Local Retinal Circuits of Melanopsin-Containing Ganglion Cells Identified by Transsynaptic Viral Tracing

Current Biology

Volumn 17, Issue 11, 2007, Pages 981-988

  Viney, Tim James ^a   Balint, Kamill ^a,f   Hillier, Daniel ^a,c   Siegert, Sandra ^a   Boldogkoi, Zsolt ^f   Enquist, Lynn W ^d   Meister, Markus ^b   Cepko, Constance L ^e   Roska, Botond ^a,b,e  

^a FRIEDRICH MIESCHER INSTITUTE FOR BIOMEDICAL RESEARCH   (Switzerland)

^b HARVARD UNIVERSITY   (United States)

^c PÁZMÁNY PÉTER CATHOLIC UNIVERSITY   (Hungary)

^d PRINCETON UNIVERSITY   (United States)

^e HARVARD MEDICAL SCHOOL   (United States)

^f UNIVERSITY OF SZEGED   (Hungary)

Author keywords

SYSNEURO

Indexed keywords

GREEN FLUORESCENT PROTEIN; MELANOPSIN; OPSIN;

ANIMAL; ARTICLE; GENETICS; METABOLISM; MOUSE; PHYSIOLOGY; PSEUDORABIES HERPETOVIRUS; RADIATION EXPOSURE; RETINA AMACRINE CELL; RETINA GANGLION CELL; SYNAPTIC TRANSMISSION; VIROLOGY; VISUAL SYSTEM;

AMACRINE CELLS; ANIMALS; GREEN FLUORESCENT PROTEINS; HERPESVIRUS 1, SUID; MICE; OPSIN; RETINAL GANGLION CELLS; SYNAPTIC TRANSMISSION; VISUAL PATHWAYS;

SUID HERPESVIRUS 1;

EID: 34249666623     PISSN: 09609822     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.cub.2007.04.058     Document Type: Article

References (43)

