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Updated: Sep 15, 2025

Isolation of Region-specific Microglia from One Adult Mouse Brain Hemisphere for Deep Single-cell RNA Sequencing
Published on: December 3, 2019
SnRNA-seq Interprets Mechanisms by which Three Glial Cell Types Influence Myelin Regeneration in Adult Drug-Resistant
Lu Wang1, Jia-Qi Ma1, Yong-Qian Bian2
1Department of Neurosurgery, Tangdu Hospital, Airforce Military Medical University, Xi'an, Shaanxi, China.
Abstract:
Myelin regeneration has been shown in previous studies to ameliorate varying degrees of cognitive impairment in patients with neurodegenerative disorders such as epilepsy. The problem of myelin regeneration in adults with drug-resistant status epilepticus is a major key to the difficulty of treating cognitive impairment in adults with drug-resistant epilepsy (DRE). The purpose of this study is to provide a molecular map of myelin-related molecules under the cognitive deficits seen in DRE. We used a lamotrigine-pentylenetetrazol-resistant epilepsy mouse model and verified the cognitive problems and myelin changes using a water maze and conventional molecular biology techniques. We then analyzed the OLs in the hippocampus of the mice and the effect on myelin using sn RNA-seq technology. We found that the problem of cognitive impairment in drug-resistant epileptic mice is due to altered myelin plasticity. OL maturation induces pathological myelin regeneration which ultimately leads to cognitive impairment. The three glial cell types are closely related to the occurrence of myelin regeneration and jointly promote pathological myelin regeneration. Our study revealed the presence of myelin regeneration in DRE. All of this evidence suggests that normal myelin regeneration contributes to cognitive impairment improvement, but pathological myelin regeneration impairs cognition.
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