Müller Glia in Retinal Innate Immunity: A Perspective on Their Roles in Endophthalmitis

Innate immune recognition

Janeway, C. A., & Medzhitov, R. (2002) · Annual Review of Immunology · doi:10.1146/annurev.immunol.20.083001.084359 · Cited by 8,394 · see citing works

A human homologue of the Drosophila Toll protein signals activation of adaptive immunity

Medzhitov, R., Preston-Hurlburt, P., & Janeway, C. A. J. (1997) · Nature · doi:10.1038/41131 · Cited by 6,137 · see citing works

Staphylococcus aureus Infections

Lowy, F. D. (1998) · New England Journal of Medicine · doi:10.1056/nejm199808203390806 · Cited by 6,018 · see citing works

Astrocyte-endothelial interactions at the blood-brain barrier

Abbott, N. J., Rönnbäck, L., & Hansson, E. (2006) · Nature Reviews Neuroscience · doi:10.1038/nrn1824 · Cited by 5,595 · see citing works

Microglia: a sensor for pathological events in the CNS

Kreutzberg, G. W. (1996) · Trends in Neurosciences · doi:10.1016/0166-2236(96)10049-7 · Cited by 4,396 · see citing works

Microglia: Active sensor and versatile effector cells in the normal and pathologic brain

Hanisch, U.-K., & Kettenmann, H. (2007) · Nature Neuroscience · doi:10.1038/nn1997 · Cited by 3,676 · see citing works

The Retinal Pigment Epithelium in Visual Function

Strauss, O. (2005) · Physiological Reviews · doi:10.1152/physrev.00021.2004 · Cited by 2,828 · see citing works

Tripartite synapses: glia, the unacknowledged partner

Araque, A., Parpura, V., Sanzgiri, R. P., & Haydon, P. G. (1999) · Trends in Neurosciences · doi:10.1016/s0166-2236(98)01349-6 · Cited by 2,529 · see citing works

The many roles of chemokines and chemokine receptors in inflammation

Charo, I. F., & Ransohoff, R. M. (2006) · New England Journal of Medicine · doi:10.1056/nejmra052723 · Cited by 2,523 · see citing works

TLR signaling pathways

Takeda, K., & Akira, S. (2004) · Seminars in Immunology · doi:10.1016/j.smim.2003.10.003 · Cited by 2,461 · see citing works

Proinflammatory Cytokines

Dinarello, C. A. (2000) · CHEST Journal · doi:10.1378/chest.118.2.503 · Cited by 2,047 · see citing works

Community-Associated Methicillin-Resistant <i>Staphylococcus aureus</i> : Epidemiology and Clinical Consequences of an Emerging Epidemic

David, M. Z., & Daum, R. S. (2010) · Clinical Microbiology Reviews · doi:10.1128/cmr.00081-09 · Cited by 1,972 · see citing works

Müller cells in the healthy and diseased retina

Bringmann, A., Pannicke, T., Grosche, J., Francke, M., Wiedemann, P., Skatchkov, S. N., Osborne, N. N., & Reichenbach, A. (2006) · Progress in Retinal and Eye Research · doi:10.1016/j.preteyeres.2006.05.003 · Cited by 1,905 · see citing works

A common progenitor for neurons and glia persists in rat retina late in development

Turner, D. L., & Cepko, C. L. (1987) · Nature · doi:10.1038/328131a0 · Cited by 1,430 · see citing works

The Changing Epidemiology of Staphylococcus aureus ?

Chambers, H. F. “. (2001) · Emerging infectious diseases · doi:10.3201/eid0702.010204 · Cited by 1,419 · see citing works

Glia: listening and talking to the synapse

Haydon, P. G. (2001) · Nature reviews. Neuroscience · doi:10.1038/35058528 · Cited by 1,410 · see citing works

Toll-like receptors and innate immunity

Kumar, H., Kawai, T., & Akira, S. (2009) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2009.08.062 · Cited by 1,171 · see citing works

Pathogenesis of Methicillin‐Resistant Staphylococcus aureus Infection

Gordon, R. J., & Lowy, F. D. (2008) · Clinical Infectious Diseases · doi:10.1086/533591 · Cited by 962 · see citing works

Prophylaxis of postoperative endophthalmitis following cataract surgery: Results of the ESCRS multicenter study and identification of risk factors

ESCRS Endophthalmitis Study Group (2007) · Journal of Cataract & Refractive Surgery · doi:10.1016/j.jcrs.2007.02.032 · Cited by 907 · see citing works

Ocular immune privilege: therapeutic opportunities from an experiment of nature

Streilein, J. W. (2003) · Nature Reviews Immunology · doi:10.1038/nri1224 · Cited by 807 · see citing works

