Department of Neuroscience and Department of Cell Biology, Yale University School of Medicine, New Haven, United States.
Laboratory of High Resolution Optical Imaging, National Institute of Biomedical Imaging and Bioengineering, National Institutes of Health, Bethesda, United States.
Elife. 2021 Nov 16;10:e71171. doi: 10.7554/eLife.71171.
During development, neurites and synapses segregate into specific neighborhoods or layers within nerve bundles. The developmental programs guiding placement of neurites in specific layers, and hence their incorporation into specific circuits, are not well understood. We implement novel imaging methods and quantitative models to document the embryonic development of the brain neuropil and discover that differential adhesion mechanisms control precise placement of single neurites onto specific layers. Differential adhesion is orchestrated via developmentally regulated expression of the IgCAM SYG-1, and its partner ligand SYG-2. Changes in SYG-1 expression across neuropil layers result in changes in adhesive forces, which sort SYG-2-expressing neurons. Sorting to layers occurs, not via outgrowth from the neurite tip, but via an alternate mechanism of retrograde zippering, involving interactions between neurite shafts. Our study indicates that biophysical principles from differential adhesion govern neurite placement and synaptic specificity in vivo in developing neuropil bundles.
在发育过程中,神经突和突触会分离到神经束内的特定区域或层。指导神经突在特定层中定位的发育程序,以及它们被整合到特定回路中的程序,目前还不太清楚。我们采用新的成像方法和定量模型来记录脑神经丛的胚胎发育,发现差异粘附机制控制着单个神经突精确地定位于特定的层。差异粘附通过发育调节表达的 IgCAM SYG-1 及其配体 SYG-2 来协调。SYG-1 在神经丛层中的表达变化导致粘附力的变化,从而对 SYG-2 表达的神经元进行分类。排序到层发生,不是通过神经突尖端的生长,而是通过涉及神经突轴之间相互作用的逆行拉链的替代机制。我们的研究表明,从差异粘附中得出的生物物理原理控制着体内发育中的神经丛束中神经突的放置和突触的特异性。