TY - JOUR
T1 - Loss of Mecp2 in substantia nigra dopamine neurons compromises the nigrostriatal pathway
AU - Gantz, Stephanie C.
AU - Ford, Christopher P.
AU - Neve, Kim A.
AU - Williams, John T.
PY - 2011/8/31
Y1 - 2011/8/31
N2 - Mutations in the methyl-CpG-binding protein 2 (MeCP2) result in Rett syndrome (RTT), an X-linked disorder that disrupts neurodevelopment. Girls withRTTexhibit motor deficits similar to those in Parkinson's disease, suggesting defects in the nigrostriatal pathway. This study examined age-dependent changes in dopamine neurons of the substantia nigra (SN) from wild-type, presymptomatic, and symptomatic Mecp2+/- mice. Mecp2+ neurons in the SN in Mecp2+/- mice were indistinguishable in morphology, resting conductance, and dopamine current density from neurons in wild-type mice. However, the capacitance, total dendritic length, and resting conductance of Mecp2- neurons were less than those of Mecp2+ neurons as early as 4 weeks after birth, before overt symptoms. These differences were maintained throughout life. In symptomatic Mecp2+/- mice, the current induced by activation of D2 dopamine autoreceptors was significantly less in Mecp2- neurons than in Mecp2+ neurons, although D2 receptor density was unaltered in Mecp2+/- mice. Electrochemical measurements revealed that significantly less dopamine was released after stimulation of striatum in adult Mecp2+/- mice compared to wild type. The decrease in size and function of Mecp2- neurons observed in adult Mecp2+/- mice was recapitulated in dopamine neurons from symptomatic Mecp2-/y males. These results show that mutation in Mecp2 results in cell-autonomous defects in the SN early in life and throughout adulthood. Ultimately, dysfunction in terminal dopamine release and D2 autoreceptor-dependent currents in dopamine neurons from symptomatic females support the idea that decreased dopamine transmission due to heterogeneous Mecp2 expression contributes to the parkinsonian features of RTT in Mecp2+/- mice.
AB - Mutations in the methyl-CpG-binding protein 2 (MeCP2) result in Rett syndrome (RTT), an X-linked disorder that disrupts neurodevelopment. Girls withRTTexhibit motor deficits similar to those in Parkinson's disease, suggesting defects in the nigrostriatal pathway. This study examined age-dependent changes in dopamine neurons of the substantia nigra (SN) from wild-type, presymptomatic, and symptomatic Mecp2+/- mice. Mecp2+ neurons in the SN in Mecp2+/- mice were indistinguishable in morphology, resting conductance, and dopamine current density from neurons in wild-type mice. However, the capacitance, total dendritic length, and resting conductance of Mecp2- neurons were less than those of Mecp2+ neurons as early as 4 weeks after birth, before overt symptoms. These differences were maintained throughout life. In symptomatic Mecp2+/- mice, the current induced by activation of D2 dopamine autoreceptors was significantly less in Mecp2- neurons than in Mecp2+ neurons, although D2 receptor density was unaltered in Mecp2+/- mice. Electrochemical measurements revealed that significantly less dopamine was released after stimulation of striatum in adult Mecp2+/- mice compared to wild type. The decrease in size and function of Mecp2- neurons observed in adult Mecp2+/- mice was recapitulated in dopamine neurons from symptomatic Mecp2-/y males. These results show that mutation in Mecp2 results in cell-autonomous defects in the SN early in life and throughout adulthood. Ultimately, dysfunction in terminal dopamine release and D2 autoreceptor-dependent currents in dopamine neurons from symptomatic females support the idea that decreased dopamine transmission due to heterogeneous Mecp2 expression contributes to the parkinsonian features of RTT in Mecp2+/- mice.
UR - http://www.scopus.com/inward/record.url?scp=80052358759&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=80052358759&partnerID=8YFLogxK
U2 - 10.1523/JNEUROSCI.0684-11.2011
DO - 10.1523/JNEUROSCI.0684-11.2011
M3 - Article
C2 - 21880923
AN - SCOPUS:80052358759
SN - 0270-6474
VL - 31
SP - 12629
EP - 12637
JO - Journal of Neuroscience
JF - Journal of Neuroscience
IS - 35
ER -