Keeley Patrick W, Whitney Irene E, Madsen Nils R, St John Ace J, Borhanian Sarra, Leong Stephanie A, Williams Robert W, Reese Benjamin E
Neuroscience Research Institute, University of California, Santa Barbara, Santa Barbara, CA 93106, USA; Department of Molecular, Cellular, and Developmental Biology, University of California, Santa Barbara, Santa Barbara, CA 93106, USA.
Neuroscience Research Institute, University of California, Santa Barbara, Santa Barbara, CA 93106, USA.
Dev Cell. 2014 Jul 14;30(1):103-9. doi: 10.1016/j.devcel.2014.05.003. Epub 2014 Jun 19.
The sizes of different neuronal populations within the CNS are precisely controlled, but whether neuronal number is coordinated between cell types is unknown. We examined the covariance structure of 12 different retinal cell types across 30 genetically distinct lines of mice, finding minimal covariation when comparing synaptically connected or developmentally related cell types. Variation mapped to one or more genomic loci for each cell type, but rarely were these shared, indicating minimal genetic coregulation of final number. Multiple genes, therefore, participate in the specification of the size of every population of retinal neuron, yet genetic variants work largely independent of one another during development to modulate those numbers, yielding substantial variability in the convergence ratios between pre- and postsynaptic populations. Density-dependent cellular interactions in the outer plexiform layer overcome this variability to ensure the formation of neuronal circuits that maintain constant retinal coverage and complete afferent sampling.
中枢神经系统内不同神经元群体的大小受到精确控制,但尚不清楚细胞类型之间的神经元数量是否协调。我们研究了30个基因不同品系小鼠中12种不同视网膜细胞类型的协方差结构,发现比较突触连接或发育相关的细胞类型时,协方差极小。每种细胞类型的变异映射到一个或多个基因组位点,但这些位点很少共享,这表明最终数量的遗传共调控作用极小。因此,多个基因参与了每个视网膜神经元群体大小的确定,但在发育过程中,基因变异在很大程度上彼此独立起作用来调节这些数量,导致突触前和突触后群体之间的汇聚比率存在很大差异。外网状层中密度依赖性细胞相互作用克服了这种变异性,以确保形成维持恒定视网膜覆盖和完整传入采样的神经元回路。