Chilosi Marco, Caliò Anna, Rossi Andrea, Gilioli Eliana, Pedica Federica, Montagna Licia, Pedron Serena, Confalonieri Marco, Doglioni Claudio, Ziesche Rolf, Grubinger Markus, Mikulits Wolfgang, Poletti Venerino
Anatomic Pathology, University and Hospital Trust, Verona, Italy.
Pulmonary Division, University and Hospital Trust, Verona, Italy.
Mod Pathol. 2017 Jan;30(1):26-38. doi: 10.1038/modpathol.2016.147. Epub 2016 Sep 2.
Epithelial to mesenchymal transition has been suggested as a relevant contributor to pulmonary fibrosis, but how and where this complex process is triggered in idiopathic pulmonary fibrosis is not fully understood. Beta-tubulin-III (Tubβ3), ZEB1, and β-catenin are partially under the negative control of miR-200, a family of micro-RNAs playing a major role in epithelial to mesenchymal transition, that are reduced in experimental lung fibrosis and idiopathic pulmonary fibrosis. We wonder whether in situ expression of these proteins is increased in idiopathic pulmonary fibrosis, to better understand the significance of miR-200 feedback loop and epithelial to mesenchymal transition. We investigated the immunohistochemical and immunofluorescent expression and precise location of ZEB1, Tubβ3, and β-catenin in tissue samples from 34 idiopathic pulmonary fibrosis cases and 21 controls (5 normal lungs and 16 other interstitial lung diseases). In 100% idiopathic pulmonary fibrosis samples, the three proteins were concurrently expressed in fibroblastic foci, as well in damaged epithelial cells overlying these lesions and in pericytes within neo-angiogenesis areas. These results were also confirmed by immunofluorescence assay. In controls the abnormal expression of the three proteins was absent or limited. This is the first study that relates concurrent expression of Tubβ3, ZEB1, and β-catenin to abnormal epithelial and myofibroblast differentiation in idiopathic pulmonary fibrosis, providing indirect but robust evidence of miR-200 deregulation and epithelial to mesenchymal transition activation in idiopathic pulmonary fibrosis. The abnormal expression and localization of these proteins in bronchiolar fibro-proliferative lesions are unique for idiopathic pulmonary fibrosis, and might represent a disease-specific marker in challenging lung biopsies.
上皮-间质转化被认为是导致肺纤维化的一个相关因素,但在特发性肺纤维化中,这个复杂过程是如何以及在何处触发的,目前尚未完全清楚。β-微管蛋白III(Tubβ3)、锌指E盒结合蛋白1(ZEB1)和β-连环蛋白部分受微小RNA-200(miR-200)的负调控,miR-200家族在上皮-间质转化中起主要作用,在实验性肺纤维化和特发性肺纤维化中其表达降低。我们想知道这些蛋白在特发性肺纤维化中的原位表达是否增加,以便更好地理解miR-200反馈环以及上皮-间质转化的意义。我们研究了34例特发性肺纤维化病例和21例对照(5例正常肺和16例其他间质性肺疾病)组织样本中ZEB1、Tubβ3和β-连环蛋白的免疫组化和免疫荧光表达及精确位置。在100%的特发性肺纤维化样本中,这三种蛋白同时在成纤维细胞灶中表达,也在这些病变上方受损的上皮细胞以及新生血管区域的周细胞中表达。免疫荧光分析也证实了这些结果。在对照中,这三种蛋白不存在异常表达或仅有有限表达。这是第一项将Tubβ3、ZEB1和β-连环蛋白的同时表达与特发性肺纤维化中异常的上皮和成肌纤维细胞分化联系起来的研究,为特发性肺纤维化中miR-200失调和上皮-间质转化激活提供了间接但有力的证据。这些蛋白在细支气管纤维增生性病变中的异常表达和定位是特发性肺纤维化所特有的,可能是具有挑战性的肺活检中的一种疾病特异性标志物。