Expression of MMP1 in surgical and radiation-impaired wound healing and its effects on the healing process.

Q. Gu, De-wen Wang, Ya-bin Gao, Jie Zhou, R. Peng, Yufang Cui, G. Xia, Quanhong Qing, Hong Yang, Jie Liu, Mei-lan Zhao
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引用次数: 46

Abstract

Radiation-impaired wound is characterized by delayed healing, nonhealing, and carcinogenesis. The mechanism remains unclear. Matrix metalloproteinases (MMPs) are one family of key regulators of the process of wound healing. Their abnormal expression plays important roles in the formation of some chronic skin ulcers. The objective of this project was to study the expression of MMP1 in surgical and radiation-impaired wound healing and its effects on the healing process and tissue remodeling. A rat model of radiation-impaired wound healing was used. Routine light microscopy, electron microscopy, immunohistochemistry, and in situ hybridization, all of which enabled the detection of MMP1 expression during the healing process, were performed. The wound healing process was impaired and delayed. In rats receiving 25Gy gamma-ray locally, the irradiated wounds healed 6 days later than the nonirradiated controls. The following changes in MMP1 expression were found: (1) In the early inflammatory phase and in the period of granulation tissue formation, MMP1 expression was only slightly if at all affected in the newly formed epidermis of irradiated wounds compared with controls. Later, the epidermal expression of MMP1 in radiation wounds was comparatively increased following the delay of the healing process. (2) MMP1 expression in irradiated wounds was markedly decreased in fibroblasts, endothelial cells, and macrophages compared with controls. The expression phase was prolonged because of the delay of the healing process. The reduced expression of MMP1 in granulation tissue retards such important processes as cell migration, angiogenesis, and tissue remodeling, thus slowing the healing process. The expression ofMMP1 in the proliferating keratinocytes may help re-epithelialization. However, in the late healing period, overexpression of MMP1 in the epidermis may hinder the establishment of basal membrane and the formation of granulation tissue, and affect the tissue remodeling process.
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MMP1在外科和放射损伤伤口愈合中的表达及其对愈合过程的影响。
辐射损伤伤口的特点是愈合延迟、不愈合和致癌。其机制尚不清楚。基质金属蛋白酶(Matrix metalloproteinases, MMPs)是伤口愈合过程的关键调控因子之一。它们的异常表达在一些慢性皮肤溃疡的形成中起重要作用。本项目旨在研究MMP1在外科和放射损伤创面愈合中的表达及其对愈合过程和组织重塑的影响。采用大鼠放射损伤创面愈合模型。进行常规光镜、电镜、免疫组织化学和原位杂交,所有这些都能检测到愈合过程中MMP1的表达。伤口愈合过程受损和延迟。局部接受25Gy γ射线照射的大鼠伤口愈合时间比未照射对照组晚6天。MMP1的表达变化如下:(1)与对照组相比,在炎症早期和肉芽组织形成时期,辐照创面新形成表皮中MMP1的表达即使有影响,也只有轻微的变化。随后,随着愈合过程的延迟,MMP1在辐射创面表皮的表达相对增加。(2)与对照组相比,MMP1在辐照创面成纤维细胞、内皮细胞和巨噬细胞中的表达明显降低。由于愈合过程的延迟,表达期延长。肉芽组织中MMP1表达的减少会阻碍细胞迁移、血管生成和组织重塑等重要过程,从而减缓愈合过程。mmp1在增殖的角质形成细胞中的表达可能有助于再上皮化。然而,在愈合后期,表皮中MMP1的过度表达可能会阻碍基膜的建立和肉芽组织的形成,并影响组织重塑过程。
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