TY - JOUR
T1 - Measurement of glial transport currents in microcultures
T2 - Application to excitatory neurotransmission
AU - Mennerick, Steven
AU - Zorumski, Charles F.
N1 - Funding Information:
The authors thank P. Dhond, N. C. Danbolt, and K. Isenberg for collaborating in the immunohistochemistry shown in Fig. 1, and thank A. Benz for help in development and maintenance of the microcultures. Work in the authors' laboratory is supported by a McDonnell fellowship (S.M.), by NIMH Research Scientist Development Award MH00964, grants MH45493 and AGl1355, and a fellowship from the Bantly Foundation.
Funding Information:
This work was supported by the Wellcome Trust, M.R.C., and the European Community (CT95-571).
PY - 1998
Y1 - 1998
N2 - We have found microcultures of neurons and astrocytes to provide a useful experimental preparation for studying the role of glutamate transporters in synaptic physiology. The preparation balances experimental control over a number of important variables with an environment that mimics many fundamental features of synapses in situ. Several avenues exist for further use of microcultures in the study of transporters. Although our studies have focused primarily on the role of transporters in the new milliseconds subsequent to individual synaptic events, it is likely that microcultures may prove useful for studying slower effects of transporters in maintaining or modulating tonic ambient glutamate levels. Another avenue for further research is to understand which of the several cloned glutamate transporters may be responsible for the observed physiological effects of transporters in microcultures. Finally, because a number of neuronal transmitter phenotypes have been shown to survive in the microculture environment, it may be possible to extend studies of transmitter transport to other transmitter phenotypes and to other nervous system regions.
AB - We have found microcultures of neurons and astrocytes to provide a useful experimental preparation for studying the role of glutamate transporters in synaptic physiology. The preparation balances experimental control over a number of important variables with an environment that mimics many fundamental features of synapses in situ. Several avenues exist for further use of microcultures in the study of transporters. Although our studies have focused primarily on the role of transporters in the new milliseconds subsequent to individual synaptic events, it is likely that microcultures may prove useful for studying slower effects of transporters in maintaining or modulating tonic ambient glutamate levels. Another avenue for further research is to understand which of the several cloned glutamate transporters may be responsible for the observed physiological effects of transporters in microcultures. Finally, because a number of neuronal transmitter phenotypes have been shown to survive in the microculture environment, it may be possible to extend studies of transmitter transport to other transmitter phenotypes and to other nervous system regions.
UR - http://www.scopus.com/inward/record.url?scp=0031718931&partnerID=8YFLogxK
U2 - 10.1016/S0076-6879(98)96045-1
DO - 10.1016/S0076-6879(98)96045-1
M3 - Article
C2 - 9779479
AN - SCOPUS:0031718931
SN - 0076-6879
VL - 296
SP - 632
EP - 645
JO - Methods in enzymology
JF - Methods in enzymology
ER -