Bio Engineering Laboratory, Department of Biosystems Science and Engineering, ETH Zurich, 4056 Basel, Switzerland
Blue Brain Project, École polytechnique fédérale de Lausanne, Campus Biotech, 1202 Geneva, Switzerland
Neural Comput. 2024 Jun 7;36(7):1286-1331. doi: 10.1162/neco_a_01672.
In computational neuroscience, multicompartment models are among the most biophysically realistic representations of single neurons. Constructing such models usually involves the use of the patch-clamp technique to record somatic voltage signals under different experimental conditions. The experimental data are then used to fit the many parameters of the model. While patching of the soma is currently the gold-standard approach to build multicompartment models, several studies have also evidenced a richness of dynamics in dendritic and axonal sections. Recording from the soma alone makes it hard to observe and correctly parameterize the activity of nonsomatic compartments. In order to provide a richer set of data as input to multicompartment models, we here investigate the combination of somatic patch-clamp recordings with recordings of high-density microelectrode arrays (HD-MEAs). HD-MEAs enable the observation of extracellular potentials and neural activity of neuronal compartments at subcellular resolution. In this work, we introduce a novel framework to combine patch-clamp and HD-MEA data to construct multicompartment models. We first validate our method on a ground-truth model with known parameters and show that the use of features extracted from extracellular signals, in addition to intracellular ones, yields models enabling better fits than using intracellular features alone. We also demonstrate our procedure using experimental data by constructing cell models from in vitro cell cultures. The proposed multimodal fitting procedure has the potential to augment the modeling efforts of the computational neuroscience community and provide the field with neuronal models that are more realistic and can be better validated.
在计算神经科学中,多腔室模型是最接近单个神经元的生物物理表现形式之一。构建此类模型通常涉及使用膜片钳技术在不同实验条件下记录体电压信号。然后,使用实验数据来拟合模型的许多参数。虽然目前对躯体进行贴片是构建多腔室模型的金标准方法,但已有多项研究表明树突和轴突部分具有丰富的动力学特性。仅对躯体进行记录,很难观察和正确参数化非躯体腔室的活动。为了向多腔室模型提供更丰富的数据集作为输入,我们在这里研究了将体细胞膜片钳记录与高密度微电极阵列(HD-MEAs)记录相结合的方法。HD-MEAs 能够以亚细胞分辨率观察神经元腔室的细胞外电势和神经活动。在这项工作中,我们引入了一种新的框架,将膜片钳和 HD-MEA 数据结合起来构建多腔室模型。我们首先在具有已知参数的真实模型上验证了我们的方法,并表明与仅使用细胞内特征相比,使用从细胞外信号提取的特征(除了细胞内特征)可以产生更好拟合的模型。我们还通过从体外细胞培养物构建细胞模型来演示我们的实验数据处理过程。提出的多模态拟合过程有可能增强计算神经科学领域的建模工作,并为该领域提供更真实、更可验证的神经元模型。