Laboratory of Neuroscience, Graduate School of Pharmaceutical Sciences, Hokkaido University, Sapporo 060-0812, Japan.
Exploratory Research Center on Life and Living Systems (ExCELLS), Okazaki, Aichi 444-8787, Japan.
Mol Biol Cell. 2023 Oct 1;34(11):ar110. doi: 10.1091/mbc.E22-10-0495. Epub 2023 Aug 16.
Alcadein α (Alcα) and amyloid-β protein precursor (APP) are cargo receptors that associate vesicles with kinesin-1. These vesicles, which contain either Alcα or APP, transport various proteins/cargo molecules into axon nerve terminals. Here, we analyzed immune-isolated Alcα- and APP-containing vesicles of adult mouse brains with LC-MS/MS and identified proteins present in vesicles that contained either Alcα or APP. Among these proteins, Frizzled-5 (Fzd5), a Wnt receptor, was detected mainly in Alcα vesicles. Although colocalization ratios of Fzd5 with Alcα are low in the neurites of differentiating neurons by a low expression of Fzd5 in embryonic brains, the suppression of Alcα expression decreased the localization of Fzd5 in neurites of primary cultured neurons. Furthermore, Fzd5-EGFP expressed in primary cultured neurons was preferentially transported in axons with the transport velocities of Alcα vesicles. In synaptosomal fractions of adult-mice brains that express higher levels of Fzd5, the amount of Fzd5 and the phosphorylation level of calcium/calmodulin-dependent protein kinase-II were reduced in the Alcα-deficient mice. These results suggest that reduced transport of Fzd5 by Alcα-containing vesicles associated with kinesin-1 in axon terminals may impair the response to Wnt ligands in the noncanonical Ca-dependent signal transduction pathway at nerve terminals of mature neurons.
Alcadein α (Alcα) 和淀粉样前体蛋白 (APP) 是货物受体,它们将囊泡与驱动蛋白-1 结合。这些含有 Alcα 或 APP 的囊泡将各种蛋白质/货物分子运输到轴突神经末梢。在这里,我们通过 LC-MS/MS 分析了成年小鼠大脑中免疫分离的含有 Alcα 和 APP 的囊泡,并鉴定了含有 Alcα 或 APP 的囊泡中存在的蛋白质。在这些蛋白质中,Wnt 受体 Frizzled-5 (Fzd5) 主要存在于 Alcα 囊泡中。尽管 Fzd5 在胚胎脑中表达水平较低,因此在分化神经元的神经突中与 Alcα 的共定位比例较低,但 Alcα 表达的抑制降低了 Fzd5 在原代培养神经元神经突中的定位。此外,在原代培养神经元中表达的 Fzd5-EGFP 优先在 Alcα 囊泡的运输速度下在轴突中运输。在表达更高水平 Fzd5 的成年小鼠大脑突触体部分中,Alcα 缺陷型小鼠中 Fzd5 的量和钙/钙调蛋白依赖性蛋白激酶-II 的磷酸化水平降低。这些结果表明,与轴突末端的驱动蛋白-1 相关的 Alcα 囊泡中 Fzd5 的运输减少可能会损害成熟神经元神经末梢中非经典 Ca 依赖性信号转导途径中对 Wnt 配体的反应。