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研究人类肥厚性瘢痕及其他皮肤纤维化的新方法。

Novel methods for the investigation of human hypertrophic scarring and other dermal fibrosis.

作者信息

Honardoust Dariush, Kwan Peter, Momtazi Moein, Ding Jie, Tredget Edward E

机构信息

Wound Healing Research Group, Plastic Surgery Research Laboratory, Department of Surgery, University of Alberta, Edmonton, AB, Canada.

出版信息

Methods Mol Biol. 2013;1037:203-31. doi: 10.1007/978-1-62703-505-7_11.

Abstract

Hypertrophic scar (HTS) represents the dermal equivalent of fibroproliferative disorders that occur after injury involving the deep dermis while superficial wounds to the skin heal with minimal or no scarring. HTS is characterized by progressive deposition of collagen that occurs with high frequency in adult dermal wounds following traumatic or thermal injury. Increased levels of transforming growth factor-β1 (TGF-β1), decreased expression of small leucine-rich proteoglycans (SLRPs), and/or fibroblast subtypes may influence the development of HTS. The development of HTS is strongly influenced by the cellular and molecular properties of fibroblast subtypes, where cytokines such as fibrotic TGF-β1 and CTGF as well as the expression of SLRPs, particularly decorin and fibromodulin, regulate collagen fibrillogenesis and the activity of TGF-β1. Reduced anti-fibrotic molecules in the ECM of the deep dermis and the distinctive behavior of the fibroblasts in this region of the dermis which display increased sensitivity to TGF-β1's biological activity contribute to the development of HTS following injury to the deep dermis. By comparing the cellular and molecular differences involved in deep and superficial wound healing in an experimental wound scratch model in humans that has both superficial and deep injuries within the same excisional model, our aim is to increase our understanding of how tissue repair following injury to the deep dermis can be changed to promote healing with a similar pattern to healing that occurs following superficial injury that results in no or minimal scarring. Studying the characteristics of superficial dermal injuries that heal with minimal scarring will help us identify therapeutic approaches for tissue engineering and wound healing. In addition, our ability to develop novel therapies for HTS is hampered by limitations in the available animal models used to study this disorder in vivo. We also describe a nude mouse model of transplanted human skin that develops a hypertrophic proliferative scar consistent morphologically and histologically with human HTS, which can be used to test novel treatment options for these dermal fibrotic conditions.

摘要

肥厚性瘢痕(HTS)是一种真皮层的纤维增生性疾病,发生于涉及深层真皮的损伤之后,而皮肤的浅表伤口愈合时瘢痕形成极少或无瘢痕形成。HTS的特征是胶原蛋白进行性沉积,在成人真皮创伤或热损伤后的伤口中高频发生。转化生长因子-β1(TGF-β1)水平升高、富含亮氨酸的小分子蛋白聚糖(SLRPs)表达降低和/或成纤维细胞亚型可能影响HTS的发展。HTS的发展受到成纤维细胞亚型的细胞和分子特性的强烈影响,其中诸如促纤维化的TGF-β1和结缔组织生长因子(CTGF)等细胞因子以及SLRPs的表达,特别是核心蛋白聚糖和纤调蛋白,调节胶原纤维形成和TGF-β1的活性。深层真皮细胞外基质中抗纤维化分子的减少以及该真皮区域中成纤维细胞的独特行为,即对TGF-β1的生物活性表现出更高的敏感性,导致深层真皮损伤后HTS的发展。通过在人类实验性伤口划痕模型中比较深层和浅表伤口愈合所涉及的细胞和分子差异,该模型在同一切除模型中既有浅表损伤又有深层损伤,我们的目的是增进对深层真皮损伤后组织修复如何改变以促进愈合的理解,使其愈合模式类似于浅表损伤后无瘢痕或极少瘢痕形成的愈合模式。研究以极少瘢痕愈合的浅表真皮损伤的特征将有助于我们确定组织工程和伤口愈合的治疗方法。此外,用于体内研究这种疾病的现有动物模型的局限性阻碍了我们开发针对HTS的新疗法的能力。我们还描述了一种移植人类皮肤的裸鼠模型,该模型形成形态和组织学上与人类HTS一致的肥厚性增殖性瘢痕,可用于测试针对这些真皮纤维化病症的新治疗方案。

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