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人体离体创面模型及全器官染色方法准确评估皮肤修复效果。

Human Ex vivo Wound Model and Whole-Mount Staining Approach to Accurately Evaluate Skin Repair.

机构信息

Centre for Atherothrombosis and Metabolic Disease, Hull York Medical School, University of Hull;

Centre for Atherothrombosis and Metabolic Disease, Hull York Medical School, University of Hull.

出版信息

J Vis Exp. 2021 Feb 17(168). doi: 10.3791/62326.

Abstract

Chronic non-healing wounds, which primarily affect the elderly and diabetic, are a significant area of clinical unmet need. Unfortunately, current chronic wound treatments are inadequate, while available pre-clinical models poorly predict the clinical efficacy of new therapies. Here we describe a high throughput, pre-clinical model to assess multiple aspects of the human skin repair response. Partial thickness wounds were created in human ex vivo skin and cultured across a healing time course. Skin wound biopsies were collected in fixative for the whole-mount staining procedure. Fixed samples were blocked and incubated in primary antibody, with detection achieved via fluorescently conjugated secondary antibody. Wounds were counterstained and imaged via confocal microscopy before calculating percentage wound closure (re-epithelialization) in each biopsy. Applying this protocol, we reveal that 2 mm excisional wounds created in healthy donor skin are fully re-epithelialized by day 4-5 post-wounding. On the contrary, closure rates of diabetic skin wounds are significantly reduced, accompanied by perturbed barrier reformation. Combining human skin wounding with a novel whole-mount staining approach allows a rapid and reproducible method to quantify ex vivo wound repair. Collectively, this protocol provides a valuable human platform to evaluate the effectiveness of potential wound therapies, transforming pre-clinical testing and validation.

摘要

慢性难愈性伤口主要影响老年人和糖尿病患者,是临床未满足需求的一个重要领域。不幸的是,目前的慢性伤口治疗方法并不充分,而现有的临床前模型也不能很好地预测新疗法的临床疗效。在这里,我们描述了一种高通量的临床前模型,用于评估人类皮肤修复反应的多个方面。在人体离体皮肤中制造部分厚度的伤口,并在整个愈合过程中进行培养。在固定剂中收集皮肤伤口活检样本,用于全层染色程序。固定后的样本经过封闭和一抗孵育,通过荧光标记的二抗进行检测。对伤口进行复染并通过共聚焦显微镜成像,然后计算每个活检中的伤口闭合百分比(再上皮化)。应用该方案,我们发现健康供体皮肤中 2 毫米的切除性伤口在创伤后 4-5 天即可完全再上皮化。相反,糖尿病皮肤伤口的闭合率显著降低,同时伴有屏障重建紊乱。将人体皮肤创伤与新型全层染色方法相结合,提供了一种快速且可重复的方法来定量评估离体伤口修复。总的来说,该方案为评估潜在伤口治疗方法的有效性提供了一个有价值的人体平台,改变了临床前测试和验证。

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