Center for Information and Neural Networks (CiNet), National Institute of Information and Communications Technology and Osaka University, Suita 565-0871, Japan.
Graduate School of Frontier Biosciences, Osaka University, Suita 565-0871, Japan.
Proc Natl Acad Sci U S A. 2018 Nov 27;115(48):12289-12294. doi: 10.1073/pnas.1804741115. Epub 2018 Nov 14.
Stereopsis is a fundamental visual function that has been studied extensively. However, it is not clear why depth discrimination (stereoacuity) varies more significantly among people than other modalities. Previous studies have reported the involvement of both dorsal and ventral visual areas in stereopsis, implying that not only neural computations in cortical areas but also the anatomical properties of white matter tracts connecting those areas can impact stereopsis. Here, we studied how human stereoacuity relates to white matter properties by combining psychophysics, diffusion MRI (dMRI), and quantitative MRI (qMRI). We performed a psychophysical experiment to measure stereoacuity and, in the same participants, we analyzed the microstructural properties of visual white matter tracts on the basis of two independent measurements, dMRI (fractional anisotropy, FA) and qMRI (macromolecular tissue volume; MTV). Microstructural properties along the right vertical occipital fasciculus (VOF), a major tract connecting dorsal and ventral visual areas, were highly correlated with measures of stereoacuity. This result was consistent for both FA and MTV, suggesting that the behavioral-structural relationship reflects differences in neural tissue density, rather than differences in the morphological configuration of fibers. fMRI confirmed that binocular disparity stimuli activated the dorsal and ventral visual regions near VOF endpoints. No other occipital tracts explained the variance in stereoacuity. In addition, the VOF properties were not associated with differences in performance on a different psychophysical task (contrast detection). These series of experiments suggest that stereoscopic depth discrimination performance is, at least in part, constrained by dorso-ventral communication through the VOF.
立体视是一种已被广泛研究的基本视觉功能。然而,为什么深度辨别(立体敏锐度)在人与人之间的变化比其他模态更为显著,目前还不清楚。先前的研究报告称,背侧和腹侧视觉区域都参与了立体视,这意味着不仅皮层区域的神经计算,还有连接这些区域的白质束的解剖特性也会影响立体视。在这里,我们通过结合心理物理学、扩散 MRI(dMRI)和定量 MRI(qMRI)来研究人类立体敏锐度与白质特性之间的关系。我们进行了一项心理物理学实验来测量立体敏锐度,并且在同一组参与者中,我们基于两种独立的测量方法(dMRI(各向异性分数,FA)和 qMRI(大分子组织体积;MTV))分析了视觉白质束的微观结构特性。沿右侧垂直枕状束(VOF)的微观结构特性与立体敏锐度的测量高度相关,该束是连接背侧和腹侧视觉区域的主要束。FA 和 MTV 的结果都一致,这表明行为-结构关系反映了神经组织密度的差异,而不是纤维形态结构的差异。fMRI 证实双眼视差刺激激活了 VOF 终点附近的背侧和腹侧视觉区域。没有其他枕叶束可以解释立体敏锐度的变化。此外,VOF 的特性与不同心理物理任务(对比度检测)的性能差异无关。这一系列实验表明,立体深度辨别性能至少部分受到 VOF 中背腹通讯的限制。