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The development of intrinsic excitability in mouse retinal ganglion cells
Author(s) -
Qu Juan,
Myhr Karen L.
Publication year - 2008
Publication title -
developmental neurobiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.716
H-Index - 129
eISSN - 1932-846X
pISSN - 1932-8451
DOI - 10.1002/dneu.20653
Subject(s) - biology , neuroscience , retinal waves , retinal , intrinsically photosensitive retinal ganglion cells , giant retinal ganglion cells , retinal ganglion cell , retina , biochemistry
Activity‐dependent refinement of synaptic connections occurs throughout the developing nervous system, including the visual system. Retinal ganglion cells (RGCs) overproduce synapses then refine them in an activity‐dependent manner that segregates RGC connections into multicellular patterns, such as eye‐specific regions and retinotopic maps. Ferrets additionally segregate ON and OFF retinogeniculate pathways in an activity‐dependent manner. It was unknown whether differences in ON versus OFF intrinsic and spontaneous activity occur in postnatal mouse. The work reported here measured the intrinsic properties and spontaneous activity of morphologically identified postnatal mouse RGCs, and tested the hypothesis that mouse ON and OFF RGCs develop differences in spontaneous activity. We found developmental changes in resting potential, action potential threshold, depolarization to threshold, action potential width, action potential patterns, and maximal firing rates. These results are consistent with the maturation of the intrinsic properties of RGCs extending through the first three postnatal weeks. However, there were no differences among mouse ON, OFF, and multistratified RGCs in intrinsic excitability, spontaneous synaptic drive or spontaneous action potential patterns. The absence of differences between ON and OFF activity patterns is unlike the differences that arise in ferrets. In contrast to the ferret, the ON and OFF target neurons in the mouse are organized in a random pattern, not layers. This supports the hypothesis that the absence of systematic differences in activity results in the nonlayered distribution of retinogeniculate connections. © 2008 Wiley Periodicals, Inc. Develop Neurobiol, 2008

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