Badea Alexandra, Nicholls Peter J, Johnson G Allan, Wetsel William C
Center for In Vivo Microscopy, Box 3302, Duke University Medical Center, Durham, NC 27710, USA.
Neuroimage. 2007 Feb 15;34(4):1363-74. doi: 10.1016/j.neuroimage.2006.09.053. Epub 2006 Dec 20.
The reeler mouse (Reln) has been proposed as a neurodevelopmental model for certain neurological and psychiatric conditions and has been studied by qualitative histochemistry and electron microscopy. Using magnetic resonance microscopy (MRM), we have quantitated for the first time the neuromorphology of Reln mice at a resolution of 21.5 microm. The neuroanatomical phenotypes of heterozygous and homozygous mutant Reln mice were compared to those of wild type (WT) littermates using morphometry and texture analysis. The cortical, hippocampal, and cerebellar phenotypes of the heterozygous and homozygous mutant Reln mice were confirmed, and new features were revealed. The Reln(rl/rl) mice possessed a smaller brain, and both Reln(rl/+) and Reln(rl/rl) mice had increased ventricles compared to WT controls. Shape differences were found between WT and Reln(rl/rl) brains, specifically in cerebellum, olfactory bulbs, dorsomedial frontal and parietal cortex, certain regions of temporal and occipital lobes, as well as in the lateral ventricles and ventral hippocampus. These findings suggest that certain brain regions may be more severely impacted by the Reln mutation than others. Gadolinium-based active staining demonstrated that layers of the hippocampus were disorganized in Reln(rl/rl) mice and differences in thickness of these layers were identified between WT and Reln(rl/rl) mice. The intensity distributions characteristic to the dorsal, middle, and ventral hippocampus were altered in the Reln(rl/rl), especially in the ventral hippocampus. These differences were quantified using skewness and modeling the intensity distributions with a Gaussian mixture. Our results suggest that structural features of Reln(rl/rl) brain most closely phenocopy those of patients with Norman-Roberts lissencephaly.
摇椅鼠(Reln)已被提议作为某些神经和精神疾病的神经发育模型,并已通过定性组织化学和电子显微镜进行研究。使用磁共振显微镜(MRM),我们首次以21.5微米的分辨率对Reln小鼠的神经形态进行了定量分析。使用形态计量学和纹理分析,将杂合子和纯合子突变型Reln小鼠的神经解剖学表型与野生型(WT)同窝小鼠进行了比较。杂合子和纯合子突变型Reln小鼠的皮质、海马和小脑表型得到了证实,并揭示了新的特征。Reln(rl/rl)小鼠的脑体积较小,与WT对照相比,Reln(rl/+)和Reln(rl/rl)小鼠的脑室均增大。在WT和Reln(rl/rl)大脑之间发现了形状差异,特别是在小脑、嗅球、背内侧额叶和顶叶皮质、颞叶和枕叶的某些区域,以及侧脑室和腹侧海马。这些发现表明,某些脑区可能比其他脑区更容易受到Reln突变的严重影响。基于钆的活性染色表明,Reln(rl/rl)小鼠海马层结构紊乱,WT和Reln(rl/rl)小鼠之间这些层的厚度存在差异。Reln(rl/rl)小鼠背侧、中间和腹侧海马的强度分布特征发生了改变,尤其是在腹侧海马。使用偏度和高斯混合模型对强度分布进行建模,对这些差异进行了量化。我们的结果表明,Reln(rl/rl)大脑的结构特征与诺曼-罗伯茨无脑回畸形患者的特征最为相似。