scholarly journals Anion Conductance Behavior of the Glutamate Uptake Carrier in Salamander Retinal Glial Cells

1996 ◽  
Vol 16 (21) ◽  
pp. 6722-6731 ◽  
Author(s):  
Brian Billups ◽  
David Rossi ◽  
David Attwell
2001 ◽  
Vol 86 (2) ◽  
pp. 836-844 ◽  
Author(s):  
Dominic Mort ◽  
Païkan Marcaggi ◽  
James Grant ◽  
David Attwell

A rise of brain ammonia level, as occurs in liver failure, initially increases glutamate accumulation in neurons and glial cells. We investigated the effect of acute exposure to ammonia on glutamate transporter currents in whole cell clamped glial cells from the salamander retina. Ammonia potentiated the current evoked by a saturating concentration ofl-glutamate, and decreased the apparent affinity of the transporter for glutamate. The potentiation had a Michaelis-Menten dependence on ammonia concentration, with a K m of 1.4 mM and a maximum potentiation of 31%. Ammonia also potentiated the transporter current produced by d-aspartate. Potentiation of the glutamate transport current was seen even with glutamine synthetase inhibited, so ammonia does not act by speeding glutamine synthesis, contrary to a suggestion in the literature. The potentiation was unchanged in the absence of Cl− ions, showing that it is not an effect on the anion current gated by the glutamate transporter. Ammonium ions were unable to substitute for Na+in driving glutamate transport. Although they can partially substitute for K+ at the cation counter-transport site of the transporter, their occupancy of these sites would produce a potentiation of <1%. Ammonium, and the weak bases methylamine and trimethylamine, increased the intracellular pH by similar amounts, and intracellular alkalinization is known to increase glutamate uptake. Methylamine and trimethylamine potentiated the uptake current by the amount expected from the known pH dependence of uptake, but ammonia gave a potentiation that was larger than could be explained by the pH change, and some potentiation of uptake by ammonia was still seen when the internal pH was 8.8, at which pH further alkalinization does not increase uptake. These data suggest that ammonia speeds glutamate uptake both by increasing cytoplasmic pH and by a separate effect on the glutamate transporter. Approximately two-thirds of the speeding is due to the pH change.


2010 ◽  
Vol 104 (2) ◽  
pp. 713-725 ◽  
Author(s):  
Hui Nie ◽  
Haijun Zhang ◽  
Han-Rong Weng

Bidirectional interactions between neurons and glial cells are crucial to the genesis of pathological pain. The mechanisms regulating these interactions and the role of this process in relaying synaptic input in the spinal dorsal horn remain to be established. We studied the role of glutamate transporters in the regulation of such interactions. On pharmacological blockade of glutamate transporters, slow inward currents (SICs) appeared spontaneously and/or were evoked by peripheral synaptic input in the spinal superficial dorsal horn neurons, including the spinothalamic tract neurons. We showed that the SICs were induced by the release of glutamate from glial cells. On inhibition of glutamate uptake, the stimulation-induced, synaptically released glutamate activated glial cells and caused glial cells to release glutamate. Glial-derived glutamate acted on extrasynaptic N-methyl-d-aspartate (NMDA) receptors mainly composed of NR2B receptors and generated SICs, which led to depolarization and action potential generation in superficial spinal dorsal horn neurons. Thus glutamate transporters regulate glutamatergic neuron–glia interactions at spinal sensory synapses. When glutamate uptake is impaired, glial cells function like excitatory interneurons—they are activated by peripheral synaptic input and release glutamate to activate postsynaptic neurons in spinal pain pathways.


2005 ◽  
Vol 244 (3) ◽  
pp. 359-363 ◽  
Author(s):  
Tsutomu Sakai ◽  
Takashi Yoshitoshi ◽  
Yukiko Nagai ◽  
Kenji Kitahara

Nature ◽  
1988 ◽  
Vol 335 (6189) ◽  
pp. 433-435 ◽  
Author(s):  
Boris Barbour ◽  
Helen Brew ◽  
David Attwell

2015 ◽  
Vol 40 (11) ◽  
pp. 2317-2324 ◽  
Author(s):  
Alain M. Guillem ◽  
Zila Martínez-Lozada ◽  
Luisa C. Hernández-Kelly ◽  
Esther López-Bayghen ◽  
Bruno López-Bayghen ◽  
...  

Nature ◽  
1989 ◽  
Vol 342 (6252) ◽  
pp. 918-920 ◽  
Author(s):  
Boris Barbour ◽  
Marek Szatkowski ◽  
Nick Ingledew ◽  
David Attwell

Diabetologia ◽  
2005 ◽  
Vol 48 (2) ◽  
pp. 351-360 ◽  
Author(s):  
M. M. Ward ◽  
A. I. Jobling ◽  
M. Kalloniatis ◽  
E. L. Fletcher
Keyword(s):  

Patch-clamp recording from the plasmalemma of rat cultured astrocytes reveals the presence of both voltage-dependent sodium and voltage-dependent potassium conductances. These conductances are similar but not identical to the corresponding conductances in the axolemma. Whereas the h ∞ relation of the sodium channels has the same voltage dependence as in the nodal axolemma, the peak current-voltage relation is shifted by about 30 mV along the voltage axis in the depolarizing direction. It is speculated that the glial cells synthesize sodium and potassium channels for later insertion into the axolemma of neighbouring axons. The astrocytes also express a plasmalemmal voltage-dependent anion conductance that is turned on at about —40 mV (that is, near the resting potential of the cultured astrocytes). The channels involved are large enough to be just permeable to glutamate but not to ascorbate. It is suggested that the conductance of this channel for chloride plays a physiological role in the spatial buffering of pottassium by glial cells.


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