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首页> 外文期刊>International Journal of Radiation Biology: Covering the Physical, Chemical, Biological, and Medical Effects of Ionizing and Non-ionizing Radiations >Immunohistochemical evidence for the occurrence of similar epithelial phenotypes during lung development and radiation-induced fibrogenesis.
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Immunohistochemical evidence for the occurrence of similar epithelial phenotypes during lung development and radiation-induced fibrogenesis.

机译:免疫组织化学证据表明,在肺发育和辐射诱导的纤维形成过程中,出现了相似的上皮表型。

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PURPOSE: Processes of fibrosis, wound healing and tissue regeneration have in common the fact that proliferation and differentiation of cells involved in the restoration of normal-tissue architecture resemble to a certain degree the embryonic development of the corresponding tissue. The present review focuses on the phenotypic changes of alveolar epithelial cells during fibrogenesis and describes similarities in the expression pattern of epithelial antigens during lung development. METHODS: For comparative studies, immunohistochemical investigations of different experimental fibrosis models were performed. RESULTS: For several epithelial proteins, such as the CD44 adhesion molecule, the enzymes carbanhydrase II and cathepsin D, as well as the lectin galectin-3, a transient epithelial immunoreactivity have been detected. What all four examples have in common is that a part of the foetal antigenic profile reappears under conditions of injury and during the development of pulmonary fibrosis. CONCLUSIONS: The re-expression of foetal antigens in fibrotic samples with a spatio-temporal pattern, as detected by immunocytochemical techniques, indicates that some mechanisms or factors exist, which similarly regulate the differentiation of the epithelium during ontogenesis and in the remodelling process during fibrogenesis.
机译:目的:纤维化,伤口愈合和组织再生的过程共有一个事实,即参与正常组织结构恢复的细胞的增殖和分化在一定程度上类似于相应组织的胚胎发育。本文综述了纤维化过程中肺泡上皮细胞的表型变化,并描述了肺发育过程中上皮抗原表达模式的相似性。方法:为了进行比较研究,对不同的实验性纤维化模型进行了免疫组织化学研究。结果:对于几种上皮蛋白,例如CD44粘附分子,碳氢酶II和组织蛋白酶D以及凝集素半乳凝素3,已经检测到短暂的上皮免疫反应性。这四个例子的共同点是,胎儿的抗原谱的一部分会在受伤的情况下以及在肺纤维化的发展过程中重新出现。结论:通过免疫细胞化学技术检测到的具有时空分布的纤维化样品中胎儿抗原的重新表达,表明存在一些机制或因素,这些机制或调控因素类似地调控了本体形成过程中以及纤维形成过程中重塑过程中上皮的分化。 。

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