The Müller cell: a functional element of the retina

Newman, E. A., & Reichenbach, A. (1996) · Trends in Neurosciences · doi:10.1016/0166-2236(96)10040-0 · Cited by 789 · see citing works

Nitric oxide and redox mechanisms in the immune response

Wink, D. A., Hines, H. B., Cheng, R. Y. S., Switzer, C. H., Flores-Santana, W., Vitek, M. P., Ridnour, L. A., & Colton, C. A. (2011) · Journal of Leukocyte Biology · doi:10.1189/jlb.1010550 · Cited by 765 · see citing works

Cellular signaling and factors involved in Müller cell gliosis: neuroprotective and detrimental effects

Bringmann, A., Iandiev, I., Pannicke, T., Wurm, A., Hollborn, M., Wiedemann, P., Osborne, N. N., & Reichenbach, A. (2009) · Progress in Retinal and Eye Research · doi:10.1016/j.preteyeres.2009.07.001 · Cited by 761 · see citing works

Receptor for Advanced Glycation End Products (RAGE)-mediated Neurite Outgrowth and Activation of NF-κB Require the Cytoplasmic Domain of the Receptor but Different Downstream Signaling Pathways

Huttunen, H. J., Fages, C., & Rauvala, H. (1999) · Journal of Biological Chemistry · doi:10.1074/jbc.274.28.19919 · Cited by 629 · see citing works

Müller glia are a potential source of neural regeneration in the postnatal chicken retina

Fischer, A. J., & Reh, T. A. (2001) · Nature Neuroscience · doi:10.1038/85090 · Cited by 579 · see citing works

Acute Endophthalmitis Following Cataract Surgery

Taban, M. (2005) · Archives of Ophthalmology · doi:10.1001/archopht.123.5.613 · Cited by 564 · see citing works

Microglia activation in retinal degeneration

Langmann, T. (2007) · Journal of Leukocyte Biology · doi:10.1189/jlb.0207114 · Cited by 496 · see citing works

Emergence of vancomycin resistant Staphylococcus aureus(VRSA) from a tertiary care hospital from northern part of India

Tiwari, H. K., & Sen, M. R. (2006) · BMC Infectious Diseases · doi:10.1186/1471-2334-6-156 · Cited by 336 · see citing works

Requirement for p38 and p44/p42 Mitogen-Activated Protein Kinases in RAGE-Mediated Nuclear Factor-κB Transcriptional Activation and Cytokine Secretion

Yeh, C.-H., Sturgis, L., Haidacher, J., Zhang, X.-N., Sherwood, S. J., Bjercke, R. J., Juhasz, O., Crow, M. T., Tilton, R. G., & Denner, L. (2001) · Diabetes · doi:10.2337/diabetes.50.6.1495 · Cited by 326 · see citing works

Injury-induced upregulation of bFGF and CNTF mRNAS in the rat retina

Wen, R., Song, Y., Cheng, T., Matthes, M. T., Yasumura, D., LaVail, M. M., & Steinberg, R. H. (1995) · Journal of Neuroscience · doi:10.1523/jneurosci.15-11-07377.1995 · Cited by 321 · see citing works

Infectious Endophthalmitis after Penetrating Injuries with Retained Intraocular Foreign Bodies

Thompson, J. T., Parver, L. M., Enger, C. L., et al. (1993) · Ophthalmology · doi:10.1016/s0161-6420(93)31454-5 · Cited by 319 · see citing works

Relationship between astrocytes, ganglion cells and vasculature of the retina

Stone, J., & Dreher, Z. (1987) · The Journal of Comparative Neurology · doi:10.1002/cne.902550104 · Cited by 298 · see citing works

Complications of intravitreal injections

Sampat, K. M., & Garg, S. J. (2010) · Current Opinion in Ophthalmology · doi:10.1097/icu.0b013e328338679a · Cited by 290 · see citing works

The role of müller cells in the formation of the blood-retinal barrier

Tout, S., Chan‐Ling, T., Holländer, H., & Stone, J. (1993) · Neuroscience · doi:10.1016/0306-4522(93)90473-s · Cited by 268 · see citing works

Ciliary neurotrophic factor and stress stimuli activate the Jak-STAT pathway in retinal neurons and glia

Peterson, W. M., Wang, Q., Tzekova, R., & Wiegand, S. J. (2000) · The Journal of Neuroscience · doi:10.1523/jneurosci.20-11-04081.2000 · Cited by 267 · see citing works

Innate immunity in the retina: Toll-like receptor (TLR) signaling in human retinal pigment epithelial cells

Kumar, M. V., Nagineni, C. N., Chin, M. S., Hooks, J. J., & Detrick, B. (2004) · Journal of Neuroimmunology · doi:10.1016/j.jneuroim.2004.04.018 · Cited by 243 · see citing works

