| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| Riley Ferguson, Kiyoharu J Miyagishima, Francisco M Nadal-Nicolas, Wei L. Characterizing the rod pathway in cone-dominated thirteen-lined ground squirrels. Frontiers in ophthalmology. vol 3. 2024-07-08. PMID:38974057. |
therefore, the aii's original function is likely that of a 'rod' amacrine cell, and its role in cone pathways in the mouse retina might be an adaptive feature stemming from its rod dominance. |
2024-07-08 |
2024-07-11 |
mouse |
| Chengjie He, Jingyi Peng, Jiayi Jin, Wanwen Shao, Yongxin Zheng, Liuxueying Zhon. Comparison of retinal parameters between rhesus and cynomolgus macaques. Experimental animals. vol 73. issue 1. 2024-02-14. PMID:37460311. |
dark-adapted 3.0 oscillatory potentials (reflection of amacrine cell activity) and light-adapted 30-hz flicker erg (a sensitive cone-pathway-driven response) waveforms of the ff-erg were similar in both species, while the times to peaks in dark-adapted 0.01 erg (the rod-driven response of bipolar cells) and dark-adapted 3.0 erg (combined rod and cone system responses) as well as the implicit times of the a- and b-waves in light-adapted 3.0 erg (the single-flash cone response) were substantially different. |
2024-02-14 |
2024-02-17 |
monkey |
| Clare R Gamlin, Chi Zhang, Michael A Dyer, Rachel O L Won. Distinct Developmental Mechanisms Act Independently to Shape Biased Synaptic Divergence from an Inhibitory Neuron. Current biology : CB. vol 30. issue 7. 2021-06-09. PMID:32109390. |
to gain insight, we took advantage of a compact circuit in the vertebrate retina, whereby the aii amacrine cell (aii ac) provides inhibition onto cone bipolar cell (bc) axons and retinal ganglion cell (rgc) dendrites, but makes the majority of its synapses with the bcs. |
2021-06-09 |
2023-08-13 |
mouse |
| Shubhash C Yadav, Stephan Tetenborg, Karin Dede. Gap Junctions in A8 Amacrine Cells Are Made of Connexin36 but Are Differently Regulated Than Gap Junctions in AII Amacrine Cells. Frontiers in molecular neuroscience. vol 12. 2020-09-30. PMID:31065239. |
the small-field a8 amacrine cell was shown to receive non-selective glutamatergic input from off and on cone bipolar cells at its bistratified dendrites in sublamina 1 and 4 of the inner plexiform layer. |
2020-09-30 |
2023-08-13 |
mouse |
| Cole W Graydon, Evan E Lieberman, Nao Rho, Kevin L Briggman, Joshua H Singer, Jeffrey S Diamon. Synaptic Transfer between Rod and Cone Pathways Mediated by AII Amacrine Cells in the Mouse Retina. Current biology : CB. vol 28. issue 17. 2019-10-17. PMID:30122532. |
here, we dissect a microcircuit in the mouse retina in which scotopic visual information (i.e., single photon events, luminance, contrast) is encoded by rod bipolar cells (rbcs) and distributed to parallel on and off cone bipolar cell (cbc) circuits via the aii amacrine cell, an inhibitory interneuron. |
2019-10-17 |
2023-08-13 |
mouse |
| Sammy C S Lee, Arndt Meyer, Timm Schubert, Laura Hüser, Karin Dedek, Silke Haverkam. Morphology and connectivity of the small bistratified A8 amacrine cell in the mouse retina. The Journal of comparative neurology. vol 523. issue 10. 2016-03-15. PMID:25630271. |
the results show that the bistratified a8 cell makes very similar synaptic contacts with cone bipolar cells as the rod pathway-specific aii amacrine cell. |
2016-03-15 |
2023-08-13 |
mouse |
| Robert E Marc, Bryan W Jones, Carl B Watt, James R Anderson, Crystal Sigulinsky, Scott Lauritze. Retinal connectomics: towards complete, accurate networks. Progress in retinal and eye research. vol 37. 2014-05-05. PMID:24016532. |
