Changing coupling pattern of The ON-OFF direction-selective ganglion cells in early postnatal mouse retina

Neuroscience

Volumn 250, Issue , 2013, Pages 798-808

  Xu, Z ^a,b   Zeng, Q ^a,b   Shi, X ^a,b   He, S ^c  

^a INSTITUTE OF BIOPHYSICS   (China)

^b UNIVERSITY OF CHINESE ACADEMY OF SCIENCES   (China)

^c SHANGHAI JIAO TONG UNIVERSITY   (China)

Author keywords

A (Ant); Cadherin 6; Cdh6; Col25 1; DSGC; EGTA; Gap junction; HEPES; I (Inf); Mouse; P (Post); PD; Retinal ganglion cell; S (Sup); SAC; Tracer coupling

Indexed keywords

CADHERIN; CADHERIN 6; GREEN FLUORESCENT PROTEIN; UNCLASSIFIED DRUG;

ANIMAL CELL; ARTICLE; CELL COUNT; CELL STRUCTURE; CELL TYPE; CONTROLLED STUDY; DEVELOPMENTAL STAGE; EYE MOVEMENT; IN SITU HYBRIDIZATION; MOUSE; NEWBORN; NONHUMAN; ON OFF DIRECTION SELECTIVE GANGLION CELL; POSTNATAL DEVELOPMENT; PRIORITY JOURNAL; PROTEIN EXPRESSION; RABBIT; RETINA GANGLION CELL;

4-(2-HYDROXYETHYL)-1-PIPERAZINEETHANESULFONIC ACID; A (ANT); ANTERIOR; CADHERIN-6; CDH6; COL25Α1; COLLAGEN25 ALPHA 1; DIRECTION SELECTIVE GANGLION CELL; DSGC; EGTA; ETHYLENE GLYCOL TETRAACETIC ACID; GAP JUNCTION; HEPES; I (INF); INFERIOR; MOUSE; P (POST); PD; POSTERIOR; PREFERRED DIRECTION; RETINAL GANGLION CELL; S (SUP); SAC; STARBURST AMACRINE CELL; SUPERIOR; TRACER COUPLING;

ALGORITHMS; ANIMALS; BIOTIN; DARKNESS; DATA INTERPRETATION, STATISTICAL; ELECTROPHYSIOLOGICAL PROCESSES; GREEN FLUORESCENT PROTEINS; IN SITU HYBRIDIZATION, FLUORESCENCE; MICE; MICE, INBRED C57BL; MICROSCOPY, FLUORESCENCE; PATCH-CLAMP TECHNIQUES; PHOTIC STIMULATION; RETINA; RETINAL GANGLION CELLS;

EID: 84884166420     PISSN: 03064522     EISSN: 18737544     Source Type: Journal    
DOI: 10.1016/j.neuroscience.2013.06.013     Document Type: Article

References (37)

