, 2004; Van Esch et al., 2005). While peripheral measures (e.g., respiration) are readily taken, regrettably no direct cortical biomarker is available to monitor the regression or response to treatment in Rett patients. Rett syndrome (RTT) was first characterized in 1983 as “a progressive syndrome of autism, dementia, ataxia, and loss of purposeful hand use in girls,” and was incorporated in the DSM-IV shortly thereafter (Amir et al., 1999; Zoghbi, 2003; Chahrour and Zoghbi, 2007). Since then, a mutation in the gene on the X chromosome encoding the transcriptional modulator protein

MECP2 has been discovered to account for the vast majority Anticancer Compound Library research buy of individuals diagnosed with RTT. Because of its X-linked genetics, RTT mainly affects girls, who are somatic mosaics for normal and mutant MECP2. The spatiotemporal and cellular expression of MECP2 mRNA and protein starts

in basal ganglia by midgestation and extends to cortical neurons in late gestation and postnatally (Amir et al., 1999; Balmer et al., 2003; Armstrong et al., 2003). One key feature of the disorder is that the associated behavioral abnormalities C59 wnt are subtle at first and then progressively deviate from normal development with age. This cannot be explained simply by a pervasive defect in synapse formation (McGraw et al., 2011) but is likely to involve a disrupted process of activity-dependent neuronal circuit refinement with complex outcomes. Mouse models of RTT, considered a gold standard of animal models due to the recapitulation of behavioral and neurobiological symptoms seen in patients, have been critical

for beginning to understand the functional consequences of Mecp2 loss and gain of function. Postnatal loss of Mecp2 from neuronal and non-neuronal cells indicates that discrete features of RTT are associated else with discrete circuits (Gemelli et al., 2006; Fyffe et al., 2008; Ballas et al., 2009; Samaco et al., 2009; Deng et al., 2010; Lioy et al., 2011; Derecki et al., 2012). Importantly, disruption of Mecp2 in all GABA circuits alone may manifest several aspects of Rett Syndrome, including abnormal EEG hyperexcitability, severe respiratory dysrhythmias and early lethality (Chao et al., 2010). Mecp2 deficiency restricted to GABAergic neurons alters Gad1/2 expression and GABA neurotransmitter release, suggesting a decrease of inhibitory function while excitatory drive is grossly unaffected. Instead, global perturbation of Mecp2 expression—closer to the human condition—shifts neocortical excitatory/inhibitory (E/I) balance in favor of inhibition in vitro ( Dani et al., 2005; Nelson et al., 2006; Wood et al., 2009; Wood and Shepherd, 2010), while an enhanced excitation may be found in brainstem circuits ( Shepherd and Katz, 2011).