The KCI cotransporter, KCC2, is highly expressed in the vicinity of excitatory synapses in the rat hippocampus

Citation
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
Citations number
69
Categorie Soggetti
Neurosciences & Behavoir
Journal title
EUROPEAN JOURNAL OF NEUROSCIENCE
ISSN journal
0953816X → ACNP
Volume
13
Issue
12
Year of publication
2001
Pages
2205 - 2217
Database
ISI
SICI code
0953-816X(200106)13:12<2205:TKCKIH>2.0.ZU;2-0
Abstract
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.