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Cell numbers, cell ratios, and developmental plasticity in the rod pathway of the mouse retina

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JOURNAL OF ANATOMY
卷 243, 期 2, 页码 204-222

出版社

WILEY
DOI: 10.1111/joa.13653

关键词

amacrine cell; Bax; coverage factor; recombinant inbred strain; rod bipolar cell; rod photoreceptor

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The precise specification of cellular fate is important for the production of the correct number of neurons. Cell death may control cell number and refine the ratio of pre- to post-synaptic neurons. This study explores the size and variability of different neuronal populations in the mouse retina, as well as the plasticity involved in establishing connectivity between these populations.
The precise specification of cellular fate is thought to ensure the production of the correct number of neurons within a population. Programmed cell death may be an additional mechanism controlling cell number, believed to refine the proper ratio of pre- to post-synaptic neurons for a given species. Here, we consider the size of three different neuronal populations in the rod pathway of the mouse retina: rod photoreceptors, rod bipolar cells, and AII amacrine cells. Across a collection of 28 different strains of mice, large variation in the numbers of all three cell types is present. The variation in their numbers is not correlated, so that the ratio of rods to rod bipolar cells, as well as rod bipolar cells to AII amacrine cells, varies as well. Establishing connectivity between such variable pre- and post-synaptic populations relies upon plasticity that modulates process outgrowth and morphological differentiation, which we explore experimentally for both rod bipolar and AII amacrine cells in a mouse retina with elevated numbers of each cell type. While both rod bipolar dendritic and axonal arbors, along with AII lobular arbors, modulate their areal size in relation to local homotypic cell densities, the dendritic appendages of the AII amacrine cells do not. Rather, these processes exhibit a different form of plasticity, regulating the branching density of their overlapping arbors. Each form of plasticity should ensure uniformity in retinal coverage in the presence of the independent specification of afferent and target cell number.

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