Ai. Gulyas et al., The KCI cotransporter, KCC2, is highly expressed in the vicinity of excitatory synapses in the rat hippocampus, EUR J NEURO, 13(12), 2001, pp. 2205-2217
Immunocytochemical visualization of the neuron-specific K+/Cl- cotransporte
r, KCC2, at the cellular and subcellular level revealed an area- and layer-
specific diffuse labelling, and a discrete staining outlining the somata an
d dendrites of some interneurons in all areas of the rat hippocampus. KCC2
was highly expressed in parvalbumin-containing interneurons, as well as in
subsets of calbindin, calretinin and metabotropic glutamate receptor la-imm
unoreactive interneurons. During the first 2 postnatal weeks, an increase o
f KCC2 staining was observed in the molecular layer of the dentate gyrus, c
orrelating temporally with the arrival of entorhinal cortical inputs. Subce
llular localization demonstrated KCC2 in the plasma membranes. Immunoreacti
vity in principal cells was responsible for the diffuse staining found in t
he neuropil. In these cells, KCC2 was detected primarily in dendritic spine
heads, at the origin of spines and, at a much lower level on the somata an
d dendritic shafts. KCC2 expression was considerably higher in the somata a
nd dendrites of interneurons, most notably of parvalbumin-containing cells,
as well as in the thorny excrescences of CA3 pyramidal cells and in the sp
ines of spiny hilar and stratum lucidum interneurons. The data indicate tha
t KCC2 is highly expressed in the vicinity of excitatory inputs in the hipp
ocampus, perhaps in close association with extrasynaptic GABA(A) receptors.
A high level of excitation is known to lead to a simultaneous net influx o
f Na+ and Cl-, as evidenced by dendritic swelling. KCC2 located in the same
microenvironment may provide a Cl- extrusion mechanism to deal with both i
on and water homeostasis in addition to its role in setting the driving for
ce of Cl- currents involved in fast postsynaptic inhibition.