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Connexin36 is required for gap junctional coupling of most ganglion cell subtypes in the mouse retina
Author(s) -
Pan Feng,
Paul David L.,
Bloomfield Stewart A.,
Völgyi Béla
Publication year - 2010
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/cne.22254
Subject(s) - biology , retina , neuroscience , ganglion , gap junction , coupling (piping) , anatomy , microbiology and biotechnology , intracellular , mechanical engineering , engineering
Converging evidence indicates that electrical synaptic transmission via gap junctions plays a crucial role in signal processing in the retina. In particular, amacrine and ganglion cells express numerous gap junctions, resulting in extensive electrical networks in the proximal retina. Both connexin36 (Cx36) and connexin45 (Cx45) subunits are widely distributed in the inner plexiform layer (IPL) and therefore are likely contribute to gap junctions formed by a number of ganglion cell subtypes. In the present study, we used the gap junction‐permeant tracer Neurobiotin to compare the coupling pattern of different ganglion cell subtypes in wild‐type (WT) and Cx36 knockout (KO) mouse retinas. We found that homologous ganglion‐to‐ganglion cell coupling was lost for two subtypes after deletion of Cx36, whereas two other ganglion cell subtypes retained homologous coupling in the KO mouse. In contrast, deletion of Cx36 resulted in a partial or complete loss of ganglion‐to‐amacrine cell heterologous coupling in 9 of 10 ganglion cell populations studied. Overall, our results indicate that Cx36 is the predominant subunit of gap junctions in the proximal mouse retina, expressed by most ganglion cell subtypes, and thereby likely plays a major role in the concerted activity generated by electrical synapses. J. Comp. Neurol. 518:911–927, 2010. © 2009 Wiley‐Liss, Inc.