首页> 外文期刊>Visual Neuroscience: An International Journal for Empirical and Theoretical Research >Developmental improvement in the regularity and packing of mouse horizontal cells: implications for mechanisms underlying mosaic pattern formation.
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Developmental improvement in the regularity and packing of mouse horizontal cells: implications for mechanisms underlying mosaic pattern formation.

机译:小鼠水平细胞的规则性和堆积发育改进:对镶嵌图案形成机制的影响。

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The present investigation has sought to determine whether the population of retinal horizontal cells undergoes an increase in the precision of its mosaic patterning during postnatal development, and if so, whether this increase is compatible with three different mechanistic accounts of retinal mosaic formation. Horizontal cells were labeled with antibodies to neurofilaments or calbindin at different developmental stages, and then visualized in retinal wholemounts. Multiple fields were sampled from each retina to determine horizontal cell density, while the X-Y coordinates of each cell in a field were determined. An estimate of total horizontal cell number was calculated for each retina, while the Voronoi domain regularity index and the packing factor were computed for each field. Two strains of mice showing a two-fold difference in the size of their horizontal cell population in maturity were sampled, C57BL/6J and A/J. Horizontal cell number in C57BL/6J was approximately twice that observed in A/J at all postnatal stages, with neither strain showing an effect of age on horizontal cell number. In both strains, however, the Voronoi domain regularity index and the packing factor were significantly lower at P-1 relative to later developmental stages. These results show that accounts of mosaic formation proposing the selective death of irregularly positioned cells, or the periodic occurrence of fate-determining events, are insufficient to establish the final patterning achieved by horizontal cells. Rather, they support the hypothesis that tangential dispersion enhances mosaic patterning during postnatal development.
机译:本研究试图确定视网膜水平细胞的种群在出生后发育期间是否经历了镶嵌图案精度的提高,如果是,这种增加是否与视网膜镶嵌形成的三种不同机制相吻合。用在不同发育阶段的神经丝或钙结合蛋白抗体标记水平细胞,然后在视网膜全壁镜中观察。从每个视网膜采样多个视野以确定水平细胞密度,同时确定视野中每个细胞的X-Y坐标。计算每个视网膜的水平细胞总数,同时计算每个视野的Voronoi域规则指数和堆积因子。抽取了两只小鼠,它们的水平细胞群体在成熟度上显示出两倍的差异,分别是C57BL / 6J和A / J。在所有出生后阶段,C57BL / 6J中的水平细胞数量约为A / J中观察到的水平细胞数量的两倍,两种菌株均未显示出年龄对水平细胞数量的影响。然而,在这两个菌株中,相对于后期的发育阶段,P-1的Voronoi域规则性指数和堆积因子均显着较低。这些结果表明,镶嵌形成的结果提出了定位不规则的细胞的选择性死亡或命运决定事件的周期性发生,不足以建立水平细胞实现的最终图案。相反,他们支持这样的假设,即切线散布会在出生后的发育过程中增强镶嵌图案。

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