Jack Clifford R, Garwood Michael, Wengenack Thomas M, Borowski Bret, Curran Geoffrey L, Lin Joseph, Adriany Gregor, Gröhn Olli H J, Grimm Roger, Poduslo Joseph F
Department of Radiology, Mayo Clinic College of Medicine, Rochester, Minnesota 55905, USA.
Magn Reson Med. 2004 Dec;52(6):1263-71. doi: 10.1002/mrm.20266.
One of the cardinal pathologic features of Alzheimer's disease (AD) is the formation of senile, or amyloid, plaques. Transgenic mice have been developed that express one or more of the genes responsible for familial AD in humans. Doubly transgenic mice develop "human-like" plaques, providing a mechanism to study amyloid plaque biology in a controlled manner. Imaging of labeled plaques has been accomplished with other modalities, but only MRI has sufficient spatial and contrast resolution to visualize individual plaques noninvasively. Methods to optimize visualization of plaques in vivo in transgenic mice at 9.4 T using a spin echo sequence based on adiabatic pulses are described. Preliminary results indicate that a spin echo acquisition more accurately reflects plaque size, while a T2* weighted gradient echo sequence reflects plaque iron content, not plaque size. In vivo MRI-ex vivo MRI-in vitro histologic correlations are provided. Histologically verified plaques as small as 50 microm in diameter were visualized in living animals. To our knowledge this work represents the first demonstration of noninvasive in vivo visualization of individual AD plaques without the use of a contrast agent.
阿尔茨海默病(AD)的主要病理特征之一是老年斑或淀粉样斑块的形成。已经培育出了表达人类家族性AD相关一种或多种基因的转基因小鼠。双转基因小鼠会形成“类人”斑块,为以可控方式研究淀粉样斑块生物学提供了一种机制。用其他方式已实现对标记斑块的成像,但只有磁共振成像(MRI)具有足够的空间和对比度分辨率,能够以非侵入性方式可视化单个斑块。本文描述了在9.4 T磁场下,使用基于绝热脉冲的自旋回波序列,在转基因小鼠体内优化斑块可视化的方法。初步结果表明,自旋回波采集能更准确地反映斑块大小,而T2*加权梯度回波序列反映的是斑块铁含量,而非斑块大小。提供了体内MRI - 体外MRI - 体外组织学之间的相关性。在活体动物中可视化了经组织学验证直径小至50微米的斑块。据我们所知,这项工作首次证明了在不使用造影剂的情况下对单个AD斑块进行非侵入性体内可视化。