Reduced oriens-lacunosum/moleculare cell model identifies biophysical current balances for in vivo theta frequency spiking resonance.

IF 3.4 3区 医学 Q2 NEUROSCIENCES Frontiers in Neural Circuits Pub Date : 2023-02-03 eCollection Date: 2023-01-01 DOI:10.3389/fncir.2023.1076761
Zhenyang Sun, David Crompton, Milad Lankarany, Frances K Skinner
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Abstract

Conductance-based models have played an important role in the development of modern neuroscience. These mathematical models are powerful "tools" that enable theoretical explorations in experimentally untenable situations, and can lead to the development of novel hypotheses and predictions. With advances in cell imaging and computational power, multi-compartment models with morphological accuracy are becoming common practice. However, as more biological details are added, they make extensive explorations and analyses more challenging largely due to their huge computational expense. Here, we focus on oriens-lacunosum/moleculare (OLM) cell models. OLM cells can contribute to functionally relevant theta rhythms in the hippocampus by virtue of their ability to express spiking resonance at theta frequencies, but what characteristics underlie this is far from clear. We converted a previously developed detailed multi-compartment OLM cell model into a reduced single compartment model that retained biophysical fidelity with its underlying ion currents. We showed that the reduced OLM cell model can capture complex output that includes spiking resonance in in vivo-like scenarios as previously obtained with the multi-compartment model. Using the reduced model, we were able to greatly expand our in vivo-like scenarios. Applying spike-triggered average analyses, we were able to to determine that it is a combination of hyperpolarization-activated cation and muscarinic type potassium currents that specifically allow OLM cells to exhibit spiking resonance at theta frequencies. Further, we developed a robust Kalman Filtering (KF) method to estimate parameters of the reduced model in real-time. We showed that it may be possible to directly estimate conductance parameters from experiments since this KF method can reliably extract parameter values from model voltage recordings. Overall, our work showcases how the contribution of cellular biophysical current details could be determined and assessed for spiking resonance. As well, our work shows that it may be possible to directly extract these parameters from current clamp voltage recordings.

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缩小的oriens-lacunosum/moleculare细胞模型确定了体内θ频率尖峰共振的生物物理电流平衡。
基于电导的模型在现代神经科学的发展中发挥了重要作用。这些数学模型是强大的 "工具",能在实验无法成立的情况下进行理论探索,并能提出新的假设和预测。随着细胞成像技术和计算能力的进步,具有形态学准确性的多室模型已成为一种普遍做法。然而,随着更多生物细节的加入,它们使广泛的探索和分析更具挑战性,这主要是由于其巨大的计算成本。在此,我们将重点放在oriens-lacunosum/moleculare(OLM)细胞模型上。OLM细胞能在θ频率上表达尖峰共振,因此能促进海马中与功能相关的θ节律,但究竟是什么特征导致了这种情况,目前还不清楚。我们将以前开发的一个详细的多室 OLM 细胞模型转换成了一个简化的单室模型,该模型保留了其基本离子电流的生物物理保真度。我们的研究表明,缩小的 OLM 细胞模型可以捕捉到复杂的输出,包括在类似活体场景中的尖峰共振,这与之前使用多室模型获得的结果相同。利用简化模型,我们能够大大扩展我们的类活体情景。通过尖峰触发平均分析,我们确定是超极化激活阳离子和毒蕈碱型钾电流的组合使 OLM 细胞在θ 频率表现出尖峰共振。此外,我们还开发了一种稳健的卡尔曼滤波(KF)方法,用于实时估计简化模型的参数。我们的研究表明,由于这种 KF 方法能从模型电压记录中可靠地提取参数值,因此有可能直接从实验中估计电导参数。总之,我们的工作展示了如何确定和评估细胞生物物理电流细节对尖峰共振的贡献。此外,我们的工作还表明,有可能直接从电流钳电压记录中提取这些参数。
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来源期刊
CiteScore
6.00
自引率
5.70%
发文量
135
审稿时长
4-8 weeks
期刊介绍: Frontiers in Neural Circuits publishes rigorously peer-reviewed research on the emergent properties of neural circuits - the elementary modules of the brain. Specialty Chief Editors Takao K. Hensch and Edward Ruthazer at Harvard University and McGill University respectively, are supported by an outstanding Editorial Board of international experts. This multidisciplinary open-access journal is at the forefront of disseminating and communicating scientific knowledge and impactful discoveries to researchers, academics and the public worldwide. Frontiers in Neural Circuits launched in 2011 with great success and remains a "central watering hole" for research in neural circuits, serving the community worldwide to share data, ideas and inspiration. Articles revealing the anatomy, physiology, development or function of any neural circuitry in any species (from sponges to humans) are welcome. Our common thread seeks the computational strategies used by different circuits to link their structure with function (perceptual, motor, or internal), the general rules by which they operate, and how their particular designs lead to the emergence of complex properties and behaviors. Submissions focused on synaptic, cellular and connectivity principles in neural microcircuits using multidisciplinary approaches, especially newer molecular, developmental and genetic tools, are encouraged. Studies with an evolutionary perspective to better understand how circuit design and capabilities evolved to produce progressively more complex properties and behaviors are especially welcome. The journal is further interested in research revealing how plasticity shapes the structural and functional architecture of neural circuits.
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