Prognostic factors in ocular injuries caused by intraocular or retrobulbar foreign bodies

Jonas, J. B., Knorr, H. L. J., & Budde, W. M. (2000) · Ophthalmology · doi:10.1016/s0161-6420(00)00079-8 · Cited by 229 · see citing works

Adaptive Müller Cell Responses to Microglial Activation Mediate Neuroprotection and Coordinate Inflammation in the Retina

Wang, M., Ma, W., Zhao, L., Fariss, R. N., & Wong, W. T. (2011) · Journal of Neuroinflammation · doi:10.1186/1742-2094-8-173 · Cited by 228 · see citing works

Role of receptor for advanced glycation end-product (RAGE) and the JAK/STAT-signaling pathway in AGE-induced collagen production in NRK-49F cells

Huang, J., Guh, J., Chen, H., Hung, W., Lai, Y., & Chuang, L. (2001) · Journal of Cellular Biochemistry · doi:10.1002/1097-4644(20010401)81:1 · Cited by 225 · see citing works

Modification of Glial–Neuronal Cell Interactions Prevents Photoreceptor Apoptosis during Light-Induced Retinal Degeneration

Harada, T., Harada, C., Nakayama, N., Okuyama, S., Yoshida, K., Kohsaka, S., Matsuda, H., & Wada, K. (2000) · Neuron · doi:10.1016/s0896-6273(00)81185-x · Cited by 221 · see citing works

Endophthalmitis after Penetrating Trauma

Thompson, W. S., Rubsamen, P. E., Flynn, H. W., et al. (1995) · Ophthalmology · doi:10.1016/s0161-6420(95)30807-x · Cited by 221 · see citing works

Blood-neural Barrier: Intercellular Communication at Glio-Vascular Interface

Kim, J. H., Kim, J.-H., Park, J., Lee, S., Kim, W.-J., Yu, Y.-S., & Kim, K. (2006) · BMB Reports · doi:10.5483/bmbrep.2006.39.4.339 · Cited by 218 · see citing works

Development and neurogenic potential of Müller glial cells in the vertebrate retina

Jadhav, A. P., Roesch, K., & Cepko, C. L. (2009) · Progress in Retinal and Eye Research · doi:10.1016/j.preteyeres.2009.05.002 · Cited by 211 · see citing works

Hyperglycaemia-induced pro-inflammatory responses by retinal Müller glia are regulated by the receptor for advanced glycation end-products (RAGE)

Zong, H., Ward, M. S., Madden, A. F., Yong, P. H., Limb, G. A., Curtis, T. M., & Stitt, A. W. (2010) · Diabetologia · doi:10.1007/s00125-010-1900-z · Cited by 201 · see citing works

Microglia in the healthy and degenerating retina: Insights from novel mouse models

Karlstetter, M., Ebert, S., & Langmann, T. (2010) · Immunobiology · doi:10.1016/j.imbio.2010.05.010 · Cited by 197 · see citing works

Toll‐like receptor 3 agonist poly(I:C)‐induced antiviral response in human corneal epithelial cells

Kumar, A., Zhang, J., & Yu, F. X. (2005) · Immunology · doi:10.1111/j.1365-2567.2005.02258.x · Cited by 193 · see citing works

Bacterial endophthalmitis: Therapeutic challenges and host–pathogen interactions

Callegan, M. C., Gilmore, M. S., GREGORY, M., Ramadan, R. T., Wiskur, B. J., MOYER, A., HUNT, J., & Novosad, B. D. (2007) · Progress in Retinal and Eye Research · doi:10.1016/j.preteyeres.2006.12.001 · Cited by 179 · see citing works

Pathogenesis of Gram-Positive Bacterial Endophthalmitis

Callegan, M. C., Booth, M. C., Jett, B. D., et al. (1999) · Infection and Immunity · doi:10.1128/iai.67.7.3348-3356.1999 · Cited by 174 · see citing works

Retinal Glial (Müller) Cells: Sensing and Responding to Tissue Stretch

Lindqvist, N., Liu, Q., Zajadacz, J., Franze, K., & Reichenbach, A. (2010) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.09-4159 · Cited by 164 · see citing works

What do retinal Müller (glial) cells do for their neuronal ‘small siblings’?

