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Multiple γ‐aminobutyric acid plasma membrane transporters GAT‐1, GAT‐2, GAT‐3 in the rat retina
Author(s) -
Johnson Juliette,
Chen Ty K.,
Rickman Dennis W.,
Evans Chris,
Brecha Nicholas C.
Publication year - 1996
Publication title -
journal of comparative neurology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.855
H-Index - 209
eISSN - 1096-9861
pISSN - 0021-9967
DOI - 10.1002/(sici)1096-9861(19961111)375:2<212::aid-cne3>3.0.co;2-5
Subject(s) - inner plexiform layer , inner nuclear layer , outer nuclear layer , outer plexiform layer , ganglion cell layer , inner limiting membrane , retina , biology , amacrine cell , microbiology and biotechnology , immunostaining , biophysics , neuroscience , immunohistochemistry , immunology
γ‐Aminobutyric acid (GABA) plasma membrane transporters (GATs) influence synaptic neurotransmission by high‐affinity uptake and release of GABA. The distribution and cellular localization of GAT‐1, GAT‐2, and GAT‐3 in the rat retina have been evaluated by using affinity‐purified polyclonal antibodies directed to the C terminus of each of these GAT subtypes. Small GAT‐1‐immunoreactive cell bodies were located in the proximal inner nuclear layer (INL) and ganglion cell layer (GCL), and processes were distributed to all laminae of the interplexiform layer (IPL). Varicose processes were in the optic fiber layer (OFL) and the outer plexiform layer (OPL). Weak GAT‐1 immunostaining surrounded cells in the INL and GCL, and it was found in the OFL and OPL and in numerous processes in the outer nuclear layer (ONL) that ended at the outer limiting membrane. GAT‐1 is therefore strongly expressed by amacrine, displaced amacrine, and interplexiform cells and weakly expressed by Müller cells. GAT‐2 immunostaining was observed in the retina pigment epithelium and the nonpigmented ciliary epithelium. GAT‐3 immunoreactivity was distributed to the OFL, to all laminae of the IPL, GCL and INL, and to processes in the ONL that ended at the outer limiting membrane. Small GAT‐3‐immunoreactive cell bodies were in the proximal INL and GCL. GAT‐3 is therefore strongly expressed by Müller cells, and by some amacrine and displaced amacrine cells. Together, these observations demonstrate a heterologous distribution of GATs in the retina. These transporters are likely to take up GABA from, and perhaps release GABA into, the synaptic cleft and extracellular space. This suggests that GATs regulate GABA levels in these areas and thus influence synaptic neurotransmission. © 1996 Wiley‐Liss, Inc.