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表皮分化过程中透明质酸代谢增强被维生素 C 抑制。

Hyaluronan metabolism enhanced during epidermal differentiation is suppressed by vitamin C.

机构信息

Institute of Biomedicine/Anatomy, University of Eastern Finland, P.O. Box 1627, FI-70211, Kuopio, Finland.

Dentistry, University of Eastern Finland, P.O. Box 1627, FI-70211, Kuopio, Finland.

出版信息

Br J Dermatol. 2018 Sep;179(3):651-661. doi: 10.1111/bjd.16423. Epub 2018 May 15.

Abstract

BACKGROUND

Hyaluronan is a large, linear glycosaminoglycan present throughout the narrow extracellular space of the vital epidermis. Increased hyaluronan metabolism takes place in epidermal hypertrophy, wound healing and cancer. Hyaluronan is produced by hyaluronan synthases and catabolized by hyaluronidases, reactive oxygen species and KIAA1199.

OBJECTIVES

To investigate the changes in hyaluronan metabolism during epidermal stratification and maturation, and the impact of vitamin C on these events.

METHODS

Hyaluronan synthesis and expression of the hyaluronan-related genes were analysed during epidermal maturation from a simple epithelium to a fully differentiated epidermis in organotypic cultures of rat epidermal keratinocytes using quantitative reverse transcriptase polymerase chain reaction, immunostaining and Western blotting, in the presence and absence of vitamin C.

RESULTS

With epidermal stratification, both the production and the degradation of hyaluronan were enhanced, resulting in an increase of hyaluronan fragments of various sizes. While the mRNA levels of Has3 and KIAA1199 remained stable during the maturation, Has1, Has2 and Hyal2 showed a transient upregulation during stratification, Hyal1 transcription remained permanently increased and transcription of the hyaluronan receptor, Cd44, decreased. At maturation, vitamin C downregulated Has2, Hyal2 and Cd44, whereas it increased high-molecular-mass hyaluronan in the epidermis, and reduced small fragments in the medium, suggesting stabilization of epidermal hyaluronan.

CONCLUSIONS

Epidermal stratification and maturation is associated with enhanced hyaluronan turnover, and release of large amounts of hyaluronan fragments. The high turnover is suppressed by vitamin C, which is suggested to enhance normal epidermal differentiation in part through its effect on hyaluronan.

摘要

背景

透明质酸是一种大的线性糖胺聚糖,存在于生命表皮的狭窄细胞外空间中。表皮肥大、伤口愈合和癌症中会发生透明质酸代谢增加。透明质酸由透明质酸合酶产生,并被透明质酸酶、活性氧和 KIAA1199 分解代谢。

目的

研究表皮分层和成熟过程中透明质酸代谢的变化,以及维生素 C 对这些事件的影响。

方法

在大鼠表皮角质形成细胞的器官型培养中,通过定量逆转录聚合酶链反应、免疫染色和 Western blot 分析,在存在和不存在维生素 C 的情况下,分析从简单上皮到完全分化的表皮的表皮成熟过程中透明质酸的合成和透明质酸相关基因的表达。

结果

随着表皮分层,透明质酸的产生和降解都增强了,导致各种大小的透明质酸片段增加。虽然 Has3 和 KIAA1199 的 mRNA 水平在成熟过程中保持稳定,但 Has1、Has2 和 Hyal2 在分层过程中表现出短暂的上调,Hyal1 的转录永久增加,透明质酸受体 Cd44 的转录减少。在成熟时,维生素 C 下调 Has2、Hyal2 和 Cd44,而在表皮中增加高分子质量透明质酸,减少培养基中的小片段,表明表皮透明质酸稳定。

结论

表皮分层和成熟与增强的透明质酸周转率和大量透明质酸片段的释放有关。高周转率被维生素 C 抑制,维生素 C 通过其对透明质酸的作用,部分增强正常表皮分化。

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