大黄素和芦荟大黄素:通过MAP激酶途径调节皮肤细胞迁移并影响秀丽隐杆线虫耐热性的两种潜在分子

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS
Aysenur Gunaydin-Akyildiz, Rabia Sare Yanikoglu, Meltem Gulec, Gulbahar Ozge Alim-Toraman, Ebru Didem Kuran, Sezen Atasoy, Abdullah Olgun, Gulacti Topcu
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引用次数: 0

摘要

背景:大黄素和芦荟大黄素是两种对伤口愈合有积极作用的蒽醌类药物。然而,它们对伤口愈合的作用机制尚不完全清楚。MAP激酶家族在伤口愈合中发挥积极作用,是一个具有良好特征的丝氨酸/苏氨酸激酶大家族,调节细胞增殖、肿瘤发生、分化和炎症等过程。本研究的目的是比较阐明大黄素和芦荟大黄素的作用机制,这是潜在的伤口愈合药物。方法:以人皮肤成纤维细胞(CCD-1079Sk)为实验对象,研究大黄素和芦荟大黄素对细胞活力和细胞迁移的影响机制。研究了MAP激酶(JNK、P38、ERK)在皮肤成纤维细胞中的基因表达水平,并进行了分子对接研究,分析了它们的相互作用潜力。此外,还研究了这些分子对秀丽隐杆线虫寿命的影响。结果:大黄素和芦荟大黄素抑制细胞ATP含量呈浓度依赖关系,低浓度处理组加速细胞迁移,高浓度处理组抑制细胞迁移。JNK和P38在低浓度下表达上调,在高浓度下表达下调。分子对接研究给出了很高的对接分数,表明它们与JNK和P38的相互作用潜力。75µM大黄素处理后秀丽隐杆线虫的热应激寿命延长,150µM芦荟大黄素处理后线虫的热应激寿命明显缩短。结论:芦荟大黄素对秀丽隐杆线虫健康成纤维皮肤细胞的细胞活力、细胞迁移、MAP激酶基因表达水平和寿命有更大的影响。本研究揭示了大黄素和芦荟大黄素在创面愈合过程中的功能作用及相互作用的生物学因素,为缩短创面护理时间提供了可能的治疗选择。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Emodin and aloe-emodin, two potential molecules in regulating cell migration of skin cells through the MAP kinase pathway and affecting Caenorhabditis elegans thermotolerance.

Emodin and aloe-emodin, two potential molecules in regulating cell migration of skin cells through the MAP kinase pathway and affecting Caenorhabditis elegans thermotolerance.

Emodin and aloe-emodin, two potential molecules in regulating cell migration of skin cells through the MAP kinase pathway and affecting Caenorhabditis elegans thermotolerance.

Emodin and aloe-emodin, two potential molecules in regulating cell migration of skin cells through the MAP kinase pathway and affecting Caenorhabditis elegans thermotolerance.

Background: Emodin and aloe-emodin are two anthraquinones having positive effects in wound healing. However, their mechanism of action of wound healing is not fully understood. The MAP kinase family, which plays an active role in wound healing, is a well-characterized large family of serine/threonine kinases and regulates processes such as proliferation, oncogenesis, differentiation, and inflammation in the cell. The aim of this study is to comparatively elucidate the mechanisms of action of emodin and aloe-emodin, which are potential agents in wound healing.

Methods: The mechanism of the effects of emodin and aloe-emodin on cell viability and cell migration was examined using the human skin fibroblast (CCD-1079Sk) cell line. The gene expression levels of the MAP kinases (JNK, P38, ERK) in the skin fibroblast cells along with a molecular docking study analyzing their interaction potential were evaluated. Furthermore, the molecules' effects on the lifespan of Caenorhabditis elegans were studied.

Results: Emodin and aloe-emodin inhibited the ATP content of the cells in a concentration dependent manner and accelerated cell migration at the lower concentrations while inhibiting cell migration in the higher concentration treatment groups. The expressions of JNK and P38 were upregulated at the low concentrations and downregulated at the higher concentrations. The molecular docking studies of the molecules gave high docking scores indicating their interaction potential with JNK and P38. C. elegans lifespan under heat stress was observed longer after 75 µM emodin and was significantly reduced after 150 µM aloe-emodin treatment.

Conclusion: Aloe-emodin was found to be more potent on cell viability, cell migration, gene expression levels of the MAP kinases in healthy fibroblastic skin cells, and on the lifespan of C. elegans. This study reveals the functional effects and the biological factors that interact in the wound healing process of emodin and aloe-emodin, and give a possible treatment alternative to shorten the duration of wound care.

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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
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