Laumonnerie Christophe, Shamambo Maleelo, Stabley Daniel R, Lewis Tommy L, Trivedi Niraj, Howell Danielle, Solecki David J
Neuronal Cell Biology Division, Department of Developmental Neurobiology, St. Jude Children's Research Hospital, 262 Danny Thomas Place, Memphis, TN, 38104, USA.
Aging & Metabolism Program, Oklahoma Medical Research Foundation, 825 NE 13th Street, Oklahoma City, OK, 73104, USA.
Nat Commun. 2025 Jan 7;16(1):355. doi: 10.1038/s41467-024-55400-w.
Exiting a germinal zone (GZ) initiates a cascade of events that promote neuronal maturation and circuit assembly. Developing neurons and their progenitors must interpret various niche signals-such as morphogens, guidance molecules, extracellular matrix components, and adhesive cues-to navigate this region. How differentiating neurons in mouse brains integrate and adapt to multiple cell-extrinsic niche cues with their cell-intrinsic machinery in exiting a GZ is unknown. We establish cooperation between cell polarity-regulated adhesion and Netrin-1 signaling comprises a coincidence detection circuit repelling maturing neurons from their GZ. In this circuit, the Partitioning defective 3 (Pard3) polarity protein and Junctional adhesion molecule-C (JamC) adhesion molecule promote, while the Seven in absentia 2 (Siah2) ubiquitin ligase inhibits, Deleted in colorectal cancer (Dcc) receptor surface recruitment to gate differentiation linked repulsion to GZ Netrin-1. These results demonstrate cell polarity as a central integrator of adhesive- and guidance cues cooperating to spur GZ exit.
离开生发区(GZ)会引发一系列促进神经元成熟和神经回路组装的事件。发育中的神经元及其祖细胞必须解读各种微环境信号,如形态发生素、导向分子、细胞外基质成分和黏附线索,以便在这个区域导航。小鼠大脑中正在分化的神经元如何利用其细胞内在机制整合并适应多种细胞外微环境线索从而离开生发区,目前尚不清楚。我们发现细胞极性调节的黏附与Netrin-1信号传导之间的协同作用构成了一个巧合检测回路,将成熟神经元从生发区排斥出去。在这个回路中,分区缺陷3(Pard3)极性蛋白和连接黏附分子C(JamC)黏附分子起促进作用,而无七同源物2(Siah2)泛素连接酶起抑制作用,结肠直肠癌缺失基因(Dcc)受体的表面募集会控制与生发区Netrin-1相关的分化连接排斥。这些结果表明细胞极性是黏附线索和导向线索协同作用以刺激生发区退出的核心整合因子。