Hassmann-Poznańska Elżbieta, Taranta Andrzej, Bialuk Izabela, Poznańska Maria, Zajączkiewicz Hanna, Winnicka Maria Małgorzata
Department of Pediatric Otolaryngology, Medical University of Białystok, Waszyngtona 17, 15-274 Białystok, Poland.
Int J Pediatr Otorhinolaryngol. 2013 Oct;77(10):1753-9. doi: 10.1016/j.ijporl.2013.08.009. Epub 2013 Aug 21.
The goal of this work was to identify genes, known to be involved in the skin wound healing, that express differentially in the healthy and injured tympanic membrane (TM), and designate the molecules potentially beneficial for treatment of TM perforation. The molecular mechanisms controlling the course of TM regeneration are far from being elucidated.
Twenty rats had their tympanic membranes perforated, while four served as a control. Animals were sacrificed on either days 1, 2, 3, 5 and 10 post injury, and TMs were immediately dissected and frozen in liquid nitrogen. Total TM RNA was isolated and reversely transcribed. qPCR was performed using Rat Wound Healing RT(2) Profiler PCR Array (QIAGEN) containing primers for 84 genes.
Statistically significant changes in the expression of 42 genes were found in various stages of TM healing. The increased expression of genes taking part in the inflammatory reaction (interleukin 6, granulocyte and macrophage chemotactic proteins) was observed from day 2. The expression of several genes of extracellular matrix components and their remodeling enzymes was also changed. Among growth factor genes: Vegfa, Igf1 and Hbegf showed increased expression at the beginning of the healing process, while Hgf expression was highest on day 3.
Several changes in the expression of genes involved in remodeling of extracellular matrix point to important role of connective tissue in TM healing. The molecules accelerating this process, like HbEGF and HGF, seem to be good candidates for further evaluation of their possible use in clinical treatment.
本研究旨在鉴定已知参与皮肤伤口愈合且在健康和受损鼓膜(TM)中差异表达的基因,并确定可能对鼓膜穿孔治疗有益的分子。控制鼓膜再生过程的分子机制尚未完全阐明。
20只大鼠鼓膜穿孔,4只作为对照。在受伤后第1、2、3、5和10天处死动物,立即解剖鼓膜并在液氮中冷冻。分离总鼓膜RNA并进行逆转录。使用包含84个基因引物的大鼠伤口愈合RT(2) Profiler PCR阵列(QIAGEN)进行qPCR。
在鼓膜愈合的各个阶段发现42个基因的表达有统计学显著变化。从第2天开始观察到参与炎症反应的基因(白细胞介素6、粒细胞和巨噬细胞趋化蛋白)表达增加。细胞外基质成分及其重塑酶的几个基因的表达也发生了变化。在生长因子基因中:Vegfa、Igf1和Hbegf在愈合过程开始时表达增加,而Hgf在第3天表达最高。
细胞外基质重塑相关基因表达的若干变化表明结缔组织在鼓膜愈合中起重要作用。加速这一过程的分子,如HbEGF和HGF,似乎是进一步评估其在临床治疗中可能用途的良好候选者。