Eulenburg V, Knop G, Sedmak T, Schuster S, Hauf K, Schneider J, Feigenspan A, Joachimsthaler A, Brandstätter JH (2018)
Publication Type: Journal article
Publication year: 2018
Book Volume: 223
Pages Range: 3251-3266
Journal Issue: 7
DOI: 10.1007/s00429-018-1684-3
The amino acid glycine acts as a neurotransmitter at both inhibitory glycinergic and excitatory glutamatergic synapses predominantly in caudal regions of the central nervous system but also in frontal brain regions and the retina. After its presynaptic release and binding to postsynaptic receptors at caudal glycinergic synapses, two high-affinity glycine transporters GlyT1 and GlyT2 remove glycine from the extracellular space. Glycinergic neurons express GlyT2, which is essential for the presynaptic replenishment of the transmitter, while glial-expressed GlyT1 was shown to control the extracellular glycine concentration. Here we show that GlyT1 expressed by glycinergic amacrine cells of the retina does not only contribute to the control of the extracellular glycine concentration in the retina but is also essential for the maintenance of the glycinergic transmitter phenotype of this cell population. Specifically, loss of GlyT1 from the glycinergic AII amacrine cells impairs AII-mediated glycinergic neurotransmission and alters regulation of the extracellular glycine concentration, without changes in the overall distribution and/or size of glycinergic synapses. Taken together, our results suggest that GlyT1 expressed by amacrine cells in the retina combines functions covered by neuronal GlyT2 and glial GlyT1 at caudal glycinergic synapses.
APA:
Eulenburg, V., Knop, G., Sedmak, T., Schuster, S., Hauf, K., Schneider, J.,... Brandstätter, J.H. (2018). GlyT1 determines the glycinergic phenotype of amacrine cells in the mouse retina. Brain Structure & Function, 223(7), 3251-3266. https://dx.doi.org/10.1007/s00429-018-1684-3
MLA:
Eulenburg, Volker, et al. "GlyT1 determines the glycinergic phenotype of amacrine cells in the mouse retina." Brain Structure & Function 223.7 (2018): 3251-3266.
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