Abundance and ultrastructural diversity of neuronal gap junctions in the OFF and ON sublaminae of the inner plexiform layer of rat and mouse retina

• Published in: Neuroscience Vol. 142; no. 4; pp. 1093 - 1117
• Main Authors: Kamasawa, N., Furman, C.S., Davidson, K.G.V., Sampson, J.A., Magnie, A.R., Gebhardt, B.R., Kamasawa, M., Yasumura, T., Zumbrunnen, J.R., Pickard, G.E., Nagy, J.I., Rash, J.E.
• Format: Journal Article
• Language: English
• Published: Oxford Elsevier Ltd 03.11.2006; Elsevier
• Subjects: Animals; Biological and medical sciences; Cell Communication - physiology; Cell Membrane - physiology; Cell Membrane - ultrastructure; confocal immunocytochemistry; connexin36; Cx36; Eye and associated structures. Visual pathways and centers. Vision; Female; Freeze Fracturing; freeze-fracture replica immunogold labeling; FRIL; Fundamental and applied biological sciences. Psychology; Gap Junctions - physiology; Gap Junctions - ultrastructure; Male; Mice; Mice, Inbred C57BL; Microscopy, Confocal; Microscopy, Immunoelectron; Models, Neurological; Neural Pathways - physiology; Neural Pathways - ultrastructure; Neurons - physiology; Neurons - ultrastructure; Photic Stimulation; Rats; Rats, Sprague-Dawley; Retina - physiology; Retina - ultrastructure; Retinal Rod Photoreceptor Cells - physiology; Retinal Rod Photoreceptor Cells - ultrastructure; Vertebrates: nervous system and sense organs; Vision, Ocular - physiology; connexin36; LM; IPL; SPB; INL; IgG; OPL; ONL; E-face; FRIL; Cx57; P-face; Cx36; confocal immunocytochemistry; PSD; SDS; D C; IMP; GCL; ZO-1; Cx45; freeze-fracture replica immunogold labeling; LE; TBSTr; TEM; Rat; Immunocytochemistry; Rodentia; Cell junction; Retina; Gap junction; Eye; Visual system; Vertebrata; Mammalia; Mouse; Ultrastructure; Animal; Inner plexiform layer
• ISSN: 0306-4522; 1873-7544
• DOI: 10.1016/j.neuroscience.2006.08.020

Neuronal gap junctions are abundant in both outer and inner plexiform layers of the mammalian retina. In the inner plexiform layer (IPL), ultrastructurally-identified gap junctions were reported primarily in the functionally-defined and anatomically-distinct ON sublamina, with few reported in the OFF sublamina. We used freeze-fracture replica immunogold labeling and confocal microscopy to quantitatively analyze the morphologies and distributions of neuronal gap junctions in the IPL of adult rat and mouse retina. Under “baseline” conditions (photopic illumination/general anesthesia), 649 neuronal gap junctions immunogold-labeled for connexin36 were identified in rat IPL, of which 375 were photomapped to OFF vs. ON sublaminae. In contrast to previous reports, the volume-density of gap junctions was equally abundant in both sublaminae. Five distinctive morphologies of gap junctions were identified: conventional crystalline and non-crystalline “plaques” (71% and 3%), plus unusual “string” (14%), “ribbon” (7%) and “reticular” (2%) forms. Plaque and reticular gap junctions were distributed throughout the IPL. However, string and ribbon gap junctions were restricted to the OFF sublamina, where they represented 48% of gap junctions in that layer. In string and ribbon junctions, curvilinear strands of connexons were dispersed over 5 to 20 times the area of conventional plaques having equal numbers of connexons. To define morphologies of gap junctions under different light-adaptation conditions, we examined an additional 1150 gap junctions from rats and mice prepared after 30 min of photopic, mesopic and scotopic illumination, with and without general anesthesia. Under these conditions, string and ribbon gap junctions remained abundant in the OFF sublamina and absent in the ON sublamina. Abundant gap junctions in the OFF sublamina of these two rodents with rod-dominant retinas revealed previously-undescribed but extensive pathways for inter-neuronal communication; and the wide dispersion of connexons in string and ribbon gap junctions suggests unique structural features of gap junctional coupling in the OFF vs. ON sublamina.