Tucciarone Jason, Chuang Kai-Hsiang, Dodd Steven J, Silva Afonso, Pelled Galit, Koretsky Alan P
Laboratory of Functional and Molecular Imaging, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD 20892-1065, USA.
Neuroimage. 2009 Feb 1;44(3):923-31. doi: 10.1016/j.neuroimage.2008.07.036. Epub 2008 Jul 29.
Information about layer specific connections in the brain comes mainly from classical neuronal tracers that rely on histology. Manganese Enhanced MRI (MEMRI) has mapped connectivity along a number of brain pathways in several animal models. It is not clear at what level of specificity neuronal connectivity measured using MEMRI tracing can resolve. The goal of this work was to determine if neural tracing using MEMRI could distinguish layer inputs of major pathways of the cortex. To accomplish this, tracing was performed between hemispheres of the somatosensory (S1) cortex and between the thalamus and S1 cortex. T(1) mapping and T(1) weighted pulse sequences detected layer specific tracing after local injection of MnCl(2). Approximately 12 h following injections into S1 cortex, maximal T(1) reductions were observed at 0.6+/-0.07 and 1.1+/-0.12 mm from the brain surface in the contralateral S1. These distances correspond to the positions of layer 3 and 5 consistent with the known callosal inputs along this pathway. Four to six hours following injection of MnCl(2) into the thalamus there were maximal T(1) reductions between 0.7+/-0.08 and 0.8+/-0.08 mm from the surface of the brain, which corresponds to layer 4. This is consistent with terminations of the known thalamocortical projections. In order to observe the first synapse projection, it was critical to perform MRI at the right time after injections to detect layer specificity with MEMRI. At later time points, tracing through the cortical network led to more uniform contrast throughout the cortex due to its complex neuronal connections. These results are consistent with well established neuronal pathways within the somatosensory cortex and demonstrate that layer specific somatosensory connections can be detected in vivo using MEMRI.
关于大脑中特定层连接的信息主要来自依赖组织学的经典神经元示踪剂。锰增强磁共振成像(MEMRI)已在多种动物模型中描绘了沿多条脑通路的连接性。目前尚不清楚使用MEMRI追踪测量的神经元连接性在何种特异性水平上能够分辨。这项工作的目标是确定使用MEMRI进行神经追踪是否能够区分皮质主要通路的层输入。为了实现这一目标,在体感(S1)皮质的半球之间以及丘脑与S1皮质之间进行了追踪。在局部注射MnCl₂后,通过T(1)映射和T(1)加权脉冲序列检测到层特异性追踪。在向S1皮质注射后约12小时,在对侧S1中距脑表面0.6±0.07和1.1±0.12毫米处观察到最大T(1)降低。这些距离与第3层和第5层的位置相对应,与沿该通路已知的胼胝体输入一致。在向丘脑注射MnCl₂后4至6小时,在距脑表面0.7±0.08和0.8±0.08毫米之间观察到最大T(1)降低,这对应于第4层。这与已知的丘脑皮质投射的终止一致。为了观察第一个突触投射,在注射后在合适的时间进行MRI以检测MEMRI的层特异性至关重要。在更晚的时间点,由于其复杂的神经元连接,通过皮质网络的追踪导致整个皮质的对比度更加均匀。这些结果与体感皮质内已确立的神经元通路一致,并表明使用MEMRI可以在体内检测到层特异性体感连接。