Reichenbach, A., Stolzenburg, J. ‐., Eberhardt, W., Chao, T. I., Dettmer, D., & Hertz, L. (1993) · Journal of Chemical Neuroanatomy · doi:10.1016/0891-0618(93)90042-3 · Cited by 161 · see citing works

Neurotrophins in Cell Survival/Death Decisions

Casaccia‐Bonnefil, P., Gu, C., & Chao, M. V. (1999) · Advances in experimental medicine and biology · doi:10.1007/978-1-4615-4685-6_22 · Cited by 145 · see citing works

Eubacterial PCR for Bacterial Detection and Identification in 100 Acute Postcataract Surgery Endophthalmitis

Chiquet, C., Cornut, P., Benito, Y., et al. (2008) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.07-1377 · Cited by 141 · see citing works

Role of Neurotrophin Receptor TrkB in the Maturation of Rod Photoreceptors and Establishment of Synaptic Transmission to the Inner Retina

Rohrer, B., Korenbrot, J. I., LaVail, M. M., Reichardt, L. F., & Xu, B. (1999) · Journal of Neuroscience · doi:10.1523/jneurosci.19-20-08919.1999 · Cited by 137 · see citing works

Relationship between Muller cell responses, a local transretinal potential, and potassium flux

Karowski, C. J., & Proenza, L. M. (1977) · Journal of Neurophysiology · doi:10.1152/jn.1977.40.2.244 · Cited by 137 · see citing works

Survival of Purified Rat PhotoreceptorsIn VitroIs Stimulated Directly by Fibroblast Growth Factor-2

Fontaine, V., Kinkl, N., Sahel, J., et al. (1998) · Journal of Neuroscience · doi:10.1523/jneurosci.18-23-09662.1998 · Cited by 135 · see citing works

Toll-like receptor 2-mediated expression of β-defensin-2 in human corneal epithelial cells

Kumar, A., Zhang, J., & Yu, F. X. (2005) · Microbes and Infection · doi:10.1016/j.micinf.2005.07.006 · Cited by 132 · see citing works

Norrin Mediates Neuroprotective Effects on Retinal Ganglion Cells via Activation of the Wnt/β-Catenin Signaling Pathway and the Induction of Neuroprotective Growth Factors in Müller Cells

Seitz, R., Hackl, S., Seibuchner, T., Tamm, E. R., & Ohlmann, A. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.0730-10.2010 · Cited by 131 · see citing works

The role of glia in retinal vascular disease

Coorey, N. J., Shen, W., Chung, S. H., Zhu, L., & Gillies, M. C. (2012) · Clinical and Experimental Optometry · doi:10.1111/j.1444-0938.2012.00741.x · Cited by 130 · see citing works

Advanced glycation end products increase endothelial permeability through the RAGE/Rho signaling pathway

Hirose, A., Tanikawa, T., Mori, H., Okada, Y., & Tanaka, Y. (2010) · FEBS Letters · doi:10.1016/j.febslet.2009.11.082 · Cited by 129 · see citing works

Müller cell protection of rat retinal ganglion cells from glutamate and nitric oxide neurotoxicity.

Kawasaki, A., Otori, Y., & Barnstable, C. J. (2000) · PubMed · Cited by 125 · see citing works

Cytokine-mediated activation of a neuronal retinal resident cell provokes antigen presentation.

Percopo, C. M., Hooks, J. J., Shinohara, T., Caspi, R. R., & Detrick, B. (1990) · The Journal of Immunology · doi:10.4049/jimmunol.145.12.4101 · Cited by 124 · see citing works

Toll-Like Receptors and Corneal Innate Immunity

Kumar, A., & Yu, F.-S. (2006) · Current Molecular Medicine · doi:10.2174/156652406776894572 · Cited by 120 · see citing works

Role of Müller glia in neuroprotection and regeneration in the retina.

García, M., & Vecino, E. (2003) · PubMed · doi:10.14670/hh-18.1205 · Cited by 119 · see citing works

The inhibitor of phagocytosis, O-phospho-l-serine, suppresses Müller glia proliferation and cone cell regeneration in the light-damaged zebrafish retina

Bailey, T. J., Fossum, S. L., Fimbel, S. M., Montgomery, J. E., & Hyde, D. R. (2010) · Experimental Eye Research · doi:10.1016/j.exer.2010.07.017 · Cited by 117 · see citing works

Cellular and Subcellular Patterns of Expression of bFGF and CNTF in the Normal and Light Stressed Adult Rat Retina

Walsh, N., Valter, K., & Stone, J. (2001) · Experimental Eye Research · doi:10.1006/exer.2000.0984 · Cited by 115 · see citing works

Potential role of glial cell line-derived neurotrophic factor receptors in Müller glial cells during light-induced retinal degeneration

Harada, C., Harada, T., Quah, H.-M. A., Maekawa, F., Yoshida, K., Ohno, S., Wada, K., Parada, L. F., & Tanaka, K. (2003) · Neuroscience · doi:10.1016/s0306-4522(03)00599-2 · Cited by 113 · see citing works

