Loss of Stim2 in zebrafish induces glaucoma-like phenotype

Authors: Sofiia Baranykova, Rishikesh Kumar Gupta, Arkadiusz Kajdasz, Iga Wasilewska, Matylda Macias, Aleksandra Szybinska, Tomasz Węgierski, Karim Abu Nahia, Shamba S. Mondal, Cecilia L. Winata, Jacek Kuźnicki, Lukasz Majewski

Source: Scientific Reports, Vol 14, Iss 1, Pp 1-18 (2024)

Subject Terms: Stim2, SOCE, Retina, scRNA-seq, GABAergic amacrine cells, Glaucoma, Medicine, Science

File Description: electronic resource

Relation: https://doaj.org/toc/2045-2322

Access URL: https://doaj.org/article/ef3c06b4afc24f27a586cb85f8a34536

Retinal Cell Biology in Health and Disease

Contributors: Ameri, Hossein

Subject Terms: retina, multiphoton fluorescence lifetime imaging microscopy, FLIM, NAD(P)H, metabolic imaging, glycolysis, oxidative phosphorylation, Alzheimer’s disease, retinal vascular physiology biomarkers, 5XFAD, amyloid β, active targeting, choroidal neovascularization, exosome, choriocapillaris, mast cells, macrophages, smooth muscle cells, uveal diseases, age-related macular degeneration, ganglion cells, amacrine cells, optic nerve crush, depth perception, recessive Stargardt disease (STGD1), retinal pigment epithelium (RPE), complement system, bisretinoid-lipofuscin, 'disease-in-a-dish', retinoids, macular degeneration, ABCA4, subretinal injection, gene therapy, U1 snRNA, U6 snRNA, AAV, splice correction, Opa1, ADOA, optic atrophy, therapeutic treatment, transition metals, laser ablation inductively coupled plasma-mass spectrometry, diabetic retinopathy, diabetes mellitus, microvascular complication, neuronal dysfunction, neurodegeneration, clinic therapy, RCBTB1, inherited retinal disease, retinal pigment epithelium, oxidative stress, mitochondria, cone cell, photoreceptor, synapse, retinal detachment, Rho kinase, synaptic ribbons, pedicle, spherule, STED microscopy, pig, marmoset, primary cells, angiogenesis, potassium channel, endothelial cell, peptide Lv, protein trafficking, signaling pathway, ribbon synapse, rabconnectin-3α, DMXL2, vesicular H+-ATPase, Rab3, retinitis pigmentosa, retinal pigmented epithelium, retinal degeneration, secretome, Royal College of Surgeons rat, leber hereditary optic neuropathy, LHON, NADH dehydrogenase, retinal ganglion cells, mitochondrial inheritance, idebenone, blood–retinal barrier, disheveled, claudin-5, tight junction, norrin, endothelium, permeability, barriergenesis, Wnt signaling, mitophagy, lysosome, BCKDK, βA3/A1-crystallin, astrocytes, autophagy, optic nerve, multiple sclerosis (MS), optic neuritis, laser speckle flowgraphy (LSFG), optical coherence tomography angiography (OCTA), retinal vasculature, retinal blood flow, retinal vascular inflammation, biomarker, Medicine: general issues

File Description: application/octet-stream

Access URL: https://directory.doabooks.org/handle/20.500.12854/137862
https://mdpi.com/books/pdfview/book/9102

Retinal pharmacodynamic and pharmacokinetic profile of cannabidiol in an in vivo model of retinal excitotoxicity

Authors: Conti, Federica ^{a, 1}, Lazzara, Francesca ^{a, 1}, Thermos, Kyriaki ^{b, ⁎⁎}, Zingale, Elide ^{c, d}, Spyridakos, Dimitris ^b, Romano, Giovanni Luca ^e, Di Martino, Serena ^a, Micale, Vincenzo ^a, Kuchar, Martin ^{f, g}, Spadaro, Angelo ^h, Pignatello, Rosario ^{c, d}, Rossi, Settimio ⁱ, D'Amico, Michele ^j, Maria Platania, Chiara Bianca ^{a, k}, Drago, Filippo ^{a, k}, Bucolo, Claudio ^{a, k, ⁎}

Source: In European Journal of Pharmacology 15 March 2025 991

GABAergic amacrine cells balance biased chromatic information in the mouse retina

