4.6 Article

Cellular Substrates of Functional Network Integration and Memory in Temporal Lobe Epilepsy

期刊

CEREBRAL CORTEX
卷 32, 期 11, 页码 2424-2436

出版社

OXFORD UNIV PRESS INC
DOI: 10.1093/cercor/bhab349

关键词

action potential kinetics; cellular morphology; connectome; graph theory; resting-state fMRI

资金

  1. Nederlands Epilepsie Fonds [NEF 08-08, 09-09, NEF 14-16]
  2. Dutch Organization for Scientific Research [016.146.086, 198.015]
  3. Society in Science (Branco Weiss Fellowship)
  4. Amsterdam Neuroscience
  5. Dutch Organization for Scientific Research (NWO Veni) [016.Veni.171.017]
  6. Netherlands Organisation for Health Research and Development (ZonMW) [95105006]
  7. European Union [785907]

向作者/读者索取更多资源

This study investigates the cellular substrates of functional network integration in patients with temporal lobe epilepsy (TLE). The findings show that functional network centrality is related to memory performance and cellular integrative properties. These findings provide insights into the focal pathology and network disturbances in TLE.
Temporal lobe epilepsy (TLE) patients are at risk of memory deficits, which have been linked to functional network disturbances, particularly of integration of the default mode network (DMN). However, the cellular substrates of functional network integration are unknown. We leverage a unique cross-scale dataset of drug-resistant TLE patients (n = 31), who underwent pseudo resting-state functional magnetic resonance imaging (fMRI), resting-state magnetoencephalography (MEG) and/or neuropsychological testing before neurosurgery. fMRI and MEG underwent atlas-based connectivity analyses. Functional network centrality of the lateral middle temporal gyrus, part of the DMN, was used as a measure of local network integration. Subsequently, non-pathological cortical tissue from this region was used for single cell morphological and electrophysiological patch-clamp analysis, assessing integration in terms of total dendritic length and action potential rise speed. As could be hypothesized, greater network centrality related to better memory performance. Moreover, greater network centrality correlated with more integrative properties at the cellular level across patients. We conclude that individual differences in cognitively relevant functional network integration of a DMN region are mirrored by differences in cellular integrative properties of this region in TLE patients. These findings connect previously separate scales of investigation, increasing translational insight into focal pathology and large-scale network disturbances in TLE.

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