Glutamate stimulates neurotrophin expression in cultured Müller cells

Taylor, S. C., Srinivasan, B., Wordinger, R. J., & Roque, R. S. (2003) · Molecular Brain Research · doi:10.1016/s0169-328x(03)00030-5 · Cited by 105 · see citing works

Injury-independent induction of reactive gliosis in retina by loss of function of the LIM homeodomain transcription factor Lhx2

de Melo, J., Miki, K., Rattner, A., Smallwood, P. M., Zibetti, C., Hirokawa, K. E., Monuki, E. S., Campochiaro, P. A., & Blackshaw, S. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1107488109 · Cited by 101 · see citing works

Antisense knockdown of GLAST, a glial glutamate transporter, compromises retinal function.

Barnett, N. L., & Pow, D. V. (2000) · PubMed · Cited by 100 · see citing works

Immune regulation and the eye.

Stein-Streilein, J. (2008) · Trends in Immunology · doi:10.1016/j.it.2008.08.002 · Cited by 99 · see citing works

Microglial response to light‐induced photoreceptor degeneration in the mouse retina

Santos, A. M., Martín‐Oliva, D., Ferrer‐Martín, R. M., Tassi, M., Calvente, R., Sierra, A., Carrasco, M., Marín‐Teva, J. L., Navascués, J., & Cuadros, M. Á. (2009) · The Journal of Comparative Neurology · doi:10.1002/cne.22227 · Cited by 97 · see citing works

INFECTIOUS ENDOPHTHALMITIS AFTER INTRAVITREAL INJECTION OF ANTIANGIOGENIC AGENTS

Diago, T., McCannel, C. A., Bakri, S. J., Pulido, J. S., Edwards, A. O., & Pach, J. M. (2009) · Retina · doi:10.1097/iae.0b013e31819d2591 · Cited by 96 · see citing works

Retinal Muller Glia Initiate Innate Response to Infectious Stimuli via Toll-Like Receptor Signaling

Kumar, A., & Shamsuddin, N. (2012) · PLoS ONE · doi:10.1371/journal.pone.0029830 · Cited by 91 · see citing works

Microglia-Mediated IGF-I Neuroprotection in the rd10 Mouse Model of Retinitis Pigmentosa

Arroba, A. I., Álvarez-Lindo, N., van Rooijen, N., & de la Rosa, E. J. (2011) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.11-7736 · Cited by 86 · see citing works

Toll-Like Receptor 2 Ligand Pretreatment Attenuates Retinal Microglial Inflammatory Response but Enhances Phagocytic Activity toward Staphylococcus aureus

Kochan, T. J., Singla, A., Tosi, J., & Kumar, A. (2012) · Infection and Immunity · doi:10.1128/iai.00149-12 · Cited by 81 · see citing works

Early postnatal Müller cell death leads to retinal but not optic nerve degeneration in NSE-Hu-Bcl-2 transgenic mice

Dubois‐Dauphin, M., Poitry-Yamate, C., de Bilbao, F., et al. (1999) · Neuroscience · doi:10.1016/s0306-4522(99)00313-9 · Cited by 81 · see citing works

Bacterial endophthalmitis in the age of outpatient intravitreal therapies and cataract surgeries: Host–microbe interactions in intraocular infection

Sadaka, A., Durand, M. L., & Gilmore, M. S. (2012) · Progress in Retinal and Eye Research · doi:10.1016/j.preteyeres.2012.03.004 · Cited by 79 · see citing works

Endocannabinoids alleviate proinflammatory conditions by modulating innate immune response in muller glia during inflammation

Krishnan, G., & Chatterjee, N. (2012) · Glia · doi:10.1002/glia.22380 · Cited by 77 · see citing works

Evidence for glutamate-mediated excitotoxic mechanisms during photoreceptor degeneration in the rd1 mouse retina.

Delyfer, M., Forster, V., Neveux, N., et al. (2005) · PubMed · Cited by 77 · see citing works

Antibiotic sensitivity profile of bacterial pathogens in postoperative wound infections at a tertiary care hospital in Gujarat, India

Goswami, N. N., Trivedi, H. R., Goswami, A., et al. (2011) · Journal of Pharmacology and Pharmacotherapeutics · doi:10.4103/0976-500x.83279 · Cited by 77 · see citing works

Fibroblast growth factor phosphorylation and receptors in rod outer segments.