in particular, connectomics has permitted an aggressive refactoring of the retinal inner plexiform layer, demonstrating that network function cannot be simply inferred from stratification; exposing the complex geometric rules for inserting different cells into a shared network; revealing unexpected bidirectional signaling pathways between mammalian rod and cone systems; documenting selective feedforward systems, novel candidate signaling architectures, new coupling motifs, and the highly complex architecture of the mammalian aii amacrine cell. |
2014-05-05 |
2023-08-12 |
Not clear |
| Mean-Hwan Kim, Evan Vickers, Henrique von Gersdorf. Patch-clamp capacitance measurements and Ca²⁺ imaging at single nerve terminals in retinal slices. Journal of visualized experiments : JoVE. issue 59. 2012-05-25. PMID:22297269. |
on-type mixed bipolar cell (mb) terminals in the goldfish retina, which depolarize to light stimuli and receive mixed rod and cone photoreceptor input, are suitable for the study of ribbon-type synapses both due to their large size (~10-12 μm diameter) and to their numerous lateral and reciprocal synaptic connections with amacrine cell dendrites. |
2012-05-25 |
2023-08-12 |
Not clear |
| Deborah Langrill Beaudoin, Michael B Manookin, Jonathan B Dem. Distinct expressions of contrast gain control in parallel synaptic pathways converging on a retinal ganglion cell. The Journal of physiology. vol 586. issue 22. 2009-02-04. PMID:18832424. |
inhibitory input was measured by clamping voltage near 0 mv or by recording in the presence of ionotropic glutamate receptor (iglur) antagonists to isolate the following circuit: cone --> on cone bipolar cell --> aii amacrine cell --> off ganglion cell. |
2009-02-04 |
2023-08-12 |
Not clear |
| Hyo-Suk Park, Sung-Jin Park, Sun-Hwa Park, Myung-Hoon Chun, Su-Ja O. Shifting of parvalbumin expression in the rat retina in experimentally induced diabetes. Acta neuropathologica. vol 115. issue 2. 2008-05-21. PMID:17989985. |
the aii amacrine cell, a unique rod signal integrator passing through the cone bipolar cell to ganglion cells, uses parvalbumin as a transducer of cytosolic calcium ion signals in the mammalian retina. |
2008-05-21 |
2023-08-12 |
rat |
| Hyo-Suk Park, Sung-Jin Park, Sun-Hwa Park, Myung-Hoon Chun, Su-Ja O. Shifting of parvalbumin expression in the rat retina in experimentally induced diabetes. Acta neuropathologica. vol 115. issue 2. 2008-05-21. PMID:17989985. |
in addition to these parvalbumin immunoreactive amacrine cell types, a type of cone bipolar cells co-expressing glutamate transporter 1b and connecting electrically with aii amacrine cells appeared clearly by 4 weeks of diabetes, and thereafter sharply increased in number to that of aii amacrine cells. |
2008-05-21 |
2023-08-12 |
rat |
| Daniel Sun, Algis J Vingrys, Michael Kalloniati. Metabolic and functional profiling of the ischemic/reperfused rat retina. The Journal of comparative neurology. vol 505. issue 1. 2008-01-09. PMID:17729266. |
in addition to the known selective losses of amacrine cell types within the inner nuclear layer, we now demonstrate a selective loss of theme classes representing cone bipolar cells within the bipolar cell population. |
2008-01-09 |
2023-08-12 |
rat |
| Ji-Jie Pang, Muhammad M Abd-El-Barr, Fan Gao, Debra E Bramblett, David L Paul, Samuel M W. Relative contributions of rod and cone bipolar cell inputs to AII amacrine cell light responses in the mouse retina. The Journal of physiology. vol 580. issue Pt. 2. 2007-07-19. PMID:17255172. |
