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[P2.39]: Dendritic inhibition defects lead to epilepsy in Lhx6 hypomorphic mutant mice
Author(s) -
Neves G.,
Liodis P.,
Achimastou A.,
Roalfe G.,
Shah M.,
Pachnis V.
Publication year - 2010
Publication title -
international journal of developmental neuroscience
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.761
H-Index - 88
eISSN - 1873-474X
pISSN - 0736-5748
DOI - 10.1016/j.ijdevneu.2010.07.169
Subject(s) - library science , political science , computer science
used transgenic mice expressing activated human Val12 Ha-Ras selectively in neurons resulting in enhanced cortical synaptic longterm potentiation (Heumann et al, 2000; Arendt et al., 2004). The crossbreeding of heterozygous MeCP2+/−-females with transgenic synRas-males resulted in a dramatically increased lethality. Furthermore, in contrast to heterozygous MeCP−/y-males double transgenic synRas/MeCP−/y-males did not survive beyond postnatal day 28. Female synRas/MeCP2+/−-mice had an almost normal lifespan. However, these double transgenic female mice developed an enhanced anxiety-like behaviour in the elevated plus maze comparable to that of the strongly affected MeCP2−/y-males. We conclude that activation of the Ras/MAPkinase pathway in neurons accelerated the adverse RTT phenotype and therefore Ras may serve as a target for therapeutical intervention. References: