Characterization of green fluorescent protein-expressing retinal cone bipolar cells in a 5-hydroxytryptamine receptor 2a transgenic mouse line

Neuroscience

Volumn 163, Issue 2, 2009, Pages 662-668

  Lu, Q ^a   Ivanova, E ^a   Pan, Z H ^a  

^a WAYNE STATE UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

5 HTR2a EGFP; green fluorescent protein; immunostaining; retina; transgenic mouse; type 4 cone bipolar cell

Indexed keywords

GREEN FLUORESCENT PROTEIN; MOLECULAR MARKER; SEROTONIN 2A RECEPTOR;

ANIMAL CELL; ANIMAL TISSUE; ARTICLE; CELL DENSITY; CELL FUNCTION; CELL LABELING; CELL POPULATION; CELL STRUCTURE; CONTROLLED STUDY; DISEASE SEVERITY; GENE MUTATION; IMMUNOHISTOCHEMISTRY; MOUSE; NONHUMAN; PERINATAL PERIOD; PRIORITY JOURNAL; PROTEIN EXPRESSION; RETINA BIPOLAR GANGLION CELL; RETINA CONE; RETINA DEGENERATION; TRANSGENIC MOUSE;

AGING; ANIMALS; CELL COUNT; CHOLINE O-ACETYLTRANSFERASE; GREEN FLUORESCENT PROTEINS; IMMUNOHISTOCHEMISTRY; KV CHANNEL-INTERACTING PROTEINS; MICE; MICE, TRANSGENIC; RECEPTOR, SEROTONIN, 5-HT2A; RECOVERIN; RETINA; RETINAL BIPOLAR CELLS;

EID: 69249217792     PISSN: 03064522     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.neuroscience.2009.07.002     Document Type: Article

References (39)

