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松属素在人角质形成细胞中发挥再生活性的分子靶点

Molecular Targets of Pinocembrin Underlying Its Regenerative Activities in Human Keratinocytes.

作者信息

Ruttanapattanakul Jirapak, Wikan Nitwara, Potikanond Saranyapin, Nimlamool Wutigri

机构信息

Department of Pharmacology, Faculty of Medicine, Chiang Mai University, Chiang Mai 50200, Thailand.

Graduate School, Chiang Mai University, Chiang Mai 50200, Thailand.

出版信息

Pharmaceuticals (Basel). 2022 Jul 31;15(8):954. doi: 10.3390/ph15080954.

Abstract

Pinocembrin is one of the well-known compounds in the group of flavonoids. The pharmacological activities of pinocembrin in association with wound-healing activities have been reported. However, its effects on the aspect of cellular interaction underlying growth and survival are still unidentified in human keratinocytes. Our previous study reported that potently stimulated survival and proliferation of a human keratinocyte cell line (HaCaT). On the basis that pinocembrin is revealed to be one of the major constituents of this plant, we aimed to define the survival- and proliferation-enhancing effects of this compound at the cellular level. Results from the current study confirmed that pinocembrin induced an increase in HaCaT cell number. At the signaling perspective, we identified that pinocembrin significantly triggered ERK1/2 and Akt activation. The stimulating effects of pinocembrin were clearly inhibited by MEK and PI3K inhibitors authenticating that proliferation- and survival-promoting activities of pinocembrin were mainly acted on these two signaling cascades. Altogether, we successfully identified that pinocembrin functions to induce keratinocyte proliferation and survival, at least by provoking MAPK and PI3K pathways. Our study encourages the fact that pinocembrin is one of the interesting natural flavonoid compounds to be developed as a wound closure-promoting agent.

摘要

松属素是黄酮类化合物中一种广为人知的化合物。松属素与伤口愈合活性相关的药理活性已有报道。然而,其在人角质形成细胞中对生长和存活潜在的细胞相互作用方面的影响仍不明确。我们之前的研究报道,[此处原文缺失信息]能有效刺激人角质形成细胞系(HaCaT)的存活和增殖。鉴于松属素被发现是这种植物的主要成分之一,我们旨在在细胞水平上确定该化合物增强存活和增殖的作用。当前研究结果证实,松属素可诱导HaCaT细胞数量增加。从信号转导角度来看,我们发现松属素能显著触发ERK1/2和Akt的激活。MEK和PI3K抑制剂可明显抑制松属素的刺激作用,这证实了松属素促进增殖和存活的活性主要作用于这两个信号级联反应。总之,我们成功确定松属素至少通过激活MAPK和PI3K途径发挥诱导角质形成细胞增殖和存活的作用。我们的研究支持了松属素是一种有开发潜力的、可作为促进伤口愈合药物的天然黄酮类化合物这一观点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f5e/9415973/07be941d6695/pharmaceuticals-15-00954-g001.jpg

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