
Dysregulated cortical synaptic plasticity under methyl-CpG binding protein 2 deficiency and its implication in motor impairments
Author(s) -
Weijia Zhang,
Lingling Shi,
Li Zhang
Publication year - 2022
Publication title -
world journal of psychiatry
Language(s) - English
Resource type - Journals
ISSN - 2220-3206
DOI - 10.5498/wjp.v12.i5.673
Subject(s) - rett syndrome , mecp2 , neuroscience , motor cortex , neuroplasticity , neuromodulation , synaptic plasticity , motor coordination , homeostatic plasticity , psychology , medicine , metaplasticity , biology , central nervous system , genetics , phenotype , receptor , stimulation , gene
Caused by the mutation of methyl-CpG binding protein 2 (MeCP2), Rett syndrome leads to a battery of severe neural dysfunctions including the regression of motor coordination and motor learning. Current understanding has revealed the motor cortex as the critical region mediating voluntary movement. In this review article, we will summarize major findings from human patients and animal models regarding the cortical synaptic plasticity under the regulation of MeCP2. We will also discuss how mutation of MeCP2 leads to the disruption of cortical circuitry homeostasis to cause motor deficits. Lastly, potential values of physical exercise and neuromodulation approaches to recover neural plasticity and motor function will be evaluated. All of this evidence may help to accelerate timely diagnosis and effective interventions for Rett syndrome patients.