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从整体器官成像到计算机血流建模:一种新的多尺度网络分析方法,用于重新研究组织功能解剖。

From whole-organ imaging to in-silico blood flow modeling: A new multi-scale network analysis for revisiting tissue functional anatomy.

机构信息

Institute of Fluid Mechanics of Toulouse (IMFT), Toulouse University, CNRS, INPT, UPS, Toulouse, France.

CNRS 5273; UMR STROMALab, BP 84225, F-31 432 Toulouse Cedex 4, France.

出版信息

PLoS Comput Biol. 2020 Feb 14;16(2):e1007322. doi: 10.1371/journal.pcbi.1007322. eCollection 2020 Feb.

Abstract

We present a multi-disciplinary image-based blood flow perfusion modeling of a whole organ vascular network for analyzing both its structural and functional properties. We show how the use of Light-Sheet Fluorescence Microscopy (LSFM) permits whole-organ micro-vascular imaging, analysis and modelling. By using adapted image post-treatment workflow, we could segment, vectorize and reconstruct the entire micro-vascular network composed of 1.7 million vessels, from the tissue-scale, inside a ∼ 25 × 5 × 1 = 125mm3 volume of the mouse fat pad, hundreds of times larger than previous studies, down to the cellular scale at micron resolution, with the entire blood perfusion modeled. Adapted network analysis revealed the structural and functional organization of meso-scale tissue as strongly connected communities of vessels. These communities share a distinct heterogeneous core region and a more homogeneous peripheral region, consistently with known biological functions of fat tissue. Graph clustering analysis also revealed two distinct robust meso-scale typical sizes (from 10 to several hundred times the cellular size), revealing, for the first time, strongly connected functional vascular communities. These community networks support heterogeneous micro-environments. This work provides the proof of concept that in-silico all-tissue perfusion modeling can reveal new structural and functional exchanges between micro-regions in tissues, found from community clusters in the vascular graph.

摘要

我们提出了一种多学科的基于图像的全器官血管网络血流灌注建模方法,用于分析其结构和功能特性。我们展示了如何使用光片荧光显微镜(LSFM)来实现全器官微血管成像、分析和建模。通过使用适应性的图像后处理工作流程,我们可以分割、矢量化和重建整个微血管网络,该网络由 170 万个血管组成,来自于组织尺度,在小鼠脂肪垫内约 25×5×1=125mm3 的体积内,比以前的研究大数百倍,达到微米分辨率的细胞尺度,整个血液灌注都被建模。适应性的网络分析揭示了中尺度组织的结构和功能组织,作为血管强烈连接的社区。这些社区共享一个独特的异质核心区域和一个更均匀的外围区域,与脂肪组织的已知生物学功能一致。图聚类分析还揭示了两个不同的稳健中尺度典型大小(从细胞大小的 10 倍到几百倍),首次揭示了功能血管社区的强烈连接。这些社区网络支持异质的微环境。这项工作提供了概念验证,即体内全组织灌注建模可以揭示组织中微区域之间新的结构和功能交换,这些交换是从血管图中的社区聚类中发现的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/53b3/7062279/2e754f2083df/pcbi.1007322.g001.jpg

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