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Morphology of dopaminergic amacrine cells in the mouse retina: Independence from homotypic interactions

✍ Scribed by Patrick W. Keeley; Benjamin E. Reese


Publisher
John Wiley and Sons
Year
2009
Tongue
English
Weight
713 KB
Volume
518
Category
Article
ISSN
0021-9967

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✦ Synopsis


Abstract

To determine the role of homotypic interactions between neighboring dopaminergic amacrine (DA) cells upon dendritic morphogenesis, the morphology of single cells was examined relative to the positioning of all neighboring homotypic cells. For each labeled cell, the dendritic field was reconstructed, its Voronoi domain was calculated, and the two were related. The dendritic fields of DA cells were observed to be large, sparse, and highly irregular. Dendrites readily overlapped those of neighboring cells, showing no evidence for dendritic tiling or inter‐digitation consistent with homotypic repulsion or avoidance. Furthermore, a direct comparison of dendritic field area with the Voronoi domain area of the same cell showed no evidence for dendritic growth being constrained or biased by the local distribution of homotypic neighbors in wild‐type retinas. A comparison of the processes of adjacent filled cells confirmed their immediate proximity to one another within the inner plexiform layer, indicating that they do not engage in mutual avoidance by coursing at different depths. Together, these results suggest that the morphogenesis of DA cells is independent of homotypic interactions. However, in the absence of the pro‐apoptotic Bax gene, which yields a fourfold increase in DA cell number, a small but significant reduction in dendritic field size was obtained, although not so great as would be predicted by the increase in density. The present results are considered in light of recent studies on the role of cell adhesion molecules expressed by developing DA cells. J. Comp. Neurol. 518:1220–1231, 2010. Β© 2009 Wiley‐Liss, Inc.


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The authors wish to point out an error in Figure 10 of this paper. Dendrites in this schematic drawing are shown in red and axons are shown in green, not the reverse as indicated in the key to the originally published version. A corrected figure and the correct legend for this figure are shown below