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血管紧张素受体在人类皮肤伤口愈合中的差异表达。

Differential expression of angiotensin receptors in human cutaneous wound healing.

作者信息

Steckelings U M, Henz B M, Wiehstutz S, Unger T, Artuc M

机构信息

Centre for Cardiovascular Research, Institute for Pharmacology and Toxicology, Charité-Universitätsmedizin Berlin, Hessische Strasse 3-4, 10115 Berlin, Germany.

出版信息

Br J Dermatol. 2005 Nov;153(5):887-93. doi: 10.1111/j.1365-2133.2005.06806.x.

Abstract

BACKGROUND

Angiotensin AT1 and AT2 receptors are expressed in human skin. Furthermore, AT2 receptors have been reported to be upregulated during tissue repair and remodelling in various noncutaneous human tissues.

OBJECTIVES

Detection of alterations in angiotensin II receptor expression during wound healing in human skin.

METHODS

Three models were employed. (i) Primary human keratinocytes were razor scraped in culture flasks and alterations in the expression of angiotensin receptor mRNA determined by semiquantitative reverse transcription-polymerase chain reaction for 1-12 h thereafter. (ii) Early wound healing (48 h after cutting) was studied in punch biopsies from human skin ex vivo by means of immunohistochemical staining using polyclonal antibodies against the AT1 or AT2 receptor. (iii) In vivo wound healing was studied in sections of human cutaneous scars by immunohistochemistry to determine receptor expression early (2 days) and late (2 weeks-3 months) after surgery.

RESULTS

In all experimental settings, an upregulation of both receptor subtypes was noticed after wounding. Immunohistochemically stained skin sections showed a stronger expression of AT2 than of AT1 receptors within the area of scarring. Enhanced receptor expression was detectable as early as 24 h after injury and lasted for up to 3 months.

CONCLUSIONS

From these data, we conclude that angiotensin AT1 and AT2 receptors are upregulated in human cutaneous wounds, giving further support to the concept that angiotensin II plays a role even at an early stage during cutaneous wound healing.

摘要

背景

血管紧张素AT1和AT2受体在人类皮肤中表达。此外,据报道,在各种非皮肤人类组织的组织修复和重塑过程中,AT2受体表达上调。

目的

检测人类皮肤伤口愈合过程中血管紧张素II受体表达的变化。

方法

采用了三种模型。(i)在培养瓶中用剃须刀刮擦原代人角质形成细胞,然后在1-12小时内通过半定量逆转录-聚合酶链反应测定血管紧张素受体mRNA表达的变化。(ii)通过使用抗AT1或AT2受体的多克隆抗体进行免疫组织化学染色,对取自人类皮肤的离体打孔活检组织进行早期伤口愈合(切割后48小时)研究。(iii)通过免疫组织化学对人类皮肤瘢痕切片进行体内伤口愈合研究,以确定手术后早期(2天)和晚期(2周-3个月)的受体表达。

结果

在所有实验设置中,受伤后两种受体亚型均上调。免疫组织化学染色的皮肤切片显示,在瘢痕形成区域内,AT2受体的表达比AT1受体更强。受伤后24小时即可检测到受体表达增强,持续长达3个月。

结论

从这些数据中,我们得出结论,血管紧张素AT1和AT2受体在人类皮肤伤口中上调,进一步支持了血管紧张素II在皮肤伤口愈合早期即发挥作用的概念。

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