1. Amthor F.R., Oyster C.W. Spatial organization of retinal information about the direction of image motion. Proc Natl Acad Sci U S A 1995, 92:4002-4005.
2. Beyer E., Paul D., Goodenough D. Connexin43: a protein from rat heart homologous to a gap junction protein from liver. J Cell Biol 1987, 105:2621-2629.
3. Chen M., Weng S., Deng Q., Xu Z., He S. Physiological properties of direction-selective ganglion cells in early postnatal and adult mouse retina. J Physiol 2009, 587:819-828.
4. Dahl G., Miller T., Paul D., Voellmy R., Werner R. Expression of functional cell-cell channels from cloned rat-liver gap junction complementary-DNA. Science 1987, 236:1290-1293.
5. DeBoer D.J., Vaney D.I. Gap-junction communication between subtypes of direction-selective ganglion cells in the developing retina. J Comp Neurol 2005, 482:85-93.
6. Dong W., Sun W., Zhang Y., Chen X., He S. Dendritic relationship between starburst amacrine cells and direction-selective ganglion cells in the rabbit retina. J Physiol 2004, 556:11-17.
7. Elfgang C., Eckert R., Lichtenberg-Frate H., Butterweck A., Traub O., Klein R.A., Hulser D.F., Willecke K. Specific permeability and selective formation of gap junction channels in connexin-transfected HeLa cells. J Cell Biol 1995, 129:805-817.
8. Elstrott J., Anishchenko A., Greschner M., Sher A., Litke A.M., Chichilnisky E.J., Feller M.B. Direction selectivity in the retina is established independent of visual experience and cholinergic retinal waves. Neuron 2008, 58:499-506.
9. Famiglietti E.V. Dendritic co-stratification of ON and ON-OFF directionally selective ganglion cells with starburst amacrine cells in rabbit retina. J Comp Neurol 1992, 324:322-335.
10. Fried S.I., Munch T.A., Werblin F.S. Mechanisms and circuitry underlying directional selectivity in the retina. Nature 2002, 420:411-414.
11. Gong S., Zheng C., Doughty M.L., Losos K., Didkovsky N., Schambra U.B., Nowak N.J., Joyner A., Leblanc G., Hatten M.E., Heintz N. A gene expression atlas of the central nervous system based on bacterial artificial chromosomes. Nature 2003, 425:917-925.
12. He S., Masland R.H. ON direction-selective ganglion cells in the rabbit retina: dendritic morphology and pattern of fasciculation. Vis Neurosci 1998, 15:369-375.
13. Huberman A.D., Wei W., Elstrott J., Stafford B.K., Feller M.B., Barres B.A. Genetic identification of an ON-OFF direction-selective retinal ganglion cell subtype reveals a layer-specific subcortical map of posterior motion. Neuron 2009, 62:327-334.
14. Kanjhan R., Vaney D.I. Semi-loose seal neurobiotin electroporation for combined structural and functional analysis of neurons. Pflugers Arch 2008, 457:561-568.
15. Kay J.N., De la Huerta I., Kim I.J., Zhang Y., Yamagata M., Chu M.W., Meister M., Sanes J.R. Retinal ganglion cells with distinct directional preferences differ in molecular identity, structure, and central projections. J Neurosci 2011, 31:7753-7762.
16. Kim I.J., Zhang Y., Yamagata M., Meister M., Sanes J.R. Molecular identification of a retinal cell type that responds to upward motion. Nature 2008, 452:478-482.
17. Lee S., Kim K., Zhou Z.J. Role of ACh-GABA cotransmission in detecting image motion and motion direction. Neuron 2010, 68:1159-1172.
18. Oyster C.W. The analysis of image motion by the rabbit retina. J Physiol 1968, 199:613-635.
19. Pan F., Paul D.L., Bloomfield S.A., Volgyi B. Connexin36 is required for gap junctional coupling of most ganglion cell subtypes in the mouse retina. J Comp Neurol 2010, 518:911-927.
20. Paul D., Ebihara L., Takemoto L., Swenson K., Goodenough D. Connexin46, a novel lens gap junction protein, induces voltage-gated currents in nonjunctional plasma membrane of xenopus oocytes. J Cell Biol 1991, 115:1077-1089.
21. Perez D.E.S.M.L., Dedek K., Janssen-Bienhold U., Meyer A., Kreuzberg M.M., Lorenz S., Willecke K., Weiler R. Expression and modulation of connexin30.2, a novel gap junction protein in the mouse retina. Vis Neurosci 2010, 27:91-101.
22. Schubert T., Degen J., Willecke K., Hormuzdi S.G., Monyer H., Weiler R. Connexin36 mediates gap junctional coupling of alpha-ganglion cells in mouse retina. J Comp Neurol 2005, 485:191-201.
23. Schubert T., Maxeiner S., Kruger O., Willecke K., Weiler R. Connexin45 mediates gap junctional coupling of bistratified ganglion cells in the mouse retina. J Comp Neurol 2005, 490:29-39.
24. Sun W., Li N., He S. Large-scale morphological survey of mouse retinal ganglion cells. J Comp Neurol 2002, 451:115-126.
25. Sun W., Deng Q., Levick W.R., He S. ON direction-selective ganglion cells in the mouse retina. J Physiol 2006, 576:197-202.
26. Trenholm S., Johnson K., Li X., Smith Robert G., Awatramani Gautam B. Parallel mechanisms encode direction in the retina. Neuron 2013, 77:204-208.
27. Vaney D.I. Many diverse types of retinal neurons show tracer coupling when injected with biocytin or neurobiotin. Neurosci Lett 1991, 125:187-190.
28. Vaney D.I. Territorial organization of direction-selective ganglion cells in rabbit retina. J Neurosci 1994, 14:6301-6316.
29. Vaney D.I., Pow D.V. The dendritic architecture of the cholinergic plexus in the rabbit retina: selective labeling by glycine accumulation in the presence of sarcosine. J Comp Neurol 2000, 421:1-13.
30. Volgyi B., Chheda S., Bloomfield S.A. Tracer coupling patterns of the ganglion cell subtypes in the mouse retina. J Comp Neurol 2009, 512:664-687.
31. Wei W., Hamby A.M., Zhou K., Feller M.B. Development of asymmetric inhibition underlying direction selectivity in the retina. Nature 2011, 469:402-406.
32. Weng S., Sun W., He S. Identification of ON-OFF direction-selective ganglion cells in the mouse retina. J Physiol 2005, 562:915-923.
33. Yang G., Masland R.H. Direct visualization of the dendritic and receptive fields of directionally selective retinal ganglion cells. Science 1992, 258:1949-1952.
34. Yang G., Masland R.H. Receptive fields and dendritic structure of directionally selective retinal ganglion cells. J Neurosci 1994, 14:5267-5280.
35. Yonehara K., Shintani T., Suzuki R., Sakuta H., Takeuchi Y., Nakamura-Yonehara K., Noda M. Expression of SPIG1 reveals development of a retinal ganglion cell subtype projecting to the medial terminal nucleus in the mouse. PLoS One 2008, 3:e1533.
36. Yonehara K., Ishikane H., Sakuta H., Shintani T., Nakamura-Yonehara K., Kamiji N.L., Usui S., Noda M. Identification of retinal ganglion cells and their projections involved in central transmission of information about upward and downward image motion. PLoS One 2009, 4:e4320.
37. Yonehara K., Balint K., Noda M., Nagel G., Bamberg E., Roska B. Spatially asymmetric reorganization of inhibition establishes a motion-sensitive circuit. Nature 2011, 469:407-410.