TY - JOUR
T1 - Climbing Fiber Activation of EAAT4 Transporters and Kainate Receptors in Cerebellar Purkinje Cells
AU - Huang, Yanhua H.
AU - Dykes-Hoberg, Margaret
AU - Tanaka, Kohichi
AU - Rothstein, Jeffrey D.
AU - Bergles, Dwight E.
PY - 2004/1/7
Y1 - 2004/1/7
N2 - Cerebellar Purkinje cells (PCs) express two glutamate transporters, EAAC1 (EAAT3) and EAAT4; however, their relative contribution to the uptake of glutamate at synapses is not known. We found that glutamate transporter currents recorded at climbing fiber (CF)-PC synapses are absent in mice lacking EAAT4 but unchanged in mice lacking EAAC1, indicating that EAAT4 is preferentially involved in clearing glutamate from CF synapses. However, comparison of CF synaptic currents between wild-type and transporter knock-out mice revealed that ionotropic glutamate receptors are responsible for >40% of the current previously attributed to transporters, indicating that PCs remove <10% of the glutamate released by the CF. The receptors responsible for the nontransporter component accounted for 5% of the CF EPSC, had a slower time course and lower occupancy than AMPA receptors at CF synapses, and exhibited pharmacological properties consistent with kainate receptors. In GluR5 knock-out mice, this current was dramatically reduced, indicating that CF excitation of PCs involves two distinct classes of ionotropic glutamate receptors, AMPA receptors and GluR5-containing kainate receptors.
AB - Cerebellar Purkinje cells (PCs) express two glutamate transporters, EAAC1 (EAAT3) and EAAT4; however, their relative contribution to the uptake of glutamate at synapses is not known. We found that glutamate transporter currents recorded at climbing fiber (CF)-PC synapses are absent in mice lacking EAAT4 but unchanged in mice lacking EAAC1, indicating that EAAT4 is preferentially involved in clearing glutamate from CF synapses. However, comparison of CF synaptic currents between wild-type and transporter knock-out mice revealed that ionotropic glutamate receptors are responsible for >40% of the current previously attributed to transporters, indicating that PCs remove <10% of the glutamate released by the CF. The receptors responsible for the nontransporter component accounted for 5% of the CF EPSC, had a slower time course and lower occupancy than AMPA receptors at CF synapses, and exhibited pharmacological properties consistent with kainate receptors. In GluR5 knock-out mice, this current was dramatically reduced, indicating that CF excitation of PCs involves two distinct classes of ionotropic glutamate receptors, AMPA receptors and GluR5-containing kainate receptors.
KW - Cerebellum
KW - EAAC1
KW - EAAT4
KW - EPSC
KW - GluR5
KW - Glutamate transporter
KW - Kainate receptor
KW - Purkinje neuron
UR - http://www.scopus.com/inward/record.url?scp=0842301342&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0842301342&partnerID=8YFLogxK
U2 - 10.1523/JNEUROSCI.4473-03.2004
DO - 10.1523/JNEUROSCI.4473-03.2004
M3 - Article
C2 - 14715943
AN - SCOPUS:0842301342
SN - 0270-6474
VL - 24
SP - 103
EP - 111
JO - Journal of Neuroscience
JF - Journal of Neuroscience
IS - 1
ER -