Meyer Cassandra E, Gao Josephine L, Cheng James Ying-Jie, Oberoi Mandavi R, Johnsonbaugh Hadley, Lepore Stefano, Kurth Florian, Thurston Mackenzie J, Itoh Noriko, Patel Kevin R, Voskuhl Rhonda R, MacKenzie-Graham Allan
Ahmanson-Lovelace Brain Mapping Center, Department of Neurology, David Geffen School of Medicine, UCLA, Los Angeles, CA, USA/ UCLA Multiple Sclerosis Program, Department of Neurology, David Geffen School of Medicine, UCLA, Los Angeles, CA, USA.
UCLA Multiple Sclerosis Program, Department of Neurology, David Geffen School of Medicine, UCLA, Los Angeles, CA, USA.
Mult Scler. 2020 Mar;26(3):294-303. doi: 10.1177/1352458519830614. Epub 2019 Mar 7.
Gray matter (GM) atrophy in brain is one of the best predictors of long-term disability in multiple sclerosis (MS), and recent findings have revealed that localized GM atrophy is associated with clinical disabilities. GM atrophy associated with each disability mapped to a distinct brain region, revealing a disability-specific atlas (DSA) of GM loss.
To uncover the mechanisms underlying the development of localized GM atrophy.
We used voxel-based morphometry (VBM) to evaluate localized GM atrophy and Clear Lipid-exchanged Acrylamide-hybridized Rigid Imaging-compatible Tissue-hYdrogel (CLARITY) to evaluate specific pathologies in mice with experimental autoimmune encephalomyelitis (EAE).
We observed extensive GM atrophy throughout the cerebral cortex, with additional foci in the thalamus and caudoputamen, in mice with EAE compared to normal controls. Next, we generated pathology-specific atlases (PSAs), voxelwise mappings of the correlation between specific pathologies and localized GM atrophy. Interestingly, axonal damage (end-bulbs and ovoids) in the spinal cord strongly correlated with GM atrophy in the sensorimotor cortex of the brain.
The combination of VBM with CLARITY in EAE can localize GM atrophy in brain that is associated with a specific pathology in spinal cord, revealing a PSA of GM loss.
脑灰质(GM)萎缩是多发性硬化症(MS)长期残疾的最佳预测指标之一,最近的研究结果表明,局部GM萎缩与临床残疾相关。与每种残疾相关的GM萎缩映射到不同的脑区,揭示了GM丢失的残疾特异性图谱(DSA)。
揭示局部GM萎缩发展的潜在机制。
我们使用基于体素的形态计量学(VBM)来评估局部GM萎缩,并使用透明脂质交换丙烯酰胺杂交刚性成像兼容组织水凝胶(CLARITY)来评估实验性自身免疫性脑脊髓炎(EAE)小鼠的特定病理。
与正常对照组相比,我们观察到EAE小鼠的整个大脑皮质广泛存在GM萎缩,丘脑和尾状壳核有额外的病灶。接下来,我们生成了病理特异性图谱(PSA),即特定病理与局部GM萎缩之间相关性的体素映射。有趣的是,脊髓中的轴突损伤(终球和卵圆形)与大脑感觉运动皮质中的GM萎缩密切相关。
在EAE中,VBM与CLARITY相结合可以定位与脊髓特定病理相关的脑内GM萎缩,揭示GM丢失的PSA。