Authors: Korympidou, Maria M. ^{1, 2, 3, 8}, Strauss, Sarah ^{2, 3, 4, 8}, Schubert, Timm ^{1, 2}, Franke, Katrin ⁶, Berens, Philipp ^{2, 4, 5}, Euler, Thomas ^{1, 2, 9, ∗}, Vlasits, Anna L. ^{1, 2, 7, ∗∗}

Source: In Cell Reports 26 November 2024 43(11)

Pten regulates endocytic trafficking of cell adhesion and Wnt signaling molecules to pattern the retina

Authors: Touahri, Yacine ^{1, 2, 3}, Hanna, Joseph ^{1, 3, 4}, Tachibana, Nobuhiko ^{1, 5}, Okawa, Satoshi ^{6, 7, 8, 9}, Liu, Hedy ^{1, 2}, David, Luke Ajay ^{1, 3, 4}, Olender, Thomas ¹⁰, Vasan, Lakshmy ^{1, 4}, Pak, Alissa ^{1, 4}, Mehta, Dhruv Nimesh ^{1, 2, 3}, Chinchalongporn, Vorapin ^{1, 2}, Balakrishnan, Anjali ^{1, 2, 5}, Cantrup, Robert ⁵, Dixit, Rajiv ^{1, 2}, Mattar, Pierre ¹¹, Saleh, Fermisk ^{1, 2}, Ilnytskyy, Yaroslav ¹², Murshed, Monzur ¹³, Mains, Paul E. ⁵, Kovalchuk, Igor ¹², Lefebvre, Julie L. ^{14, 15}, Leong, Hon S. ^{1, 16}, Cayouette, Michel ¹¹, Wang, Chao ^{1, 17}, del Sol, Antonio ^{6, 18, 19}, Brand, Marjorie ¹⁰, Reese, Benjamin E. ²⁰, Schuurmans, Carol ^{1, 2, 3, 4, 5, 21, ∗}

Source: In Cell Reports 23 April 2024 43(4)

Starburst amacrine cells, involved in visual motion perception, lose their synaptic input from dopaminergic amacrine cells and degenerate in Parkinson’s disease patients

Authors: Xavier Sánchez-Sáez, Isabel Ortuño-Lizarán, Carla Sánchez-Castillo, Pedro Lax, Nicolás Cuenca

Source: Translational Neurodegeneration, Vol 12, Iss 1, Pp 1-16 (2023)

Subject Terms: Parkinson’s disease, Retinal neurodegeneration, Human retina, ChAT amacrine cells, Dopaminergic amacrine cells, Neurology. Diseases of the nervous system, RC346-429

File Description: electronic resource

Relation: https://doaj.org/toc/2047-9158

Access URL: https://doaj.org/article/00736fbb7bb444c692ce47c80c3b6da4

Starburst amacrine cells amplify optogenetic visual restoration through gap junctions

Authors: Yusaku Katada, Hiromitsu Kunimi, Naho Serizawa, Deokho Lee, Kenta Kobayashi, Kazuno Negishi, Hideyuki Okano, Kenji F. Tanaka, Kazuo Tsubota, Toshihide Kurihara

Source: Molecular Therapy: Methods & Clinical Development, Vol 30, Iss , Pp 1-13 (2023)

Subject Terms: retina, gene therapy, optogenetics, visual restoration, starburst amacrine cells, Genetics, QH426-470, Cytology, QH573-671

File Description: electronic resource

Relation: http://www.sciencedirect.com/science/article/pii/S2329050123000736; https://doaj.org/toc/2329-0501

Access URL: https://doaj.org/article/2eb99aaf89804103af13347c0cff9850

Activation of oxytocin receptors in mouse GABAergic amacrine cells modulates retinal dopaminergic signaling

Authors: Songhui Hu, Yurong Wang, Xu Han, Min Dai, Yongxing Zhang, Yuanyuan Ma, Shijun Weng, Lei Xiao

Source: BMC Biology, Vol 20, Iss 1, Pp 1-18 (2022)

Subject Terms: Oxytocin receptor, Visual information processing, Retinal amacrine cells, Dopamine, Electroretinographic recording, Biology (General), QH301-705.5

