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Premature expression of KCC2 in embryonic mice perturbs neural development by an ion transport‐independent mechanism
Author(s) -
Horn Zachi,
Ringstedt Thomas,
Blaesse Peter,
Kaila Kai,
Herlenius Eric
Publication year - 2010
Publication title -
european journal of neuroscience
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.346
H-Index - 206
eISSN - 1460-9568
pISSN - 0953-816X
DOI - 10.1111/j.1460-9568.2010.07258.x
Subject(s) - neural tube , neural crest , microbiology and biotechnology , biology , embryo , embryonic stem cell , neural plate , cytoskeleton , intracellular , neuroepithelial cell , neurulation , embryogenesis , neural stem cell , cell , genetics , stem cell , gene , gastrulation
During neuronal maturation, the neuron‐specific K–Cl co‐transporter KCC2 lowers the intracellular chloride and thereby renders GABAergic transmission hyperpolarizing. Independently of its role as a co‐transporter, KCC2 plays a crucial role in the maturation of dendritic spines, most probably via an interaction with the cytoskeleton‐associated protein 4.1N. In this study, we show that neural‐specific overexpression of KCC2 impairs the development of the neural tube‐ and neural crest‐related structures in mouse embryos. At early stages (E9.5–11.5), the transgenic embryos had a thinner neural tube and abnormal body curvature. They displayed a reduced neuronal differentiation and altered neural crest cell pattern. At later stages (E11.5–15.5), the transgenic embryos had smaller brain structures and a distinctive cleft palate. Similar results were obtained using overexpression of a transport‐inactive N‐terminal‐deleted variant of KCC2, implying that the effects were not dependent on KCC2′s role as a K–Cl co‐transporter. Interestingly, the neural tube of transgenic embryos had an aberrant cytoplasmic distribution of 4.1N and actin. This was corroborated in a neural stem cell line with ectopic expression of KCC2. Embryo phenotype and cell morphology were unaffected by a mutated variant of KCC2 which is unable to bind 4.1N. These results point to a role of KCC2 in neuronal differentiation and migration during early development mediated by its direct structural interactions with the neuronal cytoskeleton.