John F. Hardesty, MD, Department of Ophthalmology and Visual Sciences, Washington University School of Medicine, St. Louis, Missouri 63110
John F. Hardesty, MD, Department of Ophthalmology and Visual Sciences, Washington University School of Medicine, St. Louis, Missouri 63110.
J Neurosci. 2022 Mar 30;42(13):2678-2689. doi: 10.1523/JNEUROSCI.1164-21.2022. Epub 2022 Feb 15.
Dendrite and axon arbor sizes are critical to neuronal function and vary widely between different neuron types. The relative dendrite and axon sizes of synaptic partners control signal convergence and divergence in neural circuits. The developmental mechanisms that determine cell-type-specific dendrite and axon size and match synaptic partners' arbor territories remain obscure. Here, we discover that retinal horizontal cells express the leucine-rich repeat domain cell adhesion molecule AMIGO1. Horizontal cells provide pathway-specific feedback to photoreceptors-horizontal cell axons to rods and horizontal cell dendrites to cones. AMIGO1 selectively expands the size of horizontal cell axons. When is deleted in all or individual horizontal cells of either sex, their axon arbors shrink. By contrast, horizontal cell dendrites and synapse formation of horizontal cell axons and dendrites are unaffected by AMIGO1 removal. The dendrites of rod bipolar cells, which do not express AMIGO1, shrink in parallel with horizontal cell axons in () mice. This territory matching maintains the function of the rod bipolar pathway, preserving bipolar cell responses and retinal output signals in mice. We previously identified AMIGO2 as a scaling factor that constrains retinal neurite arbors. Our current results identify AMIGO1 as a scaling factor that expands retinal neurite arbors and reveal territory matching as a novel homeostatic mechanism. Territory matching interacts with other homeostatic mechanisms to stabilize the development of the rod bipolar pathway, which mediates vision near the threshold. Neurons send and receive signals through branched axonal and dendritic arbors. The size of these arbors is critical to the function of a neuron. Axons and dendrites grow during development and are stable at maturity. The mechanisms that determine axon and dendrite size are not well understood. Here, we identify a cell surface protein, AMIGO1, that selectively promotes axon growth of horizontal cells, a retinal interneuron. Removal of AMIGO1 reduces the size of horizontal cell axons without affecting the size of their dendrites or the ability of both arbors to form connections. The changes in horizontal cell axons are matched by changes in synaptic partner dendrites to stabilize retinal function. This identifies territory matching as a novel homeostatic plasticity mechanism.
树突和轴突分支的大小对神经元的功能至关重要,不同神经元类型之间的差异很大。突触前神经元和后神经元相对的树突和轴突大小控制着神经回路中信号的汇聚和发散。决定特定细胞类型的树突和轴突大小并匹配突触前神经元树突领域的发育机制仍不清楚。在这里,我们发现视网膜水平细胞表达富含亮氨酸重复的细胞粘附分子 AMIGO1。水平细胞为光感受器-水平细胞轴突提供了特定途径的反馈,为水平细胞树突和视锥细胞提供了反馈。AMIGO1 选择性地扩大了水平细胞轴突的大小。当雄性或雌性所有或个别水平细胞中的 缺失时,它们的轴突分支缩小。相比之下,水平细胞的树突以及水平细胞轴突和树突的突触形成不受 AMIGO1 缺失的影响。不表达 AMIGO1 的视杆双极细胞的树突与 ()小鼠中的水平细胞轴突平行缩小。这种领域匹配维持了视杆双极通路的功能,在 小鼠中保留了双极细胞的反应和视网膜输出信号。我们之前将 AMIGO2 鉴定为限制视网膜神经突分支的缩放因子。我们当前的结果确定 AMIGO1 为扩展视网膜神经突分支的缩放因子,并揭示了领域匹配作为一种新的平衡机制。领域匹配与其他平衡机制相互作用,以稳定介导阈值附近视觉的视杆双极通路的发育。神经元通过分支的轴突和树突分支发送和接收信号。这些分支的大小对神经元的功能至关重要。轴突和树突在发育过程中生长,并在成熟时保持稳定。决定轴突和树突大小的机制尚不清楚。在这里,我们鉴定了一种细胞表面蛋白 AMIGO1,它选择性地促进了视网膜中间神经元水平细胞的轴突生长。AMIGO1 的缺失减少了水平细胞轴突的大小,而不影响其树突的大小或两者分支形成连接的能力。水平细胞轴突的变化与突触后神经元树突的变化相匹配,以稳定视网膜的功能。这将领域匹配确定为一种新的平衡可塑性机制。