Chan Zuckerberg Biohub; Department of Bioengineering and Therapeutic Sciences, University of California San Francisco;
Department of Bioengineering and Therapeutic Sciences, University of California San Francisco; Programs in Human Genetics and Biological Sciences, University of California San Francisco;
J Vis Exp. 2023 Jan 20(191). doi: 10.3791/65030.
Asymmetric cell division (ACD), which produces two daughter cells of different fates, is fundamental for generating cellular diversity. In the developing organs of both invertebrates and vertebrates, asymmetrically dividing progenitors generates a Notch self-renewing and a Notch differentiating daughter. In the embryonic zebrafish brain, radial glia progenitors (RGPs)-the principal vertebrate neural stem cells-mostly undergo ACD to give birth to one RGP and one differentiating neuron. The optical clarity and easy accessibility of zebrafish embryos make them ideal for in vivo time-lapse imaging to directly visualize how and when the asymmetry of Notch signaling is established during ACD. Recent studies have shown that dynamic endocytosis of the Notch ligand DeltaD plays a crucial role in cell fate determination during ACD, and the process is regulated by the evolutionarily conserved polarity regulator Par-3 (also known as Pard3) and the dynein motor complex. To visualize the in vivo trafficking patterns of Notch signaling endosomes in mitotic RGPs, we have developed this antibody uptake assay. Using the assay, we have uncovered the dynamicity of DeltaD-containing endosomes during RGP division.
不对称细胞分裂(ACD)产生具有不同命运的两个子细胞,是产生细胞多样性的基础。在无脊椎动物和脊椎动物的发育器官中,不对称分裂的祖细胞产生一个 Notch 自我更新和一个 Notch 分化的子细胞。在胚胎斑马鱼脑中,放射状胶质细胞祖细胞(RGPs)——主要的脊椎动物神经干细胞——主要通过 ACD 产生一个 RGP 和一个分化神经元。斑马鱼胚胎的光学透明度和易于接近性使它们成为体内延时成像的理想选择,可以直接观察 Notch 信号不对称性在 ACD 期间是如何以及何时建立的。最近的研究表明,Notch 配体 DeltaD 的动态内吞作用在 ACD 期间的细胞命运决定中起着至关重要的作用,该过程受进化保守的极性调节剂 Par-3(也称为 Pard3)和动力蛋白复合物的调节。为了可视化有丝分裂 RGPs 中 Notch 信号内体的体内运输模式,我们开发了这种抗体摄取测定法。使用该测定法,我们揭示了 RGP 分裂过程中含有 DeltaD 的内体的动态性。