relative contributions of rod and cone bipolar cell inputs to aii amacrine cell light responses in the mouse retina. |
2007-07-19 |
2023-08-12 |
mouse |
| Theresa Puthussery, Erica L Fletche. P2X2 receptors on ganglion and amacrine cells in cone pathways of the rat retina. The Journal of comparative neurology. vol 496. issue 5. 2006-06-08. PMID:16615123. |
immunoelectron microscopy revealed that p2x(2)-immunoreactive amacrine cell processes were associated with cone bipolar cell axon terminals as well as other conventional synapses in the inner plexiform layer. |
2006-06-08 |
2023-08-12 |
rat |
| Theresa Puthussery, Erica L Fletche. P2X2 receptors on ganglion and amacrine cells in cone pathways of the rat retina. The Journal of comparative neurology. vol 496. issue 5. 2006-06-08. PMID:16615123. |
it was interesting that p2x(2)r-immunoreactive amacrine cell dendrites stratified in the sublaminae of the inner plexiform layer occupied by cone, but not rod bipolar cell axon terminals. |
2006-06-08 |
2023-08-12 |
rat |
| Tae-Hoon Kang, Yeon-Kyung Choi, In-Beom Kim, Su-Ja Oh, Myung-Hoon Chu. Identification and characterization of an aquaporin 1 immunoreactive amacrine-type cell of the mouse retina. The Journal of comparative neurology. vol 488. issue 3. 2005-10-31. PMID:15952169. |
in summary, a gabaergic amacrine cell type labeled by an antibody against aqp1 was identified in the mouse retina and was found to play a possible role in transferring a certain type of visual information from other amacrine or a few cone bipolar cells primarily to ganglion cells. |
2005-10-31 |
2023-08-12 |
mouse |
| Kareem M Ahmad, Karl Klug, Steve Herr, Peter Sterling, Stan Schei. Cell density ratios in a foveal patch in macaque retina. Visual neuroscience. vol 20. issue 2. 2003-11-28. PMID:12916740. |
we also find one (1.01) müller cell, one (1.01) amacrine cell in the inner nuclear layer, and close to one (0.83) horizontal cell for each cone pedicle. |
2003-11-28 |
2023-08-12 |
monkey |
| Ramon F Dacheux, Melissa F Chimento, Franklin R Amtho. Synaptic input to the on-off directionally selective ganglion cell in the rabbit retina. The Journal of comparative neurology. vol 456. issue 3. 2003-03-21. PMID:12528191. |
this microcircuit consisted of two cone bipolar cell terminal dyad synapses where one dyad contained an amacrine cell process making a reciprocal synapse and a ds ganglion cell dendrite receiving direct excitation; the other dyad synapse, found lateral to the first dyad, contained two amacrine cell processes that both made reciprocal synapses, but one fed forward to make a putative inhibitory synapse with the ds cell dendrite. |
2003-03-21 |
2023-08-12 |
rabbit |
| In-Beom Kim, Eun-Jin Lee, Su-Ja Oh, Cheol-Beom Park, David V Pow, Myung-Hoon Chu. Light and electron microscopic analysis of aquaporin 1-like-immunoreactive amacrine cells in the rat retina. The Journal of comparative neurology. vol 452. issue 2. 2002-10-30. PMID:12271491. |
their most frequent synaptic input was from other amacrine cell processes in both sublaminae a and b of the ipl, followed by a few cone bipolar cells. |
2002-10-30 |
2023-08-12 |
rat |
| S H DeVries, D A Baylo. An alternative pathway for signal flow from rod photoreceptors to ganglion cells in mammalian retina. Proceedings of the National Academy of Sciences of the United States of America. vol 92. issue 23. 1995-12-21. PMID:7479860. |
rod signals in the mammalian retina are thought to reach ganglion cells over the circuit rod-->rod depolarizing bipolar cell-->aii amacrine cell-->cone bipolar cells-->ganglion cells. |
1995-12-21 |
2023-08-12 |
rabbit |