Jones Mark G, Fabre Aurélie, Schneider Philipp, Cinetto Francesco, Sgalla Giacomo, Mavrogordato Mark, Jogai Sanjay, Alzetani Aiman, Marshall Ben G, O'Reilly Katherine M A, Warner Jane A, Lackie Peter M, Davies Donna E, Hansell David M, Nicholson Andrew G, Sinclair Ian, Brown Kevin K, Richeldi Luca
Academic Unit of Clinical and Experimental Sciences, Faculty of Medicine, University of Southampton, Southampton, United Kingdom; National Institute for Health Research Respiratory Biomedical Research Unit, University Hospital Southampton, Southampton, United Kingdom.
Department of Histopathology, St. Vincent's University Hospital, Elm Park, Dublin, Ireland.
JCI Insight. 2016 Apr 21;1(5). doi: 10.1172/jci.insight.86375.
In idiopathic pulmonary fibrosis (IPF), the fibroblast focus is a key histological feature representing active fibroproliferation. On standard 2D pathologic examination, fibroblast foci are considered small, distinct lesions, although they have been proposed to form a highly interconnected reticulum as the leading edge of a "wave" of fibrosis. Here, we characterized fibroblast focus morphology and interrelationships in 3D using an integrated micro-CT and histological methodology. In 3D, fibroblast foci were morphologically complex structures, with large variations in shape and volume (range, 1.3 × 10 to 9.9 × 10 μm). Within each tissue sample numerous multiform foci were present, ranging from a minimum of 0.9 per mm of lung tissue to a maximum of 11.1 per mm of lung tissue. Each focus was an independent structure, and no interconnections were observed. Together, our data indicate that in 3D fibroblast foci form a constellation of heterogeneous structures with large variations in shape and volume, suggesting previously unrecognized plasticity. No evidence of interconnectivity was identified, consistent with the concept that foci represent discrete sites of lung injury and repair.
在特发性肺纤维化(IPF)中,成纤维细胞灶是代表活跃纤维增殖的关键组织学特征。在标准的二维病理检查中,成纤维细胞灶被认为是小的、明显的病变,尽管有人提出它们会形成高度相互连接的网状结构,作为纤维化“波”的前沿。在这里,我们使用集成的微型计算机断层扫描(micro-CT)和组织学方法对三维空间中成纤维细胞灶的形态和相互关系进行了表征。在三维空间中,成纤维细胞灶是形态复杂的结构,形状和体积差异很大(范围为1.3×10至9.9×10μm)。在每个组织样本中都存在大量形态多样的病灶,每毫米肺组织中最少有0.9个,最多有11.1个。每个病灶都是一个独立的结构,未观察到相互连接。总之,我们的数据表明,在三维空间中,成纤维细胞灶形成了一组形状和体积差异很大的异质结构,这表明存在以前未被认识到的可塑性。未发现相互连接的证据,这与病灶代表肺损伤和修复的离散部位这一概念一致。