Brain Structures in a Human Embryo Imaged with MR Microscopy.

Kazuki Kunieda, Kazuyuki Makihara, Shigehito Yamada, Masayuki Yamaguchi, Takashi Nakamura, Yasuhiko Terada
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Abstract

Purpose: To delineate brain microstructures in human embryos during the formation of the various major primordia by MR microscopy, with different contrasts appropriate for each target.

Methods: We focused mainly on the internal structures in the cerebral cortex and the accessory nerves of the brain. To find appropriate sequence parameters, we measured nuclear magnetic resonance (NMR) parameters and created kernel density plots of T1 and T2 values. We performed T1-weighted gradient echo imaging with parameters similar to those used in the previous studies. We performed T2*-weighted gradient echo imaging to delineate the target structures with the appropriate sequence parameters according to the NMR parameter and flip angle measurements. We also performed high-resolution imaging with both T1- and T2*-weighted sequences.

Results: T1, T2, and T2* values of the target tissues were positively correlated and shorter than those of the surrounding tissues. In T1-weighted images with a voxel size of (30 µm)3 and (20 µm)3, various organs and tissues and the agarose gel were differentiated as in previous studies, and the structure of approximately 40 µm in size was depicted, but the detailed structures within the cerebral cortex and the accessory nerves were not delineated. In T2*-weighted images with a voxel size of (30 µm)3, the layered structure within the cerebral cortex and the accessory nerves were clearly visualized. Overall, T1-weighted images provided more information than T2*-weighted images, but important internal brain structures of interest were visible only in T2*-weighted images. Therefore, it is essential to perform MR microscopy with different contrasts.

Conclusion: We have visualized brain structures in a human embryo that had not previously been delineated by MR microscopy. We discussed pulse sequences appropriate for the structures of interest. This methodology would provide a way to visualize crucial embryological information about the anatomical structure of human embryos.

利用核磁共振显微镜成像的人类胚胎大脑结构。
目的:通过磁共振显微镜描绘人类胚胎在各主要原基形成过程中的大脑微观结构,并针对每个目标采用不同的对比度:我们主要关注大脑皮层和大脑附属神经的内部结构。为了找到合适的序列参数,我们测量了核磁共振(NMR)参数,并绘制了 T1 和 T2 值的核密度图。我们进行了 T1 加权梯度回波成像,其参数与之前研究中使用的参数相似。我们进行了 T2* 加权梯度回波成像,根据 NMR 参数和翻转角测量结果,使用适当的序列参数来划分目标结构。我们还使用 T1 和 T2* 加权序列进行了高分辨率成像:结果:靶组织的 T1、T2 和 T2* 值呈正相关,且比周围组织短。在体素大小为(30 微米)3 和(20 微米)3 的 T1 加权图像中,各种器官和组织以及琼脂糖凝胶与之前的研究一样被区分开来,约 40 微米大小的结构被描绘出来,但大脑皮层和附属神经内部的详细结构没有被勾勒出来。在体素大小为(30 微米)3 的 T2*加权图像中,大脑皮层和附属神经的分层结构清晰可见。总体而言,T1 加权图像比 T2* 加权图像提供的信息更多,但重要的脑内部结构只有在 T2* 加权图像中才能看到。因此,必须使用不同的对比度进行磁共振显微镜检查:结论:我们在人类胚胎中观察到了以前从未用磁共振显微镜描绘过的大脑结构。我们讨论了适合相关结构的脉冲序列。这种方法将为可视化人类胚胎解剖结构的重要胚胎学信息提供一种途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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