纤溶酶原激活物和抑制物在大鼠鼓膜穿孔愈合中的表达增强。

IF 2.4 3区 医学 Q3 NEUROSCIENCES
Maria Makuszewska, Magdalena Cieślińska, Maria M Winnicka, Bożena Skotnicka, Kazimierz Niemczyk, Tomasz Bonda
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引用次数: 0

摘要

在鼓膜(TM)愈合过程中纤溶酶原激活的重要性主要是通过对敲除小鼠进行的研究而知道的。在之前的研究中,我们报道了纤溶酶原激活和抑制系统基因编码蛋白在大鼠TM穿孔愈合中的激活。本研究的目的是在损伤后10天的观察期,分别用免疫印迹法和免疫荧光法评价这些基因表达的蛋白产物及其组织分布。采用耳镜和组织学评价评价愈合过程。尿激酶纤溶酶原激活物(uPA)及其受体(uPAR)的表达在增殖期显著上调,随后在愈合过程的重塑期逐渐衰减,此时角质形成细胞迁移减弱。纤溶酶原激活物抑制剂1型(PAI-1)的表达也在增殖期达到最高水平。组织型纤溶酶原激活物(tPA)表达在整个观察期内均呈升高趋势,以重塑期活性最高。这些蛋白的免疫荧光主要存在于迁移上皮中。我们的研究发现,纤溶酶原激活(uPA, uPAR, tPA)和抑制(PAI-1)分子形成了一个结构良好的上皮迁移调控系统,这对TM穿孔后的愈合至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Enhanced Expression of Plasminogen Activators and Inhibitor in the Healing of Tympanic Membrane Perforation in Rats.

Enhanced Expression of Plasminogen Activators and Inhibitor in the Healing of Tympanic Membrane Perforation in Rats.

Enhanced Expression of Plasminogen Activators and Inhibitor in the Healing of Tympanic Membrane Perforation in Rats.

Enhanced Expression of Plasminogen Activators and Inhibitor in the Healing of Tympanic Membrane Perforation in Rats.

The significance of plasminogen activation during the tympanic membrane (TM) healing is known mainly from studies performed on knock-out mice. In the previous study, we reported activation of genes coding proteins of plasminogen activation and inhibition system in rat's TM perforation healing. The aim of the present study was the evaluation of protein products expressed by these genes and their tissue distribution using Western blotting and immunofluorescent method, respectively, during 10-day observation period after injury. Otomicroscopical and histological evaluation were employed to assess the healing process. The expression of urokinase plasminogen activator (uPA) and its receptor (uPAR) were significantly upregulated in the proliferation phase, with subsequent gradual attenuation during remodeling phase of healing process, when keratinocyte migration was weakening. The expression of plasminogen activator inhibitor type 1 (PAI-1) also showed the highest levels during the proliferation phase. The increase of tissue plasminogen activator (tPA) expression was observed during the whole observation period, with the highest activity during the remodeling phase. Immunofluorescence of these proteins was present mainly in migrating epithelium. Our study found that plasminogen activation (uPA, uPAR, tPA) and inhibitory (PAI-1) molecules form a well-structured regulatory system of the epithelial migration that is critical to the healing of TM after its perforation.

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来源期刊
CiteScore
4.10
自引率
12.50%
发文量
57
审稿时长
6-12 weeks
期刊介绍: JARO is a peer-reviewed journal that publishes research findings from disciplines related to otolaryngology and communications sciences, including hearing, balance, speech and voice. JARO welcomes submissions describing experimental research that investigates the mechanisms underlying problems of basic and/or clinical significance. Authors are encouraged to familiarize themselves with the kinds of papers carried by JARO by looking at past issues. Clinical case studies and pharmaceutical screens are not likely to be considered unless they reveal underlying mechanisms. Methods papers are not encouraged unless they include significant new findings as well. Reviews will be published at the discretion of the editorial board; consult the editor-in-chief before submitting.
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