Mascarelli, F., Raulais, D., & Courtois, Y. (1989) · The EMBO Journal · doi:10.1002/j.1460-2075.1989.tb08351.x · Cited by 76 · see citing works

The immunomodulating neuropeptide alpha-melanocyte-stimulating hormone (α-MSH) suppresses LPS-stimulated TLR4 with IRAK-M in macrophages

Taylor, A. W. (2005) · Journal of Neuroimmunology · doi:10.1016/j.jneuroim.2005.01.008 · Cited by 75 · see citing works

Novel Role for the Innate Immune Receptor Toll-Like Receptor 4 (TLR4) in the Regulation of the Wnt Signaling Pathway and Photoreceptor Apoptosis

Yi, H., Patel, A. K., Sodhi, C. P., et al. (2012) · PLoS ONE · doi:10.1371/journal.pone.0036560 · Cited by 74 · see citing works

αB-Crystallin Protects Retinal Tissue during Staphylococcus aureus - Induced Endophthalmitis

Whiston, E., Sugi, N., Kamradt, M. C., Sack, C. S., Heimer, S. R., Engelbert, M., Wawrousek, E. F., Gilmore, M. S., Ksander, B. R., & Gregory, M. S. (2008) · Infection and Immunity · doi:10.1128/iai.01285-07 · Cited by 72 · see citing works

Visual Outcome and Bacterial Sensitivity After Methicillin-Resistant Staphylococcus aureus–Associated Acute Endophthalmitis

DERAMO, V. A., Lai, J. C., Winokur, J. A., et al. (2008) · American Journal of Ophthalmology · doi:10.1016/j.ajo.2007.10.020 · Cited by 68 · see citing works

Time Course of Neurotrophic Factor Upregulation and Retinal Protection against Light-Induced Damage after Optic Nerve Section

Valter, K., Bisti, S., Gargini, C., Loreto, S. D., Maccarone, R., Cervetto, L., & Stone, J. (2005) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.04-0657 · Cited by 66 · see citing works

Staphylococcus aureus lipoproteins trigger human corneal epithelial innate response through toll-like receptor-2

Li, Q., Kumar, A., Gui, J., & Yu, F. X. (2007) · Microbial Pathogenesis · doi:10.1016/j.micpath.2007.11.006 · Cited by 66 · see citing works

Toll‐like Receptor 2 Ligand–Induced Protection against Bacterial Endophthalmitis

Kumar, A., Singh, C. N., Glybina, I. V., Mahmoud, T. H., & Yu, F. X. (2009) · The Journal of Infectious Diseases · doi:10.1086/649589 · Cited by 66 · see citing works

TLR2 Mediates the Innate Response of Retinal Muller Glia to Staphylococcus aureus

Shamsuddin, N., & Kumar, A. (2011) · The Journal of Immunology · doi:10.4049/jimmunol.1100565 · Cited by 66 · see citing works

l-Glutamate conditionally modulates the K+ current of miller glial cells

Schwartz, E. A. (1993) · Neuron · doi:10.1016/0896-6273(93)90062-v · Cited by 65 · see citing works

Regulation of eye derived growth factor binding to membranes by light, ATP or GTP in photoreceptor outer segments.

Plouët, J., Mascarelli, F., Loret, M. D., et al. (1988) · The EMBO Journal · doi:10.1002/j.1460-2075.1988.tb02823.x · Cited by 62 · see citing works

Endophthalmitis After Anti-VEGF Injections

Klein, K. S., Walsh, M. K., Hassan, T., et al. (2009) · Ophthalmology · doi:10.1016/j.ophtha.2009.02.031 · Cited by 60 · see citing works

Phagocytosis by human retinal glial cells in culture.

Mano, T., & Puro, D. G. (1990) · PubMed · Cited by 58 · see citing works

Expression of human beta-defensins in intraocular tissues.

Haynes, R. J., McElveen, J. E., Dua, H. S., Tighe, P. J., & Liversidge, J. (2000) · PubMed · Cited by 56 · see citing works

Colocalization of TrkB and brain-derived neurotrophic factor proteins in green-red-sensitive cone outer segments.

Polo, A. D., Cheng, L., Bray, G. M., & Aguayo, A. J. (2000) · PubMed · Cited by 55 · see citing works

gamma-Aminobutyric acid (GABA)-induced currents of skate Muller (glial) cells are mediated by neuronal-like GABAA receptors.