1. Bowes C., Li T., Danciger M., Baxter L.C., Applebury M.L., and Farber D.B. Retinal degeneration in the rd mouse is caused by a defect in the beta subunit of rod cGMP-phosphodiesterase. Nature 347 (1990) 677-680
2. Boycott B.B., and Dowling J.E. Organization of the primate retina: light microscopy. Philos Trans R Soc Lond B Biol Sci 255 (1969) 109-184
3. Boycott B.B., and Kolb H. The connections between the bipolar cells and photoreceptors in the retina of the domestic cat. J Comp Neurol 148 (1973) 91-114
4. Dacheux R.F., and Raviola E. The rod pathway in the rabbit retina: a depolarizing bipolar and amacrine cell. J Neurosci 6 (1986) 331-345
5. DeVries S.H. Bipolar cells use kainate and AMPA receptors to filter visual information into separate channels. Neuron 28 (2000) 847-856
6. Dhingra A., Sulaiman P., Xu Y., Fina M.E., Veh R.W., and Vardi N. Probing neurochemical structure and function of retinal ON bipolar cells with a transgenic mouse. J Comp Neurol 510 (2008) 484-496
7. Duebel J., Haverkamp S., Schleich W., Feng G., Augustine G.J., Kuner T., and Euler T. Two-photon imaging reveals somatodendritic chloride gradient in retinal ON-type bipolar cells expressing the biosensor clomeleon. Neuron 49 (2006) 81-94
8. Euler T., and Wässle H. Immunocytochemical identification of cone bipolar cells in the rat retina. J Comp Neurol 361 (1995) 461-478
9. Famiglietti E.V. Functional architecture of cone bipolar cells in mammalian retina. Vision Res 21 (1981) 1559-1564
10. Fox M.A., and Sanes J.R. Synaptotagmin I and II are present in distinct subsets of central synapses. J Comp Neurol 503 (2007) 280-296
11. Fyk-Kolodziej B., and Pourcho R.G. Differential distribution of hyperpolarization-activated and cyclic nucleotide-gated channels in cone bipolar cells of the rat retina. J Comp Neurol 501 (2007) 891-903
12. 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
13. Gong S., Zheng C., Doughty M.L., Losos K., Didkovsky N., Schambra U.B., Nowak N.J., Joyner A., Leblanc G., Hatten M.E., and Heintz N. A gene expression atlas of the central nervous system based on bacterial artificial chromosomes. Nature 425 (2003) 917-925
14. Han Y., and Massey S.C. Electrical synapses in retinal ON cone bipolar cells: subtype-specific expression of connexins. Proc Natl Acad Sci U S A 102 (2005) 13313-13318
15. Han L., Zhong Y.-M., and Yang X.-L. 5-HT2A receptors are differentially expressed in bullfrog and rat retinas: a comparative study. Brain Res Bull 73 (2007) 273-277
16. Haverkamp S., Ghosh K.K., Hirano A.A., and Wässle H. Immunocytochemical description of five bipolar cell types of the mouse retina. J Comp Neurol 455 (2003) 463-476
17. Haverkamp S., Specht D., Majumdar S., Zaidi N.F., Brandstätter J.H., Wasco W., Wässle H., and Tom Dieck S. Type 4 OFF cone bipolar cells of the mouse retina express calsenilin and contact cones as well as rods. J Comp Neurol 507 (2008) 1087-1101
18. Haverkamp S., Wässle H., Duebel J., Kuner T., Augustine G.J., Feng G., and Euler T. The primordial, blue cone color system of the mouse retina. J Neurosci 25 (2005) 5438-5445
19. Haverkamp S., Inta D., Monyer H., and Wässle H. Expression analysis of green fluorescent protein in retinal neurons of four transgenic mouse lines. Neuroscience 160 (2009) 126-139
20. + currents in mammalian retinal bipolar cells. Vis Neurosci 19 (2002) 163-173
21. Huang L., Max M., Margolskee R.F., Su H., Masland R.H., and Euler T. G protein subunit Gγ13 is coexpressed with Gαo, Gβ3, and Gβ4 in retinal ON bipolar cells. J Comp Neurol 455 (2003) 1-10
22. Ivanova E., and Müller F. Retinal bipolar cell types differ in their inventory of ion channels. Vis Neurosci 23 (2006) 143-154
23. Kolb H., Nelson R., and Mariani A. Amacrine cells, bipolar cells and ganglion cells of the cat retina: a Golgi study. Vision Res 21 (1981) 1081-1114
24. Lin B., Jakobs T.C., and Masland R.H. Different functional types of bipolar cells use different gap-junctional proteins. J Neurosci 25 (2005) 6696-6701
25. Lin B., and Masland R.H. Synaptic contacts between an identified type of ON cone bipolar cell and ganglion cells in the mouse retina. Eur J Neurosci 21 (2005) 1257-1270
26. + currents (IKir) with a different distribution than that of Ih. J Neurophysiol 90 (2003) 3479-3489
27. Mataruga A., Kremmer E., and Müller F. Type 3a and type 3b OFF cone bipolar cells provide for the alternative rod pathway in the mouse retina. J Comp Neurol 502 (2007) 1123-1137
28. Morgan J.L., Dhingra A., Vardi N., and Wong R.O. Axons and dendrites originate from neuroepithelial-like processes of retinal bipolar cells. Nat Neurosci 9 (2006) 85-92
29. Müller F., Scholten A., Ivanova E., Haverkamp S., Kremmer E., and Kaupp U.B. HCN channels are expressed differentially in retinal bipolar cells and concentrated at synaptic terminals. Eur J Neurosci 17 (2003) 2084-2096
30. Pan Z.-H. Differential expression of high- and two types of low-voltage-activated calcium currents in rod and cone bipolar cells of the rat retina. J Neurophysiol 83 (2000) 513-527
31. + currents in mammalian retinal cone bipolar cells. J Neurophysiol 84 (2000) 2564-2571
32. Pignatelli V., and Strettoi E. Bipolar cells of the mouse retina: a gene gun, morphological study. J Comp Neurol 476 (2004) 254-266
33. Pootanakit K., Prior K.J., Hunter D.D., and Brunken W.J. 5-HT2a receptors in the rabbit retina: potential presynaptic modulators. Vis Neurosci 16 (1999) 221-230
34. Pourcho R.G., and Goebel D.J. A combined Golgi and autoradiographic study of 3H-glycine-accumulating cone bipolar cells in the cat retina. J Neurosci 7 (1987) 1178-1188
35. Strettoi E., and Pignatelli V. Modifications of retinal neurons in a mouse model of retinitis pigmentosa. Proc Natl Acad Sci U S A 97 (2000) 11020-11025
36. Wässle H. Parallel processing in the mammalian retina. Nat Rev Neurosci 5 (2004) 747-757
37. Wässle H., Puller C., Müller F., and Haverkamp S. Cone contacts, mosaics, and territories of bipolar cells in the mouse retina. J Neurosci 29 (2009) 106-117
38. Wong G.T., Ruiz-Avila L., and Margolskee R.F. Directing gene expression to gustducin-positive taste receptor cells. J Neurosci 19 (1999) 5802-5809
39. Wu S.M., Gao F., and Maple B.R. Functional architecture of synapses in the inner retina: segregation of visual signals by stratification of bipolar cell axon terminals. J Neurosci 20 (2000) 4462-4470