دورية أكاديمية

Characterization of transient and progressive pulmonary fibrosis by spatially correlated phase contrast microCT, classical histopathology and atomic force microscopy

التفاصيل البيبلوغرافية
العنوان: Characterization of transient and progressive pulmonary fibrosis by spatially correlated phase contrast microCT, classical histopathology and atomic force microscopy
المؤلفون: D’Amico, Lorenzo, Svetlove, Angelika, Longo, Elena, Meyer, Ruth, Senigagliesi, Beatrice, Saccomano, Giulia, Nolte, Philipp, Wagner, Willi L., Wielpütz, Mark O., Leitz, Dominik H. W., Duerr, Julia, Mall, Marcus A., Casalis, Loredana, Köster, Sarah, Alves, Frauke, Tromba, Giuliana, Dullin, Christian
المساهمون: D’Amico, Lorenzo, Svetlove, Angelika, Longo, Elena, Meyer, Ruth, Senigagliesi, Beatrice, Saccomano, Giulia, Nolte, Philipp, Wagner, Willi L., Wielpütz, Mark O., Leitz, Dominik H. W., Duerr, Julia, Mall, Marcus A., Casalis, Loredana, Köster, Sarah, Alves, Frauke, Tromba, Giuliana, Dullin, Christian
سنة النشر: 2024
المجموعة: Università degli studi di Trieste: ArTS (Archivio della ricerca di Trieste)
مصطلحات موضوعية: AFM, Lung fibrosi, PBI, Spatial correlation, Virtual histology
الوصف: Pulmonary fibrosis (PF) is a severe and progressive condition in which the lung becomes scarred over time resulting in pulmonary function impairment. Classical histopathology remains an important tool for micro-structural tissue assessment in the diagnosis of PF. A novel workflow based on spatial correlated propagation-based phase-contrast micro computed tomography (PBI-microCT), atomic force microscopy (AFM) and histopathology was developed and applied to two different preclinical mouse models of PF - the commonly used and well characterized Bleomycin-induced PF and a novel mouse model for progressive PF caused by conditional Nedd4-2 KO. The aim was to integrate structural and mechanical features from hallmarks of fibrotic lung tissue remodeling. PBI-microCT was used to assess structural alteration in whole fixed and paraffin embedded lungs, allowing for identification of fibrotic foci within the 3D context of the entire organ and facilitating targeted microtome sectioning of planes of interest for subsequent histopathology. Subsequently, these sections of interest were subjected to AFM to assess changes in the local tissue stiffness of previously identified structures of interest. 3D whole organ analysis showed clear morphological differences in 3D tissue porosity between transient and progressive PF and control lungs. By integrating the results obtained from targeted AFM analysis, it was possible to discriminate between the Bleomycin model and the novel conditional Nedd4-2 KO model using agglomerative cluster analysis. As our workflow for 3D spatial correlation of PBI, targeted histopathology and subsequent AFM is tailored around the standard procedure of formalin-fixed paraffin-embedded (FFPE) tissue specimens, it may be a powerful tool for the comprehensive tissue assessment beyond the scope of PF and preclinical research.
نوع الوثيقة: article in journal/newspaper
اللغة: English
العلاقة: info:eu-repo/semantics/altIdentifier/pmid/38211385; volume:169/2024; firstpage:"-"; lastpage:"-"; numberofpages:11; journal:COMPUTERS IN BIOLOGY AND MEDICINE; https://hdl.handle.net/11368/3067762Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85181978515; https://www.sciencedirect.com/science/article/pii/S0010482524000313Test
DOI: 10.1016/j.compbiomed.2024.107947
الإتاحة: https://doi.org/10.1016/j.compbiomed.2024.107947Test
https://hdl.handle.net/11368/3067762Test
https://www.sciencedirect.com/science/article/pii/S0010482524000313Test
حقوق: info:eu-repo/semantics/openAccess
رقم الانضمام: edsbas.D0D44DBC
قاعدة البيانات: BASE