Transient neurites of retinal horizontal cells exhibit columnar tiling via homotypic interactions (original) (raw)

References

  1. Gan, W.B. & Macagno, E.R. Interactions between segmental homologs and between isoneuronal branches guide the formation of sensory terminal fields. J. Neurosci. 15, 3243–3253 (1995).
    Article CAS Google Scholar
  2. Grueber, W.B., Ye, B., Moore, A.W., Jan, L.Y. & Jan, Y.N. Dendrites of distinct classes of Drosophila sensory neurons show different capacities for homotypic repulsion. Curr. Biol. 13, 618–626 (2003).
    Article CAS Google Scholar
  3. Sugimura, K. et al. Distinct developmental modes and lesion-induced reactions of dendrites of two classes of Drosophila sensory neurons. J. Neurosci. 23, 3752–3760 (2003).
    Article CAS Google Scholar
  4. Wassle, H., Peichl, L. & Boycott, B.B. Mosaics and territories of cat retinal ganglion cells. Prog. Brain Res. 58, 183–190 (1983).
    Article CAS Google Scholar
  5. Vaney, D.I. The mosaic of amacrine cells in the mammalian retina. Prog. Retin. Res. 9, 49–100 (1990).
    Article CAS Google Scholar
  6. Raven, M.A., Stagg, S.B., Nassar, H. & Reese, B.E. Developmental improvement in the regularity and packing of mouse horizontal cells: implications for mechanisms underlying mosaic pattern formation. Vis. Neurosci. 22, 569–573 (2005).
    Article Google Scholar
  7. Hinds, J.W. & Hinds, P.L. Differentiation of photoreceptors and horizontal cells in the embryonic mouse retina: an electron microscopic, serial section analysis. J. Comp. Neurol. 187, 495–511 (1979).
    Article CAS Google Scholar
  8. Schnitzer, J. & Rusoff, A.C. Horizontal cells of the mouse retina contain glutamic acid decarboxylase–like immunoreactivity during early developmental stages. J. Neurosci. 4, 2948–2955 (1984).
    Article CAS Google Scholar
  9. Poche, R.A. et al. Somal positioning and dendritic growth of horizontal cells are regulated by interactions with homotypic neighbors. Eur. J. Neurosci. 27, 1607–1614 (2008).
    Article Google Scholar
  10. Rossi, C., Strettoi, E. & Galli-Resta, L. The spatial order of horizontal cells is not affected by massive alterations in the organization of other retinal cells. J. Neurosci. 23, 9924–9928 (2003).
    Article CAS Google Scholar
  11. Chattopadhyaya, B. et al. Experience and activity-dependent maturation of perisomatic GABAergic innervation in primary visual cortex during a postnatal critical period. J. Neurosci. 24, 9598–9611 (2004).
    Article CAS Google Scholar
  12. Peichl, L. & Gonzalez-Soriano, J. Morphological types of horizontal cell in rodent retinae: a comparison of rat, mouse, gerbil and guinea pig. Vis. Neurosci. 11, 501–517 (1994).
    Article CAS Google Scholar
  13. Haverkamp, S. & Wassle, H. Immunocytochemical analysis of the mouse retina. J. Comp. Neurol. 424, 1–23 (2000).
    Article CAS Google Scholar
  14. Ramón y Cajal, S. Studies on vertebrate neurogenesis (Thomas, Springfield, Illinois, 1960).
    Google Scholar
  15. Reese, B.E., Raven, M.A. & Stagg, S.B. Afferents and homotypic neighbors regulate horizontal cell morphology, connectivity and retinal coverage. J. Neurosci. 25, 2167–2175 (2005).
    Article CAS Google Scholar
  16. Edqvist, P.H. & Hallbook, F. Newborn horizontal cells migrate bi-directionally across the neuroepithelium during retinal development. Development 131, 1343–1351 (2004).
    Article CAS Google Scholar
  17. Reese, B.E., Harvey, A.R. & Tan, S.S. Radial and tangential dispersion patterns in the mouse retina are cell-class specific. Proc. Natl. Acad. Sci. USA 92, 2494–2498 (1995).
    Article CAS Google Scholar
  18. Reese, B.E., Necessary, B.D., Tam, P.P., Faulkner-Jones, B. & Tan, S.S. Clonal expansion and cell dispersion in the developing mouse retina. Eur. J. Neurosci. 11, 2965–2978 (1999).
    Article CAS Google Scholar
  19. Rodieck, R.W. The density recovery profile: a method for the analysis of points in the plane applicable to retinal studies. Vis. Neurosci. 6, 95–111 (1991).
    Article CAS Google Scholar
  20. Blanks, J.C., Adinolfi, A.M. & Lolley, R.N. Synaptogenesis in the photoreceptor terminal of the mouse retina. J. Comp. Neurol. 156, 81–93 (1974).
    Article CAS Google Scholar
  21. Young, R.W. Cell proliferation during postnatal development of the retina in the mouse. Brain Res. 353, 229–239 (1985).
    Article CAS Google Scholar
  22. Rich, K.A., Zhan, Y. & Blanks, J.C. Migration and synaptogenesis of cone photoreceptors in the developing mouse retina. J. Comp. Neurol. 388, 47–63 (1997).
    Article CAS Google Scholar
  23. Sherry, D.M., Wang, M.M., Bates, J. & Frishman, L.J. Expression of vesicular glutamate transporter 1 in the mouse retina reveals temporal ordering in development of rod vs. cone and ON vs. OFF circuits. J. Comp. Neurol. 465, 480–498 (2003).
    Article CAS Google Scholar
  24. Sharma, R.K., O'Leary, T.E., Fields, C.M. & Johnson, D.A. Development of the outer retina in the mouse. Brain Res. Dev. Brain Res. 145, 93–105 (2003).
