• B Völgyi, G Debertin, M Balogh, E Popovich, and T Kovács-Öller.
• Department of Experimental Zoology and Neurobiology, University of Pécs, Pécs H-7624, Hungary; János Szentágothai Research Center, Pécs H-7624, Hungary; Department of Ophthalmology, New York University Langone Medical Center, New York, NY 10016, USA. Electronic address: volgyi01@gamma.ttk.pte.hu.
• Neuroscience. 2014 Jun 13;270:88-97.

AbstractTyrosine-hydroxylase-positive (TH(+)) amacrine cells release dopamine in a paracrine manner and also form GABA-ergic contact sites with inner retinal neurons. The best known sites are formed by TH(+) fibrous rings and AII amacrine cell somata in stratum 1 of the inner plexiform layer (IPL). An AII amacrine cell is a highly compartmentalized neuron with relatively large soma, a stout dendritic stalk and two sets of processes, one showing lobular appearance and extending horizontally in stratum 1 and a second transversally elongated group of fibers in strata 4 and 5. Although, all of these compartments have been reported as tic sites, it is uncertain if TH(+) amacrine cell inputs are homogeneously distributed or they rather target specific AII cell compartments. In this study we investigated the TH(+)/AII cell system by immunohistochemistry to map the potential synaptic contacts in the rabbit retina. We found numerous intimate contacts between the two amacrine cell populations throughout the IPL. However, TH(+) fibers favored the soma/main stalk region of AII amacrine cells and only contacted lobular appendages and transversal processes sporadically. In addition to the well-studied contacts between AII cell somata and TH(+) rings in stratum 1 we found that the main stalk region in stratum 3 serves as a secondary major target for TH(+) axons. These data thus clearly show that TH(+) contacts to AII amacrine cells are highly compartment specific.Copyright © 2014 IBRO. Published by Elsevier Ltd. All rights reserved.

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