School of Psychology, University of Nottingham, Nottingham, NG7 2RD, United Kingdom
J Neurosci. 2022 Feb 23;42(8):1417-1435. doi: 10.1523/JNEUROSCI.1487-21.2021. Epub 2021 Dec 10.
The striatum's complex microcircuit is made by connections within and between its D1- and D2-receptor expressing projection neurons and at least five species of interneuron. Precise knowledge of this circuit is likely essential to understanding striatum's functional roles and its dysfunction in a wide range of movement and cognitive disorders. We introduce here a Bayesian approach to mapping neuron connectivity using intracellular recording data, which lets us simultaneously evaluate the probability of connection between neuron types, the strength of evidence for it, and its dependence on distance. Using it to synthesize a complete map of the mouse striatum, we find strong evidence for two asymmetries: a selective asymmetry of projection neuron connections, with D2 neurons connecting twice as densely to other projection neurons than do D1 neurons, but neither subtype preferentially connecting to another; and a length-scale asymmetry, with interneuron connection probabilities remaining non-negligible at more than twice the distance of projection neuron connections. We further show that our Bayesian approach can evaluate evidence for wiring changes, using data from the developing striatum and a mouse model of Huntington's disease. By quantifying the uncertainty in our knowledge of the microcircuit, our approach reveals a wide range of potential striatal wiring diagrams consistent with current data. To properly understand a neuronal circuit's function, it is important to have an accurate picture of the rate of connection between individual neurons and how this rate changes with the distance separating pairs of neurons. We present a Bayesian method for extracting this information from experimental data and apply it to the mouse striatum, a subcortical structure involved in learning and decision-making, which is made up of a variety of different projection neurons and interneurons. Our resulting statistical map reveals not just the most robust estimates of the probability of connection between neuron types, but also the strength of evidence for them, and their dependence on distance.
纹状体的复杂微电路是由其 D1- 和 D2- 受体表达投射神经元和至少五种类型的中间神经元之间的连接形成的。精确了解该电路对于理解纹状体的功能作用及其在广泛的运动和认知障碍中的功能障碍可能是至关重要的。我们在这里介绍了一种使用细胞内记录数据来绘制神经元连接的贝叶斯方法,该方法使我们能够同时评估神经元类型之间连接的可能性、其证据强度以及其对距离的依赖性。我们使用它来合成完整的小鼠纹状体图谱,发现了两个明显的不对称性:投射神经元连接的选择性不对称性,D2 神经元与其他投射神经元的连接密度是 D1 神经元的两倍,但没有一种亚型优先与另一种亚型连接;以及长度尺度不对称性,中间神经元的连接概率在两倍以上的投射神经元连接距离处仍然不可忽略。我们进一步表明,我们的贝叶斯方法可以使用来自发育中的纹状体和亨廷顿病小鼠模型的数据来评估连接变化的证据。通过量化我们对微电路的知识的不确定性,我们的方法揭示了与当前数据一致的广泛的潜在纹状体布线图。为了正确理解神经元电路的功能,了解个体神经元之间连接的速率以及这种速率如何随分离对神经元的距离而变化是很重要的。我们提出了一种从实验数据中提取这些信息的贝叶斯方法,并将其应用于小鼠纹状体,这是一种涉及学习和决策的皮层下结构,由各种不同的投射神经元和中间神经元组成。我们的统计图谱不仅揭示了神经元类型之间连接的最可靠估计,还揭示了它们的证据强度及其对距离的依赖性。