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12R-脂氧合酶活性在光损伤的面部角质层中降低。一种新的活性测定法表明其在角质细胞成熟过程中具有关键功能。

12R-lipoxygenase activity is reduced in photodamaged facial stratum corneum. A novel activity assay indicates a key function in corneocyte maturation.

机构信息

UCL School of Pharmacy, London, UK.

DSM Nutritional Products Ltd, Kaiseraugust, Switzerland.

出版信息

Int J Cosmet Sci. 2019 Jun;41(3):274-280. doi: 10.1111/ics.12532. Epub 2019 May 28.

Abstract

BACKGROUND

During the late stage of keratinocyte differentiation, corneocytes gain a strong protein-lipid structure: the corneocyte envelopes (CE), composed of the inner corneocyte protein envelope (CPE) and the outer corneocyte lipid envelope (CLE). The hydrophobicity of CEs depends on the covalent attachment of linoleoyl-acyl-ceramides by transglutaminases (TG). These ceramides are processed by a range of other enzymes, including 12R-lipoxygenase (12R-LOX), before the covalent attachment of the free ω-hydroxyceramides to the CPE surface to form the CLE. The mechanical strength of CE is obtained with the formation of isodipeptide bonds by TG. The increase in hydrophobicity and rigidity leads to CE maturation which supports the integrity and mechanical resistance of the stratum corneum (SC).

OBJECTIVES

The aim of this work was to develop and validate a novel enzyme activity assay for 12R-LOX in tape strippings of photo-exposed (PE) cheek and photo-protected (PP) post-auricular SC of healthy Chinese volunteers (n = 12; age 25 ± 3 years).

RESULTS

A fluorescence-based assay was developed with ethyl linoleic acid as the substrate and a polyclonal antibody against 12R-LOX as an inhibitor. The specificity was shown by the lack of effect by a LOX inhibitor (ML351) and an epidermal-type lipoxygenase 3 (eLOX3) antibody on the acquired 12R-LOX activity. Reduced 12R-LOX activity was observed in the outer compared to the inner SC layers. Moreover, dramatically lower activity was shown in the PE vs. PP samples. Furthermore, the enzyme activity has a positive correlation (r = 0.94 ± 0.03) with CE maturity, in particular hydrophobicity, and a negative correlation (r = -0.96 ± 0.01) with transepidermal water loss (TEWL).

CONCLUSION

This novel enzyme assay revealed a lower 12R-LOX activity in tape strippings from PE cheek for the first time. This finding is in line with less mature CEs and higher TEWL compared to PP post-auricular samples. This study indicates a strong link between 12R-LOX activity and CE maturation and SC integrity.

摘要

背景

在角质形成细胞分化的晚期,角质细胞获得了强大的蛋白脂质结构:角质细胞包膜(CE),由内角质细胞蛋白包膜(CPE)和外角质细胞脂质包膜(CLE)组成。CE 的疏水性取决于转谷氨酰胺酶(TG)通过共价键连接亚油酸酰基神经酰胺。这些神经酰胺在共价连接游离 ω-羟基神经酰胺到 CPE 表面形成 CLE 之前,被一系列其他酶(包括 12R-脂氧合酶(12R-LOX))加工。TG 形成同二肽键可获得 CE 的机械强度。疏水性和刚性的增加导致 CE 成熟,从而支持角质层(SC)的完整性和机械抵抗力。

目的

本研究旨在开发和验证一种新的 12R-LOX 酶活性测定法,用于来自健康中国志愿者(n=12;年龄 25±3 岁)的光暴露(PE)脸颊和光保护(PP)耳后 SC 的胶带剥离物。

结果

用乙基亚油酸作为底物,用针对 12R-LOX 的多克隆抗体作为抑制剂,建立了一种基于荧光的测定法。通过缺乏 LOX 抑制剂(ML351)和表皮型脂氧合酶 3(eLOX3)抗体对获得的 12R-LOX 活性的影响,显示出特异性。在外层 SC 层与内层 SC 层相比,12R-LOX 活性降低。此外,与 PP 样本相比,PE 样本中的活性显著降低。此外,该酶活性与 CE 成熟度(特别是疏水性)呈正相关(r=0.94±0.03),与经表皮水分流失(TEWL)呈负相关(r=-0.96±0.01)。

结论

本研究首次在来自 PE 脸颊的胶带剥离物中发现较低的 12R-LOX 活性。这一发现与与 PP 耳后样本相比,CE 更不成熟和更高的 TEWL 一致。本研究表明 12R-LOX 活性与 CE 成熟度和 SC 完整性之间存在很强的联系。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2ad9/6852689/dca1b54fbfa1/ICS-41-274-g001.jpg

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