MacKenzie-Graham Allan, Tinsley Matthew R, Shah Kaanan P, Aguilar Cynthia, Strickland Lauren V, Boline Jyl, Martin Melanie, Morales Laurie, Shattuck David W, Jacobs Russell E, Voskuhl Rhonda R, Toga Arthur W
Laboratory of Neuro Imaging, Department of Neurology, University of California-Los Angeles, 635 Charles Young Drive South, Los Angeles, CA 90095-1769, USA.
Neuroimage. 2006 Sep;32(3):1016-23. doi: 10.1016/j.neuroimage.2006.05.006. Epub 2006 Jun 27.
Brain atrophy measured by MRI is an important correlate with clinical disability and disease duration in multiple sclerosis (MS). Unfortunately, neuropathologic mechanisms which lead to this grey matter atrophy remain unknown. The objective of this study was to determine whether brain atrophy occurs in the mouse model, experimental autoimmune encephalomyelitis (EAE). Postmortem high-resolution T2-weighted magnetic resonance microscopy (MRM) images from 32 mouse brains (21 EAE and 11 control) were collected. A minimum deformation atlas was constructed and a deformable atlas approach was used to quantify volumetric changes in neuroanatomical structures. A significant decrease in the mean cerebellar cortex volume in mice with late EAE (48-56 days after disease induction) as compared to normal strain, gender, and age-matched controls was observed. There was a direct correlation between cerebellar cortical atrophy and disease duration. At an early time point in disease, 15 days after disease induction, cerebellar white matter lesions were detected by both histology and MRM. These data demonstrate that myelin-specific autoimmune responses can lead to grey matter atrophy in an otherwise normal CNS. The model described herein can now be used to investigate neuropathologic mechanisms that lead to the development of gray matter atrophy in this setting.
通过磁共振成像(MRI)测量的脑萎缩是多发性硬化症(MS)临床残疾和疾病持续时间的重要相关因素。不幸的是,导致这种灰质萎缩的神经病理机制仍然未知。本研究的目的是确定在实验性自身免疫性脑脊髓炎(EAE)小鼠模型中是否会发生脑萎缩。收集了32只小鼠大脑(21只EAE小鼠和11只对照小鼠)的死后高分辨率T2加权磁共振显微镜(MRM)图像。构建了最小变形图谱,并使用可变形图谱方法来量化神经解剖结构的体积变化。与正常品系、性别和年龄匹配的对照相比,观察到晚期EAE小鼠(疾病诱导后48 - 56天)的平均小脑皮质体积显著减少。小脑皮质萎缩与疾病持续时间之间存在直接相关性。在疾病的早期时间点,即疾病诱导后15天,通过组织学和MRM均检测到小脑白质病变。这些数据表明,髓鞘特异性自身免疫反应可导致原本正常的中枢神经系统发生灰质萎缩。本文所述的模型现在可用于研究导致这种情况下灰质萎缩发展的神经病理机制。