Department of Biochemistry and Molecular Biology, Hotchkiss Brain Institute, Alberta Children's Hospital Research Institute, University of Calgary, Calgary, Alberta, Canada.
PLoS One. 2012;7(3):e32795. doi: 10.1371/journal.pone.0032795. Epub 2012 Mar 5.
The retina has a unique three-dimensional architecture, the precise organization of which allows for complete sampling of the visual field. Along the radial or apicobasal axis, retinal neurons and their dendritic and axonal arbors are segregated into layers, while perpendicular to this axis, in the tangential plane, four of the six neuronal types form patterned cellular arrays, or mosaics. Currently, the molecular cues that control retinal cell positioning are not well-understood, especially those that operate in the tangential plane. Here we investigated the role of the PTEN phosphatase in establishing a functional retinal architecture.
METHODOLOGY/PRINCIPAL FINDINGS: In the developing retina, PTEN was localized preferentially to ganglion, amacrine and horizontal cells, whose somata are distributed in mosaic patterns in the tangential plane. Generation of a retina-specific Pten knock-out resulted in retinal ganglion, amacrine and horizontal cell hypertrophy, and expansion of the inner plexiform layer. The spacing of Pten mutant mosaic populations was also aberrant, as were the arborization and fasciculation patterns of their processes, displaying cell type-specific defects in the radial and tangential dimensions. Irregular oscillatory potentials were also observed in Pten mutant electroretinograms, indicative of asynchronous amacrine cell firing. Furthermore, while Pten mutant RGC axons targeted appropriate brain regions, optokinetic spatial acuity was reduced in Pten mutant animals. Finally, while some features of the Pten mutant retina appeared similar to those reported in Dscam-mutant mice, PTEN expression and activity were normal in the absence of Dscam.
CONCLUSIONS/SIGNIFICANCE: We conclude that Pten regulates somal positioning and neurite arborization patterns of a subset of retinal cells that form mosaics, likely functioning independently of Dscam, at least during the embryonic period. Our findings thus reveal an unexpected level of cellular specificity for the multi-purpose phosphatase, and identify Pten as an integral component of a novel cell positioning pathway in the retina.
视网膜具有独特的三维结构,其精确的组织允许对整个视野进行完全采样。沿着径向或顶底轴,视网膜神经元及其树突和轴突树突被分隔成层,而垂直于这个轴,在切平面中,六种神经元类型中的四种形成有图案的细胞阵列,或镶嵌物。目前,控制视网膜细胞定位的分子线索还不是很清楚,特别是那些在切平面中起作用的线索。在这里,我们研究了 PTEN 磷酸酶在建立功能性视网膜结构中的作用。
方法/主要发现:在发育中的视网膜中,PTEN 优先定位于神经节细胞、无长突细胞和水平细胞,其体位于切平面中呈镶嵌模式分布。生成视网膜特异性 Pten 敲除导致视网膜神经节细胞、无长突细胞和水平细胞肥大,并扩大了内丛状层。Pten 突变体镶嵌群体的间隔也异常,其过程的分支和聚集模式也异常,表现出径向和切向维度的细胞类型特异性缺陷。Pten 突变体视网膜电图中也观察到不规则的振荡电位,表明无长突细胞的发射不同步。此外,虽然 Pten 突变体 RGC 轴突靶向适当的大脑区域,但 Pten 突变体动物的光动空间锐度降低。最后,虽然 Pten 突变体视网膜的一些特征与 Dscam 突变体小鼠报告的特征相似,但在没有 Dscam 的情况下,PTEN 的表达和活性是正常的。
结论/意义:我们得出结论,Pten 调节形成镶嵌物的一部分视网膜细胞的体定位和神经突分支模式,可能在胚胎期至少独立于 Dscam 发挥作用。我们的研究结果因此揭示了多用途磷酸酶对细胞特异性的意外水平,并确定 Pten 是视网膜中一种新的细胞定位途径的组成部分。