α-酮戊二酸二甲酯能促进 HaCaT 细胞中胶原蛋白的合成并抑制金属蛋白酶。

IF 3 3区 医学 Q2 PHARMACOLOGY & PHARMACY
Biomolecules & Therapeutics Pub Date : 2024-03-01 Epub Date: 2024-02-01 DOI:10.4062/biomolther.2023.131
Bo-Yeong Yu, Da-Hae Eom, Hyun Woo Kim, Yong-Joo Jeong, Young-Sam Keum
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引用次数: 0

摘要

我们观察到,用α-酮戊二酸二甲酯(DMK)处理后,HaCaT 细胞内α-酮戊二酸的增加量明显高于α-酮戊二酸的增加量。DMK 还能提高细胞内 4-羟脯氨酸的水平,促进 HaCaT 细胞胶原蛋白的生成。此外,DMK 还能减少胶原酶和弹性蛋白酶的产生,并通过转录抑制作用下调某些基质金属蛋白酶(MMPs)的表达,如 MMP-1、MMP-9、MMP-10 和 MMP-12。DMK对MMPs的抑制作用是通过抑制IL-1信号级联,从而导致ERK1/2磷酸化和AP-1转录激活的减弱来实现的。我们的研究结果表明,α-酮戊二酸的烷基化衍生物 DMK 通过影响 HaCaT 细胞中的 IL-1 级联和 AP-1 转激活,提高了 4-羟脯氨酸的水平,促进了胶原蛋白的生成,并抑制了特定 MMPs 的表达。结果表明,DMK 可作为一种抗皱成分。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Dimethyl α-Ketoglutarate Promotes the Synthesis of Collagen and Inhibits Metalloproteinases in HaCaT Cells.

We observed that treatment with dimethyl α-ketoglutarate (DMK) increased the amount of intracellular α-ketoglutarate significantly more than that of α-ketoglutarate in HaCaT cells. DMK also increased the level of intracellular 4-hydroxyproline and promoted the production of collagen in HaCaT cells. In addition, DMK decreased the production of collagenase and elastase and down-regulated the expression of selected matrix metalloproteinases (MMPs), such as MMP-1, MMP-9, MMP-10, and MMP-12, via transcriptional inhibition. The inhibition of MMPs by DMK was mediated by the suppression of the IL-1 signaling cascade, leading to the attenuation of ERK1/2 phosphorylation and AP-1 transactivation. Our study results illustrate that DMK, an alkylated derivative of α-ketoglutarate, increased the level of 4-hydroxyproline, promoted the production of collagen, and inhibited the expression of selected MMPs by affecting the IL-1 cascade and AP-1 transactivation in HaCaT cells. The results suggest that DMK might be useful as an anti-wrinkle ingredient.

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来源期刊
CiteScore
6.60
自引率
8.10%
发文量
72
审稿时长
6-12 weeks
期刊介绍: Biomolecules & Therapeutics (Biomolecules & Therapeutics) (Print ISSN 1976-9148, Online ISSN 2005-4483) is an international, peer-reviewed, open access journal that covers pharmacological and toxicological fields related to bioactive molecules and therapeutics. It was launched in 1993 as "The Journal of Applied Pharmacology (ISSN 1225-6110)", and renamed "Biomolecules & Therapeutics" (Biomol Ther: abbreviated form) in 2008 (Volume 16, No. 1). It is published bimonthly in January, March, May, July, September and November. All manuscripts should be creative, informative, and contribute to the development of new drugs. Articles in the following categories are published: review articles and research articles.
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