实验性自身免疫性脑脊髓炎
视网膜
CX3CR1型
视网膜
医学
小胶质细胞
共焦
病理
多发性硬化
脑脊髓炎
髓鞘少突胶质细胞糖蛋白
免疫学
眼科
趋化因子
神经科学
炎症
趋化因子受体
生物
几何学
数学
作者
Moritz J. Frenger,Christina Hecker,Mustafa Sindi,Andrea Issberner,Hans‐Peter Hartung,Sven G. Meuth,Michael Dietrich,Philipp Albrecht
标识
DOI:10.3389/fimmu.2021.761776
摘要
Confocal scanning laser ophthalmoscopy (cSLO) is a non-invasive technique for real-time imaging of the retina. We developed a step-by-step protocol for the semi-automatic evaluation of myeloid cells in cSLO images from CX3CR1 GFP mice, expressing green fluorescent protein (GFP) under control of the endogenous CX3C chemokine receptor 1 locus. We identified cSLO parameters allowing us to distinguish animals with experimental autoimmune encephalomyelitis (EAE) from sham-treated/naïve animals. Especially cell count (CC) and the total microglial area (SuA) turned out to be reliable parameters. Comparing the cSLO results with clinical parameters, we found significant correlations between the clinical EAE score and the SuA and of the inner retinal layer thickness, measured by optical coherence tomography, with the CC as well as the SuA. As a final step, we performed immunohistochemistry to confirm that the GFP-expressing cells visualized by the cSLO are Iba1 positive and validated the step-by-step protocol against manual counting. We present a semi-automatic step-by-step protocol with a balance between fast data evaluation and adequate accuracy, which is optimized by the option to manually adapt the contrast threshold. This protocol may be useful for numerous research questions on the role of microglial polarization in models of inflammatory and degenerating CNS diseases involving the retina.
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