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An ion transport-independent role for the cation-chloride cotransporter KCC2 in dendritic spinogenesis in vivo.

Authors: Fiumelli, H  Briner, A  Puskarjov, M  Blaesse, P  Belem, BJ  Dayer, AG  Kaila, K  Martin, JL  Vutskits, L 
Citation: Fiumelli H, etal., Cereb Cortex. 2013 Feb;23(2):378-88. doi: 10.1093/cercor/bhs027. Epub 2012 Feb 17.
Pubmed: (View Article at PubMed) PMID:22345354
DOI: Full-text: DOI:10.1093/cercor/bhs027

The neuron-specific K-Cl cotransporter, KCC2, is highly expressed in the vicinity of excitatory synapses in pyramidal neurons, and recent in vitro data suggest that this protein plays a role in the development of dendritic spines. The in vivo relevance of these observations is, however, unknown. Using in utero electroporation combined with post hoc iontophoretic injection of Lucifer Yellow, we show that premature expression of KCC2 induces a highly significant and permanent increase in dendritic spine density of layer 2/3 pyramidal neurons in the somatosensory cortex. Whole-cell recordings revealed that this increased spine density is correlated with an enhanced spontaneous excitatory activity in KCC2-transfected neurons. Precocious expression of the N-terminal deleted form of KCC2, which lacks the chloride transporter function, also increased spine density. In contrast, no effect on spine density was observed following in utero electroporation of a point mutant of KCC2 (KCC2-C568A) where both the cotransporter function and the interaction with the cytoskeleton are disrupted. Transfection of the C-terminal domain of KCC2, a region involved in the interaction with the dendritic cytoskeleton, also increased spine density. Collectively, these results demonstrate a role for KCC2 in excitatory synaptogenesis in vivo through a mechanism that is independent of its ion transport function.


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CRRD Object Information
CRRD ID: 10449516
Created: 2016-01-09
Species: All species
Last Modified: 2016-01-09
Status: ACTIVE


RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.