File Description: electronic resource

Relation: https://doaj.org/toc/1741-7007

Access URL: https://doaj.org/article/052b8f42104f4d53a7ff0029ae74064c

Levodopa Rescues Retinal Function in the Transgenic A53T Alpha-Synuclein Model of Parkinson’s Disease

Authors: Katie K. N. Tran, Vickie H. Y. Wong, Kirstan A. Vessey, David I. Finkelstein, Bang V. Bui, Christine T. O. Nguyen

Source: Biomedicines, Vol 12, Iss 1, p 130 (2024)

Subject Terms: A53T mice, levodopa, Parkinson’s disease, electroretinography, optical coherence tomography, amacrine cells, Biology (General), QH301-705.5

File Description: electronic resource

Relation: https://www.mdpi.com/2227-9059/12/1/130; https://doaj.org/toc/2227-9059

Access URL: https://doaj.org/article/bc49c8d44bd9418990fec166293f6114

Starburst amacrine cells form gap junctions in the early postnatal stage of the mouse retina

Authors: Takuma Maruyama, Toshiyuki Ishii, Makoto Kaneda

Source: Frontiers in Cellular Neuroscience, Vol 17 (2023)

Subject Terms: starburst amacrine cells (SACs), gap junction, connexin (Cx), retinal ganglion cell (RGC), dopamine D1 receptor (D1R), visual experience, Neurosciences. Biological psychiatry. Neuropsychiatry, RC321-571

File Description: electronic resource

Relation: https://www.frontiersin.org/articles/10.3389/fncel.2023.1173579/full; https://doaj.org/toc/1662-5102

Access URL: https://doaj.org/article/6c1efb03193643269cca84833ac18379

Retinal self-organization: a model of retinal ganglion cells and starburst amacrine cells mosaic formation

Authors: Jean de Montigny, Evelyne Sernagor, Roman Bauer

Source: Open Biology, Vol 13, Iss 4 (2023)

Subject Terms: self-organization, retinal mosaic, computational modelling, retinal ganglion cells, starburst amacrine cells, Biology (General), QH301-705.5

File Description: electronic resource

Relation: https://doaj.org/toc/2046-2441

Access URL: https://doaj.org/article/19a750ac3ccc40d8a5dd79fb7d6867c1

Special nuclear layer contacts between starburst amacrine cells in the mouse retina

Authors: Shang Mu, Nicholas L. Turner, William M. Silversmith, Chris S. Jordan, Nico Kemnitz, Marissa Sorek, Celia David, Devon L. Jones, Doug Bland, Merlin Moore, Amy Robinson Sterling, H. Sebastian Seung

Source: Frontiers in Ophthalmology, Vol 3 (2023)

Subject Terms: starburst amacrine cells (SACs), electron microscopy, retina, 3D reconstruction, perisomatic contact, Medicine

File Description: electronic resource

Relation: https://www.frontiersin.org/articles/10.3389/fopht.2023.1129463/full; https://doaj.org/toc/2674-0826

Access URL: https://doaj.org/article/184aa68f0b8a46729003108cc885c12d

Spatiotemporal properties of glutamate input support direction selectivity in the dendrites of retinal starburst amacrine cells

Authors: Prerna Srivastava, Geoff de Rosenroll, Akihiro Matsumoto, Tracy Michaels, Zachary Turple, Varsha Jain, Santhosh Sethuramanujam, Benjamin L Murphy-Baum, Keisuke Yonehara, Gautam Bhagwan Awatramani

Source: eLife, Vol 11 (2022)

Subject Terms: starburst amacrine cells, retinal circuitry, direction selectivity, iGluSnFR, bipolar cells, space-time wiring, Medicine, Science, Biology (General), QH301-705.5

File Description: electronic resource

Relation: https://elifesciences.org/articles/81533; https://doaj.org/toc/2050-084X

Access URL: https://doaj.org/article/ed877c5e6b144b93b97fa5ba0b5fc820

Changes in Starburst Amacrine Cells in Mice with Diabetic Retinopathy

Authors: Jae-Rim Son, Myung-Jun Lee, Chang-Jin Jeon

Source: Frontiers in Bioscience-Landmark, Vol 28, Iss 5, p 92 (2023)

Subject Terms: starburst amacrine cells, diabetic retinopathy, streptozotocin, choline acetyltransferase, calcium-binding proteins, immunocytochemistry, Biochemistry, QD415-436, Biology (General), QH301-705.5

