2011
DOI: 10.1016/j.conb.2011.01.008
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Illuminating synapses and circuitry in the retina

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Cited by 15 publications
(14 citation statements)
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“…So, one possible mechanism for the OFF-time-dependent ON response changes is that prolonged light OFF interval can increase glutamate released by cones (Yang, 2004; Oesch et al, 2011), which results in a decrement in the intracellular calcium concentration in ON bipolar cells and increases these cells' activity to the following light ON stimulation, and eventually elevates the ON responsiveness of RGCs.…”
Section: Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…So, one possible mechanism for the OFF-time-dependent ON response changes is that prolonged light OFF interval can increase glutamate released by cones (Yang, 2004; Oesch et al, 2011), which results in a decrement in the intracellular calcium concentration in ON bipolar cells and increases these cells' activity to the following light ON stimulation, and eventually elevates the ON responsiveness of RGCs.…”
Section: Discussionmentioning
confidence: 99%
“…It was reported that ON cone bipolar cells can cross-inhibit OFF bipolar cells and OFF RGCs through the activation of AII amacrine cells (Margolis and Detwiler, 2007; Oesch et al, 2011), and thus extend the dynamic range of signaling in the OFF pathway (Manookin et al, 2008). Furthermore, ON and OFF RGCs have different excitatory and inhibitory synaptic inputs, which results in different spike time and spike count variability in these cells (Uzzell and Chichilnisky, 2004; Murphy and Rieke, 2006).…”
Section: Discussionmentioning
confidence: 99%
“…Synaptic transmission occurs at two levels of connectivity: photoreceptor → bipolar cell in the outer retina and bipolar cell → RGC in the inner retina (Figure 2). Excitatory signaling at both levels is modulated by two major classes of interneurons: horizontal cells in the outer retina, which are GABAergic, and amacrine cells in the inner retina, which are mostly (but not entirely) GABAergic and glycinergic (Oesch et al, 2011; Wassle and Boycott, 1991). Three major classes of glia (astrocytes, microglia and Müller cells) in the retina contribute to the homeostatic environment of the RGC and its response to disease-relevant stressors through a variety of signaling cascades (Johnson and Morrison, 2009; Tezel, 2008).…”
Section: Primary Rgc Vulnerability In Glaucomamentioning
confidence: 99%
“…In concordance, rods first appear as an intermediate form in agnathan species (i.e., jawless vertebrates) such as lampreys and become more evident in gnathostomes (i.e., jawed vertebrates) (Lamb, 2013) (Figure 1A). Despite functional specialization, rod morphology and phototransduction machinery are similar to those of cones (Fain et al, 2010; Morshedian and Fain, 2015), and rod signals piggyback on cone pathways in retinal circuitry (Oesch et al, 2011; Strettoi et al, 1992). On the basis of phylogenetic and anatomical analyses, rod photoreceptors were proposed to have originated from ancestral cone-like photoreceptors (Collin et al, 2009; Lamb et al, 2007).…”
Section: Introductionmentioning
confidence: 99%