    Article CAS Google Scholar
  25. Godinho, L. et al. Nonapical symmetric divisions underlie horizontal cell layer formation in the developing retina in vivo. Neuron 56, 597–603 (2007).
    Article CAS Google Scholar
  26. Godinho, L. et al. Targeting of amacrine cell neurites to appropriate synaptic laminae in the developing zebrafish retina. Development 132, 5069–5079 (2005).
    Article CAS Google Scholar
  27. Nadarajah, B., Alifragis, P., Wong, R.O. & Parnavelas, J.G. Neuronal migration in the developing cerebral cortex: observations based on real-time imaging. Cereb. Cortex 13, 607–611 (2003).
    Article CAS Google Scholar
  28. Solecki, D.J., Model, L., Gaetz, J., Kapoor, T.M. & Hatten, M.E. Par6alpha signaling controls glial-guided neuronal migration. Nat. Neurosci. 7, 1195–1203 (2004).
    Article CAS Google Scholar
  29. Bellion, A., Baudoin, J.P., Alvarez, C., Bornens, M. & Metin, C. Nucleokinesis in tangentially migrating neurons comprises two alternating phases: forward migration of the Golgi/centrosome associated with centrosome splitting and myosin contraction at the rear. J. Neurosci. 25, 5691–5699 (2005).
    Article CAS Google Scholar
  30. Schaar, B.T. & McConnell, S.K. Cytoskeletal coordination during neuronal migration. Proc. Natl. Acad. Sci. USA 102, 13652–13657 (2005).
    Article CAS Google Scholar
  31. Eglen, S.J., van Ooyen, A. & Willshaw, D.J. Lateral cell movement driven by dendritic interactions is sufficient to form retinal mosaics. Network 11, 103–118 (2000).
    Article CAS Google Scholar
  32. Lin, B., Wang, S.W. & Masland, R.H. Retinal ganglion cell type, size and spacing can be specified independent of homotypic dendritic contacts. Neuron 43, 475–485 (2004).
    Article CAS Google Scholar
  33. Farajian, R., Raven, M.A., Cusato, K. & Reese, B.E. Cellular positioning and dendritic field size of cholinergic amacrine cells are impervious to early ablation of neighboring cells in the mouse retina. Vis. Neurosci. 21, 13–22 (2004).
    Article Google Scholar
  34. Raven, M.A., Oh, E.C., Swaroop, A. & Reese, B.E. Afferent control of horizontal cell morphology revealed by genetic respecification of rods and cones. J. Neurosci. 27, 3540–3547 (2007).
    Article CAS Google Scholar
  35. Jeyarasasingam, G., Snider, C.J., Ratto, G.M. & Chalupa, L.M. Activity-regulated cell death contributes to the formation of ON and OFF alpha ganglion cell mosaics. J. Comp. Neurol. 394, 335–343 (1998).
    Article CAS Google Scholar
  36. Galli-Resta, L., Novelli, E. & Viegi, A. Dynamic microtubule-dependent interactions position homotypic neurones in regular monolayered arrays during retinal development. Development 129, 3803–3814 (2002).
    CAS PubMed Google Scholar
  37. Novelli, E., Leone, P., Resta, V. & Galli-Resta, L. A three-dimensional analysis of the development of the horizontal cell mosaic in the rat retina: implications for the mechanisms controlling pattern formation. Vis. Neurosci. 24, 91–98 (2007).
    Article Google Scholar
  38. Tyler, M.J., Carney, L.H. & Cameron, D.A. Control of cellular pattern formation in the vertebrate inner retina by homotypic regulation of cell-fate decisions. J. Neurosci. 25, 4565–4576 (2005).
    Article CAS Google Scholar
  39. McCabe, K.L., Gunther, E.C. & Reh, T.A. The development of the pattern of retinal ganglion cells in the chick retina: mechanisms that control differentiation. Development 126, 5713–5724 (1999).
    CAS PubMed Google Scholar
  40. Perry, V.H. & Linden, R. Evidence for dendritic competition in the developing retina. Nature 297, 683–685 (1982).
    Article CAS Google Scholar
  41. Hitchcock, P.F. Exclusionary dendritic interactions in the retina of the goldfish. Development 106, 589–598 (1989).
    CAS PubMed Google Scholar
  42. Sagasti, A., Guido, M.R., Raible, D.W. & Schier, A.F. Repulsive interactions shape the morphologies and functional arrangement of zebrafish peripheral sensory arbors. Curr. Biol. 15, 804–814 (2005).
    Article CAS Google Scholar
  43. Stacy, R.C. & Wong, R.O. Developmental relationship between cholinergic amacrine cell processes and ganglion cell dendrites of the mouse retina. J. Comp. Neurol. 456, 154–166 (2003).
    Article Google Scholar
  44. Shelley, J. et al. Horizontal cell receptive fields are reduced in connexin57-deficient mice. Eur. J. Neurosci. 23, 3176–3186 (2006).
    Article Google Scholar
  45. Roberts, M.R., Srinivas, M., Forrest, D., Morreale de Escobar, G. & Reh, T.A. Making the gradient: thyroid hormone regulates cone opsin expression in the developing mouse retina. Proc. Natl. Acad. Sci. USA 103, 6218–6223 (2006).
    Article CAS Google Scholar
  46. Morgan, J.L., Schubert, T. & Wong, R.O. Developmental patterning of glutamatergic synapses onto retinal ganglion cells. Neural Develop. 3, 8 (2008).
    Article Google Scholar

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