Malchow, R. P., Qian, H., & Ripps, H. (1989) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.86.11.4326 · Cited by 53 · see citing works

Calcium waves in dissociated retinal glial (Müller) cells are evoked by release of calcium from intracellular stores

Keirstead, S. A., & Miller, R. F. (1995) · Glia · doi:10.1002/glia.440140104 · Cited by 52 · see citing works

Fas Ligand but Not Complement Is Critical for Control of Experimental Staphylococcus aureus Endophthalmitis

Engelbert, M., & Gilmore, M. S. (2005) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.04-1139 · Cited by 52 · see citing works

Ciliary neurotrophic factor induces glial fibrillary acidic protein in retinal Müller cells through the JAK/STAT signal transduction pathway

Wang, Y., Smith, S. B., Ogilvie, J. M., McCool, D. J., & Sarthy, V. P. (2002) · Current Eye Research · doi:10.1076/ceyr.24.4.305.8408 · Cited by 50 · see citing works

Ciliary Neurotrophic Factor Induces Genes Associated with Inflammation and Gliosis in the Retina: A Gene Profiling Study of Flow-Sorted, Müller Cells

Xue, W., Cojocaru, R. I., Dudley, V. J., Brooks, M., Swaroop, A., & Sarthy, V. P. (2011) · PLoS ONE · doi:10.1371/journal.pone.0020326 · Cited by 49 · see citing works

Characterization of Wnt Signaling during Photoreceptor Degeneration

Yi, H., Nakamura, R. E. I., Mohamed, O. A., Dufort, D., & Hackam, A. S. (2007) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.07-0097 · Cited by 48 · see citing works

Role of the low-affinity NGF receptor (p75) in survival of retinal bipolar cells

Wexler, E., BERKOVICH, O., & Nawy, S. (1998) · Visual Neuroscience · doi:10.1017/s095252389815201x · Cited by 48 · see citing works

Neurotrophic Factor Receptors in Epiretinal Membranes After Human Diabetic Retinopathy

Harada, T., Harada, C., Mitamura, Y., et al. (2002) · Diabetes Care · doi:10.2337/diacare.25.6.1060 · Cited by 45 · see citing works

A physiological measure of carbonic anhydrase in müller cells

Newman, E. A. (1994) · Glia · doi:10.1002/glia.440110402 · Cited by 45 · see citing works

Reduced Nitro-oxidative Stress and Neural Cell Death Suggests a Protective Role for Microglial Cells in TNFα −/− Mice in Ischemic Retinopathy

Stevenson, L., Matesanz, N., Colhoun, L. M., Edgar, K. S., Devine, A. B., Gardiner, T. A., & McDonald, D. (2010) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.09-4344 · Cited by 43 · see citing works

Fibroblast Growth Factor Receptor 4 (FGFR4) Is Expressed in Adult Rat and Human Retinal Photoreceptors and Neurons

Fuhrmann, V., Kinkl, N., Léveillard, T., et al. (1999) · Journal of Molecular Neuroscience · doi:10.1385/jmn:13:1-2:187 · Cited by 43 · see citing works

Location of CNTFRα on outer segments: evidence of the site of action of CNTF in rat retina

Valter, K., Bisti, S., & Stone, J. (2003) · Brain Research · doi:10.1016/s0006-8993(03)03130-5 · Cited by 41 · see citing works

Immunolocalization of basic fibroblast growth factor and its receptor in adult goldfish retina

Raymond, P. A., Barthel, L. K., & Rounsifer, M. E. (1992) · Experimental Neurology · doi:10.1016/0014-4886(92)90225-f · Cited by 40 · see citing works

Bacillus cereusInduces Permeability of an In Vitro Blood-Retina Barrier

Moyer, A. L., Ramadan, R. T., Thurman, J. M., Burroughs, A. M., & Callegan, M. C. (2008) · Infection and Immunity · doi:10.1128/iai.01330-07 · Cited by 38 · see citing works

Fibroblast growth factor receptor (FGFR) and candidate signaling molecule distribution within rat and human retina.

Kinkl, N., Hageman, G. S., Sahel, J., et al. (2002) · PubMed · Cited by 37 · see citing works

Regulatory Role of TLR Ligands on the Activation of Autoreactive T Cells by Retinal Astrocytes

Jiang, G., Yan, K., Sun, D., Wang, Y., Kaplan, H. J., & Shao, H. (2009) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.08-3303 · Cited by 37 · see citing works

The Wnt Signaling Pathway Protects Retinal Ganglion Cell 5 (RGC-5) Cells from Elevated Pressure

Fragoso, M. A., Yi, H., Nakamura, R. E. I., et al. (2010) · Cellular and Molecular Neurobiology · doi:10.1007/s10571-010-9603-z · Cited by 34 · see citing works

The Diabetic Ocular Environment Facilitates the Development of Endogenous Bacterial Endophthalmitis

Coburn, P. S., Wiskur, B. J., Christy, E., et al. (2012) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.12-10661 · Cited by 34 · see citing works

Toward Improving Therapeutic Regimens for Bacillus Endophthalmitis

Wiskur, B. J., Robinson, M. L., Farrand, A. J., Novosad, B. D., & Callegan, M. C. (2008) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.07-1303 · Cited by 34 · see citing works

NOD1 Expression in the Eye and Functional Contribution to IL-1β–Dependent Ocular Inflammation in Mice

