Kp. Lehre et Nc. Danbolt, THE NUMBER OF GLUTAMATE TRANSPORTER SUBTYPE MOLECULES AT GLUTAMATERGIC SYNAPSES - CHEMICAL AND STEREOLOGICAL QUANTIFICATION IN YOUNG-ADULT RAT-BRAIN, The Journal of neuroscience, 18(21), 1998, pp. 8751-8757
The role of transporters in shaping the glutamate concentration in the
extracellular space after synaptic release is controversial because o
f their slow cycling and because diffusion alone gives a rapid removal
. The transporter densities have been measured electrophysiologically,
but these data are from immature brains and do not give precise infor
mation on the concentrations of the individual transporter subtypes. H
ere we show by quantitative immunoblotting that the numbers of the ast
roglial glutamate transporters G;AST (EAAT1) and GLT (EAAT2) are 3200
and 12,000 per mu m(3) tissue in the stratum radiatum of adult rat hip
pocampus (CA1) and 18,000 and 2800 in the cerebellar molecular layer,
respectively. The total astroglial cell surface is 1.4 and 3.8 m(2)/cm
(3) in the two regions, respectively, implying average densities of GL
AST and GLT molecules in the membranes around 2300 and 8500 mu m(-2) i
n the former and 4700 and 740 mu m(-2) in the latter region. The total
concentration of glial glutamate transporters in both regions corresp
onds to three to five limes the estimated number of glutamate molecule
s in one synaptic vesicle from each of all glutamatergic synapses. How
ever, the role of glial glutamate transporters in limiting synaptic sp
illover is likely to vary between the two regions because of differenc
es in the distribution of astroglia. Synapses are completely ensheathe
d and separated from each other by astroglia in the cerebellar molecul
ar layer. In contrast, synapses in hippocampus (stratum radiatum) are
only contacted by astroglia and are often found side by side without i
ntervening glial processes.