Norwegian University of Science and Technology, Department of Physics, Faculty of Natural Sciences and Technology, Trondheim, Norway.
J Biomed Opt. 2013 Oct;18(10):101313. doi: 10.1117/1.JBO.18.10.101313.
A spectral correlation algorithm for the analysis of hyperspectral fluorescence images is proposed by Ellingsen et al. [J. Biomed. Opt. 18, 020501 (2013)]. Here, it is applied to the analysis of double-stained Aβ amyloid plaques being related to the Alzheimer's disease (AD). Sections of APP/PS1 AD mice model brains are double stained with luminescent-conjugated oligothiophenes, known to bind to amyloid protein deposits. Hyperspectral fluorescence images of the brain sections are recorded and by applying the correlation algorithm the spectral inhomogeneity of the double-stained samples is mapped in terms of radial distribution and spectral content. To further investigate the progression of Aβ amyloid plaque formation, 19 AD mice of different ages up to 23 months are characterized, enabling a statistical analysis of the plaque heterogeneity. In accordance with recent findings by Nyström et al. [ACS Chem. Biol. 8, 1128-1133 (2013)], the spectral distribution within Aβ plaques is found to vary with age throughout the lifespan of the mouse. With the new correlation algorithm, it is possible to quantify the spectral abundance of the two stains depending on the relative distance from the plaque center and mouse age. Thus, we demonstrate the use of the correlation analysis approach in double-staining experiments and how it is possible to relate these to structural/spectral changes in biological samples.
埃林森等人提出了一种用于分析高光谱荧光图像的光谱相关算法。[J. 生物医学光学。18, 020501 (2013)]。在这里,它被应用于与阿尔茨海默病(AD)相关的双染 Aβ 淀粉样斑块的分析。用发光偶联的寡聚噻吩对 APP/PS1 AD 小鼠模型脑切片进行双染,已知这些寡聚噻吩与淀粉样蛋白沉积物结合。记录脑切片的高光谱荧光图像,并通过应用相关算法,以径向分布和光谱内容的形式绘制双染样品的光谱不均匀性。为了进一步研究 Aβ 淀粉样斑块形成的进展,对 19 只不同年龄的 AD 小鼠进行了特征分析,直至 23 个月大,从而可以对斑块异质性进行统计分析。与 Nyström 等人的最近发现一致。[ACS 化学生物学。8, 1128-1133 (2013)],在小鼠的整个生命周期内,Aβ 斑块内的光谱分布随年龄而变化。通过新的相关算法,可以根据与斑块中心的相对距离和小鼠年龄来量化两种染色剂的光谱丰度。因此,我们展示了相关分析方法在双染实验中的应用,以及如何将其与生物样本的结构/光谱变化联系起来。