Department of Anatomy & Neurobiology, Boston University Chobanian & Avedisian School of Medicine, Boston, United States.
Centre de Recerca Matemàtica, Edifici C, Campus Bellaterra, Bellaterra, Spain.
Elife. 2024 Jul 19;12:RP90964. doi: 10.7554/eLife.90964.
Normal aging leads to myelin alterations in the rhesus monkey dorsolateral prefrontal cortex (dlPFC), which are positively correlated with degree of cognitive impairment. It is hypothesized that remyelination with shorter and thinner myelin sheaths partially compensates for myelin degradation, but computational modeling has not yet explored these two phenomena together systematically. Here, we used a two-pronged modeling approach to determine how age-related myelin changes affect a core cognitive function: spatial working memory. First, we built a multicompartment pyramidal neuron model fit to monkey dlPFC empirical data, with an axon including myelinated segments having paranodes, juxtaparanodes, internodes, and tight junctions. This model was used to quantify conduction velocity (CV) changes and action potential (AP) failures after demyelination and subsequent remyelination. Next, we incorporated the single neuron results into a spiking neural network model of working memory. While complete remyelination nearly recovered axonal transmission and network function to unperturbed levels, our models predict that biologically plausible levels of myelin dystrophy, if uncompensated by other factors, can account for substantial working memory impairment with aging. The present computational study unites empirical data from ultrastructure up to behavior during normal aging, and has broader implications for many demyelinating conditions, such as multiple sclerosis or schizophrenia.
正常衰老导致恒河猴背外侧前额叶皮层(dlPFC)的髓鞘改变,与认知障碍的程度呈正相关。据推测,较短和较薄的髓鞘的再髓鞘化部分补偿了髓鞘的降解,但计算模型尚未系统地探索这两种现象。在这里,我们使用了一种双管齐下的建模方法来确定与年龄相关的髓鞘变化如何影响核心认知功能:空间工作记忆。首先,我们构建了一个符合猴子 dlPFC 经验数据的多腔锥体神经元模型,该模型的轴突包括具有髓鞘节段的有髓段,具有节间段、毗邻节段、节间段和紧密连接。该模型用于量化脱髓鞘和随后再髓鞘化后的传导速度(CV)变化和动作电位(AP)故障。接下来,我们将单个神经元的结果纳入工作记忆的尖峰神经网络模型中。虽然完全再髓鞘化几乎恢复了未受干扰水平的轴突传输和网络功能,但我们的模型预测,如果没有其他因素的补偿,生物上合理的髓鞘营养不良水平可能会导致随着年龄增长而出现大量的工作记忆障碍。本计算研究将正常衰老过程中的超微结构直至行为的经验数据结合在一起,对许多脱髓鞘疾病具有更广泛的意义,如多发性硬化症或精神分裂症。