File Description: electronic resource

Relation: https://www.imrpress.com/journal/FBL/28/5/10.31083/j.fbl2805092; https://doaj.org/toc/2768-6701

Access URL: https://doaj.org/article/ab86c94c685a4c73b0b2d24aa848ca28

Time-Lapse Imaging of Neuronal Arborization using Sparse Adeno-Associated Virus Labeling of Genetically Targeted Retinal Cell Populations

Authors: Samantha Ing-Esteves, author^{1, 2}, Julie L. Lefebvre, author^{1, 2}

Source: Journal of Visualized Experiments. (169)

Availability: http://www.jove.com/video/62308

Transpupillary Two-Photon In Vivo Imaging of the Mouse Retina

Authors: Zelun Wang, author^{1, 2}, Sean McCracken, author^{1, 2}, Philip R. Williams, author^{1, 3, 4}

Source: Journal of Visualized Experiments. (168)

Availability: http://www.jove.com/video/61970

Trilogy Development of Proopiomelanocortin Neurons From Embryonic to Adult Stages in the Mice Retina

Authors: Xuhong Zhang, Xiaoyu Wang, Senjie Wang, Wei Peng, Rahim Ullah, Junfen Fu, Yudong Zhou, Ye Shen

Source: Frontiers in Cell and Developmental Biology, Vol 9 (2021)

Subject Terms: POMC-positive neurons, amacrine cells, development, retina, embryonic, Biology (General), QH301-705.5

File Description: electronic resource

Relation: https://www.frontiersin.org/articles/10.3389/fcell.2021.718851/full; https://doaj.org/toc/2296-634X

Access URL: https://doaj.org/article/2f0e687f5cc047ad8a982d5f94bb224b

Glial contribution to cyclodextrin-mediated reversal of cholesterol accumulation in murine NPC1-deficient neurons in vivo

Authors: Amélie Barthelemy, Valérie Demais, Izabela-Cristina Stancu, Eugeniu Vasile, Tom Houben, Michael Reber, Valentina Pallottini, Martine Perraut, Sophie Reibel, Frank W. Pfrieger

Source: Neurobiology of Disease, Vol 158, Iss , Pp 105469- (2021)

Subject Terms: Lysosome, Intravitreal, Cyclodextrin, Inherited metabolic disease, Ganglion cells, Amacrine cells, Neurosciences. Biological psychiatry. Neuropsychiatry, RC321-571

File Description: electronic resource

Relation: http://www.sciencedirect.com/science/article/pii/S0969996121002187; https://doaj.org/toc/1095-953X

Access URL: https://doaj.org/article/403658d39f4344499eda03063ddd8fad

Is there a relationship between dopamine and rhegmatogenous retinal detachment?

Authors: Alessio Martucci, Massimo Cesareo, Maria Dolores Pinazo-Durán, Michela Di Pierro, Matteo Di Marino, Carlo Nucci, Massimiliano Coletta, Raffaele Mancino

Source: Neural Regeneration Research, Vol 15, Iss 2, Pp 311-314 (2020)

Subject Terms: 4-dihydroxyphenylacetic acid, DOPAC, dopamine, dopaminergic amacrine cells, dopaminergic neurotoxicity, macular pucker, oxidative stress, photoreceptor degeneration, rhegmatogenous retinal detachment, vitreous hemorrhage, Neurology. Diseases of the nervous system, RC346-429

File Description: electronic resource

Relation: http://www.nrronline.org/article.asp?issn=1673-5374;year=2020;volume=15;issue=2;spage=311;epage=314;aulast=Martucci; https://doaj.org/toc/1673-5374

Access URL: https://doaj.org/article/1b955617161a4bf19079a653043c1365

GABA release selectively regulates synapse development at distinct inputs on direction-selective retinal ganglion cells

Authors: Bleckert, Adam, Zhang, Chi, Turner, Maxwell H., Koren, David, Berson, David M., Park, Silvia J. H., Demb, Jonathan B., Rieke, Fred, Wei, Wei, Wong, Rachel O.

Source: Proceedings of the National Academy of Sciences of the United States of America, 2018 Dec . 115(51), E12083-E12090.

Access URL: https://www.jstor.org/stable/26574257