Rosenzweig, H. L., Galster, K. T., Planck, S. R., & Rosenbaum, J. T. (2009) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.08-2852 · Cited by 34 · see citing works

Neurotrophin receptors (Trk A, Trk B, and Trk C) in the developing and adult human retina

Nag, T. C., & Wadhwa, S. (1999) · Developmental Brain Research · doi:10.1016/s0165-3806(99)00121-2 · Cited by 32 · see citing works

Cytosolic calcium transient increase through the AMPA/kainate receptor in cultured Müller cells

Wakakura, M., & Yamamoto, N. (1994) · Vision Research · doi:10.1016/0042-6989(94)90293-3 · Cited by 31 · see citing works

Müller glial cells of the tree shrew retina

Reichenbach, A., Frömter, C., Engelmann, R., Wolburg, H., Kasper, M. E., & Schnitzer, J. (1995) · The Journal of Comparative Neurology · doi:10.1002/cne.903600205 · Cited by 30 · see citing works

The immune response and the eye. I. The effects of monoclonal antibodies to T suppressor factors in anterior chamber-associated immune deviation (ACAID).

Ferguson, T. A., & Kaplan, H. J. (1987) · The Journal of Immunology · doi:10.4049/jimmunol.139.2.346 · Cited by 28 · see citing works

Distribution and development of nicotinic acetylcholine receptor subtypes in the optic tectum ofRana pipiens

Butt, C. M., Pauly, J. R., & Debski, E. A. (2000) · The Journal of Comparative Neurology · doi:10.1002/1096-9861(20000807)423:4 · Cited by 22 · see citing works

Norrin attenuates protease-mediated death of transformed retinal ganglion cells.

Lin, S., Cheng, M., Dailey, W., et al. (2009) · PubMed · Cited by 20 · see citing works

GABAA receptor currents recorded from Müller glial cells of the baboon (Papio cynocephalus) retina

Reichelt, W., Hernández, M. D., Damian, R. T., et al. (1996) · Neuroscience Letters · doi:10.1016/0304-3940(95)12281-8 · Cited by 20 · see citing works

Treatment of Experimental Bacillus cereus Endophthalmitis Using Intravitreal Moxifloxacin With or Without Dexamethasone

Şakalar, Y. B., Ozekinci, S. O., & Çelen, M. K. (2011) · Journal of Ocular Pharmacology and Therapeutics · doi:10.1089/jop.2011.0021 · Cited by 12 · see citing works

Wnt14 inhibits death of retinal precursor cells

Mizukami, M., Souchelnytskyi, N., Kiuchi, Y., et al. (2009) · Experimental Eye Research · doi:10.1016/j.exer.2009.04.011 · Cited by 9 · see citing works

MRSA and cataract surgery – reflections for practice

Porter, L. F. (2010) · Clinical ophthalmology · doi:10.2147/opth.s12027 · Cited by 9 · see citing works

[Expression of basic fibroblast growth factor and fibroblast growth factor receptor 1 in the experimental retinal vein occlusion model].

Matsushima, M., Yamada, H., Yamamoto, C., et al. (1997) · PubMed · Cited by 4 · see citing works

Risk mitigation of immunogenicity: a key to personalized retinal gene therapy

Varin, J., Morival, C., Maillard, N., Adjali, O., & Cronin, T. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms222312818 · Cited by 19 · see citing works

Retina regeneration in zebrafish

Wan, J., & Goldman, D. J. (2016) · Current Opinion in Genetics & Development · doi:10.1016/j.gde.2016.05.009 · Cited by 247 · see citing works

Role of Müller glia in neuroprotection and regeneration in the retina.

García, M., & Vecino, E. (2003) · PubMed · doi:10.14670/hh-18.1205 · Cited by 119 · see citing works

Comparative proteomic analysis of normal and gliotic PVR retina and contribution of Müller glia to this profile

Eastlake, K., Heywood, W., Banerjee, P., Bliss, E., Mills, K. A., Khaw, P. T., Charteris, D. G., & Limb, G. A. (2018) · Experimental Eye Research · doi:10.1016/j.exer.2018.08.016 · Cited by 21 · see citing works

Reloading the retina by modifying the glial matrix

Quinlan, R. A., & Nilsson, M. (2004) · Trends in Neurosciences · doi:10.1016/j.tins.2004.02.009 · Cited by 17 · see citing works

Expression of glia maturation factor during retinal development in the rat

Nishiwaki, A., Asai, K., Tada, T., Ueda, T., Shimada, S., Ogura, Y., & Kato, T. (2001) · Molecular Brain Research · doi:10.1016/s0169-328x(01)00252-2 · Cited by 24 · see citing works