中调控促血管生成反应的综合分子靶点。我们的结果表明,纤溶酶原激活物抑制剂-1在静态条件下特异性下调,膜联蛋白A1和膜联蛋白A2在划痕条件下上调,它们是伤口愈合中促血管生成的主要蛋白质。我们还在静态和划痕条件下鉴定出一组细胞骨架调节蛋白,介导经NF3处理的HUVEC的迁移行为。静态状态下的关键蛋白包括肌球蛋白调节轻链多肽9、痉挛蛋白、原肌球蛋白(TPM)2和波形蛋白,而划痕状态下的关键蛋白包括前层粘连蛋白A/C、TPM1、TPM2和波形蛋白。此外,NF3被证明可调节HUVEC中的转录和翻译、细胞间相互作用以及活性氧防御。增殖和迁移试验进一步证实了已鉴定出的主要蛋白质纤溶酶原激活物抑制剂-1和膜联蛋白A2,它们负责NF3诱导的伤口愈合中HUVEC的促血管生成。这是第一项关于经NF3处理的HUVEC全蛋白质组表达的研究,鉴定了在伤口愈合血管生成中静态和划痕条件之间分子水平的差异。