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Deterministic fate assignment of Müller glia cells in the zebrafish retina suggests a clonal backbone during development

机译:斑马鱼视网膜中Müller胶质细胞的确定性命运分配表明发育过程中存在克隆主链

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摘要

The optic cup houses multipotent retinal progenitor cells that proliferate and differentiate to form the mature retina, containing five main types of neurons and a single glial cell type, the Müller cell. Progenitors of the zebrafish optic cup generate clones that vary regarding the number and types of neurons, a process we previously showed could be described by stochastic models. Here, we present data indicating that each retinal progenitor cell, in the 24 hrs post‐fertilization optic cup, is predestined to form a single Müller cell. This striking fate assignment of Müller cells reveals a dual nature of retinal lineages where stochastic mechanisms produce variable numbers of neurons while there is a strong deterministic component governing the formation of glia cells. A possible mechanism for this stereotypic fate assignment could be the maintenance of a clonal backbone during retina development, which would be similar to invertebrate and rodent cortical neurogenesis.
机译:视杯装有多能性视网膜祖细胞,它们增殖并分化形成成熟的视网膜,其中包含五种主要类型的神经元和一种神经胶质细胞类型(Müller细胞)。斑马鱼视杯的祖细胞产生的克隆在神经元的数量和类型方面各不相同,我们先前展示的过程可以用随机模型描述。在这里,我们提供的数据表明,受精后视杯中的每个视网膜祖细胞都注定会形成单个Müller细胞。 Müller细胞的这种惊人的命运分配揭示了视网膜谱系的双重性质,其中随机机制产生可变数量的神经元,同时有很强的决定性成分控制神经胶质细胞的形成。这种刻板的命运分配的可能机制可能是在视网膜发育过程中维持克隆主干,这类似于无脊椎动物和啮齿动物的皮质神经发生。

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