Kanadome Takashi, Hoshino Natsumi, Nagai Takeharu, Yagi Takeshi, Matsuda Tomoki
Precursory Research for Embryonic Science and Technology (PRESTO), Japan Science and Technology Agency (JST), Kawaguchi, Saitama 332-0012, Japan.
Department of Biomolecular Science and Engineering, SANKEN (The Institute of Scientific and Industrial Research), Osaka University, 8-1 Mihogaoka, Ibaraki 567-0047, Japan.
iScience. 2023 Jul 17;26(7):107238. doi: 10.1016/j.isci.2023.107238. eCollection 2023 Jul 21.
Clustered protocadherin (Pcdh), a cell adhesion protein, is involved in the self-recognition and non-self-discrimination of neurons by conferring diversity on the cell surface. Although the roles of Pcdh in neurons have been elucidated, it has been challenging to visualize its adhesion activity in neurons, which is a molecular function of Pcdh. Here, we present fluorescent indicators, named IPADs, which visualize the interaction of protocadherin-α4 isoform (α4). IPADs successfully visualize not only homophilic α4 -interactions, but also combinatorial homophilic interactions between cells. The reversible nature of IPADs overcomes a drawback of the split-GFP technique and allows for monitoring the dissociation of α4 -interactions. Specially designed IPADs for self-recognition are able to monitor the formation and disruption of α4 -interactions between processes originating from the same neurons. We expect that IPADs will be useful tools for obtaining spatiotemporal information on Pcdh interactions in neuronal self-recognition and non-self-discrimination processes.
成簇原钙黏蛋白(Pcdh)是一种细胞黏附蛋白,通过赋予细胞表面多样性参与神经元的自我识别和非自我识别。尽管Pcdh在神经元中的作用已得到阐明,但可视化其在神经元中的黏附活性一直具有挑战性,而这是Pcdh的一种分子功能。在此,我们展示了名为IPADs的荧光指示剂,其可可视化原钙黏蛋白-α4亚型(α4)的相互作用。IPADs不仅成功地可视化了同嗜性α4相互作用,还能可视化细胞间的组合同嗜性相互作用。IPADs的可逆性克服了分裂GFP技术的一个缺点,并允许监测α4相互作用的解离。专门设计用于自我识别的IPADs能够监测源自同一神经元的突起之间α4相互作用的形成和破坏。我们期望IPADs将成为获取神经元自我识别和非自我识别过程中Pcdh相互作用时空信息的有用工具。