1. Fu Y., Liao H.W., Do M.T., and Yau K.W. Non-image-forming ocular photoreception in vertebrates. Curr. Opin. Neurobiol. 15 (2005) 415-422
2. Belenky M.A., Smeraski C.A., Provencio I., Sollars P.J., and Pickard G.E. Melanopsin retinal ganglion cells receive bipolar and amacrine cell synapses. J. Comp. Neurol. 460 (2003) 380-393
3. Dacey D.M., Liao H.W., Peterson B.B., Robinson F.R., Smith V.C., Pokorny J., Yau K.W., and Gamlin P.D. Melanopsin-expressing ganglion cells in primate retina signal colour and irradiance and project to the LGN. Nature 433 (2005) 749-754
4. Sollars P.J., Smeraski C.A., Kaufman J.D., Ogilvie M.D., Provencio I., and Pickard G.E. Melanopsin and non-melanopsin expressing retinal ganglion cells innervate the hypothalamic suprachiasmatic nucleus. Vis. Neurosci. 20 (2003) 601-610
5. Card J.P. Pseudorabies virus and the functional architecture of the circadian timing system. J. Biol. Rhythms 15 (2000) 453-461
6. Jons A., and Mettenleiter T.C. Green fluorescent protein expressed by recombinant pseudorabies virus as an in vivo marker for viral replication. J. Virol. Methods 66 (1997) 283-292
7. Smith B.N., Banfield B.W., Smeraski C.A., Wilcox C.L., Dudek F.E., Enquist L.W., and Pickard G.E. Pseudorabies virus expressing enhanced green fluorescent protein: A tool for in vitro electrophysiological analysis of transsynaptically labeled neurons in identified central nervous system circuits. Proc. Natl. Acad. Sci. USA 97 (2000) 9264-9269
8. Boldogkoi Z., Erdelyi F., Sik A., Freund T.F., and Fodor I. Construction of a recombinant herpesvirus expressing the jellyfish green fluorescent protein. Luminescence 14 (1999) 69-74
9. Boldogkoi Z., Reichart A., Toth I.E., Sik A., Erdelyi F., Medveczky I., Llorens-Cortes C., Palkovits M., and Lenkei Z. Construction of recombinant pseudorabies viruses optimized for labeling and neurochemical characterization of neural circuitry. Brain Res. Mol. Brain Res. 109 (2002) 105-118
10. Yoon H., Enquist L.W., and Dulac C. Olfactory inputs to hypothalamic neurons controlling reproduction and fertility. Cell 123 (2005) 669-682
11. DeFalco J., Tomishima M., Liu H., Zhao C., Cai X., Marth J.D., Enquist L., and Friedman J.M. Virus-assisted mapping of neural inputs to a feeding center in the hypothalamus. Science 291 (2001) 2608-2613
12. Pomeranz L.E., Reynolds A.E., and Hengartner C.J. Molecular biology of pseudorabies virus: Impact on neurovirology and veterinary medicine. Microbiol. Mol. Biol. Rev. 69 (2005) 462-500
13. Pickard G.E., Smeraski C.A., Tomlinson C.C., Banfield B.W., Kaufman J., Wilcox C.L., Enquist L.W., and Sollars P.J. Intravitreal injection of the attenuated pseudorabies virus PRV Bartha results in infection of the hamster suprachiasmatic nucleus only by retrograde transsynaptic transport via autonomic circuits. J. Neurosci. 22 (2002) 2701-2710
14. Smeraski C.A., Sollars P.J., Ogilvie M.D., Enquist L.W., and Pickard G.E. Suprachiasmatic nucleus input to autonomic circuits identified by retrograde transsynaptic transport of pseudorabies virus from the eye. J. Comp. Neurol. 471 (2004) 298-313
15. Coombs J., van der List D., Wang G.Y., and Chalupa L.M. Morphological properties of mouse retinal ganglion cells. Neuroscience 140 (2006) 123-136 10.1016/j.neuroscience.2006.02.079 Published online June 19, 2006
16. Sun W., Li N., and He S. Large-scale morphological survey of mouse retinal ganglion cells. J. Comp. Neurol. 451 (2002) 115-126
17. Kong J.H., Fish D.R., Rockhill R.L., and Masland R.H. Diversity of ganglion cells in the mouse retina: Unsupervised morphological classification and its limits. J. Comp. Neurol. 489 (2005) 293-310
18. Masland R.H. The fundamental plan of the retina. Nat. Neurosci. 4 (2001) 877-886
19. Wassle H. Parallel processing in the mammalian retina. Nat. Rev. Neurosci. 5 (2004) 747-757
20. Haverkamp S., and Wässle H. Immunocytochemical analysis of the mouse retina. J. Comp. Neurol. 424 (2000) 1-23
21. Card J.P., Whealy M.E., Robbins A.K., Moore R.Y., and Enquist L.W. Two alpha-herpesvirus strains are transported differentially in the rodent visual system. Neuron 6 (1991) 957-969
22. Hattar S., Kumar M., Park A., Tong P., Tung J., Yau K.W., and Berson D.M. Central projections of melanopsin-expressing retinal ganglion cells in the mouse. J. Comp. Neurol. 497 (2006) 326-349
23. Hannibal J., and Fahrenkrug J. Target areas innervated by PACAP-immunoreactive retinal ganglion cells. Cell Tissue Res. 316 (2004) 99-113
24. Sekaran S., Foster R.G., Lucas R.J., and Hankins M.W. Calcium imaging reveals a network of intrinsically light-sensitive inner-retinal neurons. Curr. Biol. 13 (2003) 1290-1298
25. Hattar S., Liao H.W., Takao M., Berson D.M., and Yau K.W. Melanopsin-containing retinal ganglion cells: Architecture, projections, and intrinsic photosensitivity. Science 295 (2002) 1065-1070
26. Ghosh K.K., Bujan S., Haverkamp S., Feigenspan A., and Wässle H. Types of bipolar cells in the mouse retina. J. Comp. Neurol. 469 (2004) 70-82
27. Connaughton V.P., Graham D., and Nelson R. Identification and morphological classification of horizontal, bipolar, and amacrine cells within the zebrafish retina. J. Comp. Neurol. 477 (2004) 371-385
28. Famiglietti Jr. E.V., and Kolb H. Structural basis for ON-and OFF-center responses in retinal ganglion cells. Science 194 (1976) 193-195
29. Roska B., and Werblin F. Vertical interactions across ten parallel, stacked representations in the mammalian retina. Nature 410 (2001) 583-587
30. Gustincich S., Feigenspan A., Wu D.K., Koopman L.J., and Raviola E. Control of dopamine release in the retina: A transgenic approach to neural networks. Neuron 18 (1997) 723-736
31. Dowling J.E., and Ehinger B. Synaptic organization of the amine-containing interplexiform cells of the goldfish and Cebus monkey retinas. Science 188 (1975) 270-273
32. Marc R.E., and Liu W.L. Horizontal cell synapses onto glycine-accumulating interplexiform cells. Nature 312 (1984) 266-269
33. Mangel S.C., and Dowling J.E. Responsiveness and receptive field size of carp horizontal cells are reduced by prolonged darkness and dopamine. Science 229 (1985) 1107-1109
34. Lasater E.M., and Dowling J.E. Dopamine decreases conductance of the electrical junctions between cultured retinal horizontal cells. Proc. Natl. Acad. Sci. USA 82 (1985) 3025-3029
35. Witkovsky P. Dopamine and retinal function. Doc. Ophthalmol. 108 (2004) 17-40
36. Puopolo M., Hochstetler S.E., Gustincich S., Wightman R.M., and Raviola E. Extrasynaptic release of dopamine in a retinal neuron: Activity dependence and transmitter modulation. Neuron 30 (2001) 211-225
37. Contini M., and Raviola E. GABAergic synapses made by a retinal dopaminergic neuron. Proc. Natl. Acad. Sci. USA 100 (2003) 1358-1363
38. Sakamoto K., Liu C., Kasamatsu M., Pozdeyev N.V., Iuvone P.M., and Tosini G. Dopamine regulates melanopsin mRNA expression in intrinsically photosensitive retinal ganglion cells. Eur. J. Neurosci. 22 (2005) 3129-3136
39. Sakamoto K., Liu C., and Tosini G. Classical photoreceptors regulate melanopsin mRNA levels in the rat retina. J. Neurosci. 24 (2004) 9693-9697
40. Doi M., Yujnovsky I., Hirayama J., Malerba M., Tirotta E., Sassone-Corsi P., and Borrelli E. Impaired light masking in dopamine D2 receptor-null mice. Nat. Neurosci. 9 (2006) 732-734
41. Steenhard B.M., and Besharse J.C. Phase shifting the retinal circadian clock: xPer2 mRNA induction by light and dopamine. J. Neurosci. 20 (2000) 8572-8577
42. Hannibal J., Hindersson P., Knudsen S.M., Georg B., and Fahrenkrug J. The photopigment melanopsin is exclusively present in pituitary adenylate cyclase-activating polypeptide-containing retinal ganglion cells of the retinohypothalamic tract. J. Neurosci. 22 (2002) RC191
43. Franklin K., and Paxinos G. The Mouse Brain in Stereotaxic Coordinates. (1997), Academic Press, San Diego, California