用光栅扫描光声介观镜对小鼠肾脏血管系统进行高分辨率无标签测绘:一项离体研究。

IF 2.4 Q1 PEDIATRICS
Colin A Goebel, Emma Brown, Fabian B Fahlbusch, Alexandra L Wagner, Adrian Buehler, Thomas Raupach, Martin Hohmann, Moritz Späth, Neal Burton, Joachim Woelfle, Michael Schmidt, Andrea Hartner, Adrian P Regensburger, Ferdinand Knieling
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引用次数: 1

摘要

背景:慢性肾脏疾病(CKD)是影响儿童和成人的全球性负担。新的成像方式对可视化和量化结构、功能和分子器官损伤有很大的希望。本研究的目的是利用无标记光栅扫描光声mesoscopy (RSOM)对小鼠肾损伤移植器官进行可视化和定量观察。材料和方法:实验采用α 8整合素敲除小鼠(KO)和野生型小鼠(WT)新鲜切肾。采用RSOM光声成像系统(RSOM Explorer P50在SWL 532nm和/或ms-P50成像系统在532nm、555 nm、579 nm和606 nm)对6周龄雌性动物n=7 (n=4 KO, n=3 WT)和雄性动物n=6 (n=2 KO, n=4 WT)进行检测。使用专用软件重建图像,分析大小和血管面积,并与标准组织学切片进行比较。结果:RSOM实现了小鼠肾脏大小和血管面积的制图,揭示了雄性小鼠(m)和雌性小鼠(f)肾脏大小(合并频率(MF) f比m: 52.42±6.24 mm2比69.18±15.96 mm2, p=0.0156)和绝对血管面积(MF f比m: 35.67±4.22 mm2比49.07±13.48 mm2, p=0.0036)的差异。与性别无关,敲除型(KO)小鼠的绝对肾脏面积比野生型(WT)小鼠小(WT vs. KO: MF: p=0.0255),相对血管面积也呈现类似趋势(WT vs. KO: MF p=0.0031)。与WT相比,KO的绝对血管面积也有显著差异(MF p=0.0089)。与WT雄性小鼠相比,KO的绝对血管面积显著减少(MF WT vs. KO: 54.37±9.35 mm2 vs. 34.93±13.82 mm2, p=0.0232)。此外,通过光谱分解,多光谱RSOM可以可视化氧化和脱氧实质区域。结论:本研究证明了RSOM能够在高分辨率下无标记地显示小鼠离体肾组织血管形态的差异。由于其可扩展性,光声成像提供了一种具有进一步临床前和临床成像应用潜力的新兴模式。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

High-resolution label-free mapping of murine kidney vasculature by raster-scanning optoacoustic mesoscopy: an ex vivo study.

High-resolution label-free mapping of murine kidney vasculature by raster-scanning optoacoustic mesoscopy: an ex vivo study.

High-resolution label-free mapping of murine kidney vasculature by raster-scanning optoacoustic mesoscopy: an ex vivo study.

High-resolution label-free mapping of murine kidney vasculature by raster-scanning optoacoustic mesoscopy: an ex vivo study.

Background: Chronic kidney disease (CKD) is a global burden affecting both children and adults. Novel imaging modalities hold great promise to visualize and quantify structural, functional, and molecular organ damage. The aim of the study was to visualize and quantify murine renal vasculature using label-free raster scanning optoacoustic mesoscopy (RSOM) in explanted organs from mice with renal injury.

Material and methods: For the experiments, freshly bisected kidneys of alpha 8 integrin knock-out (KO) and wildtype mice (WT) were used. A total of n=7 female (n=4 KO, n=3 WT) and n=6 male animals (n=2 KO, n=4 WT) aged 6 weeks were examined with RSOM optoacoustic imaging systems (RSOM Explorer P50 at SWL 532nm and/or ms-P50 imaging system at 532 nm, 555 nm, 579 nm, and 606 nm). Images were reconstructed using a dedicated software, analyzed for size and vascular area and compared to standard histologic sections.

Results: RSOM enabled mapping of murine kidney size and vascular area, revealing differences between kidney sizes of male (m) and female (f) mice (merged frequencies (MF) f vs. m: 52.42±6.24 mm2 vs. 69.18±15.96 mm2, p=0.0156) and absolute vascular area (MF f vs. m: 35.67±4.22 mm2 vs. 49.07±13.48 mm2, p=0.0036). Without respect to sex, the absolute kidney area was found to be smaller in knock-out (KO) than in wildtype (WT) mice (WT vs. KO: MF: p=0.0255) and showed a similar trend for the relative vessel area (WT vs. KO: MF p=0.0031). Also the absolute vessel areas of KO compared to WT were found significantly different (MF p=0.0089). A significant decrease in absolute vessel area was found in KO compared to WT male mice (MF WT vs. KO: 54.37±9.35 mm2 vs. 34.93±13.82 mm2, p=0.0232). In addition, multispectral RSOM allowed visualization of oxygenated and deoxygenated parenchymal regions by spectral unmixing.

Conclusion: This study demonstrates the capability of RSOM for label-free visualization of differences in vascular morphology in ex vivo murine renal tissue at high resolution. Due to its scalability optoacoustic imaging provides an emerging modality with potential for further preclinical and clinical imaging applications.

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