Green Rebecca M, Lo Vercio Lucas D, Dauter Andreas, Barretto Elizabeth C, Devine Jay, Vidal-García Marta, Marchini Marta, Robertson Samuel, Zhao Xiang, Mahika Anandita, Shakir M Bilal, Guo Sienna, Boughner Julia C, Dean Wendy, Lander Arthur D, Marcucio Ralph S, Forkert Nils D, Hallgrímsson Benedikt
Department of Oral and Craniofacial Sciences, Center for Craniofacial and Dental Genetics, University of Pittsburgh, Pittsburgh, PA, United States.
Department of Cell Biology & Anatomy, Cumming School of Medicine, University of Calgary, Calgary, AB, Canada.
bioRxiv. 2023 May 12:2023.05.12.540515. doi: 10.1101/2023.05.12.540515.
Morphogenesis requires highly coordinated, complex interactions between cellular processes: proliferation, migration, and apoptosis, along with physical tissue interactions. How these cellular and tissue dynamics drive morphogenesis remains elusive. Three dimensional (3D) microscopic imaging poses great promise, and generates elegant images. However, generating even moderate through-put quantified images is challenging for many reasons. As a result, the association between morphogenesis and cellular processes in 3D developing tissues has not been fully explored. To address this critical gap, we have developed an imaging and image analysis pipeline to enable 3D quantification of cellular dynamics along with 3D morphology for the same individual embryo. Specifically, we focus on how 3D distribution of proliferation relates to morphogenesis during mouse facial development. Our method involves imaging with light-sheet microscopy, automated segmentation of cells and tissues using machine learning-based tools, and quantification of external morphology via geometric morphometrics. Applying this framework, we show that changes in proliferation are tightly correlated to changes in morphology over the course of facial morphogenesis. These analyses illustrate the potential of this pipeline to investigate mechanistic relationships between cellular dynamics and morphogenesis during embryonic development.
形态发生需要细胞过程之间高度协调、复杂的相互作用:增殖、迁移和凋亡,以及物理组织相互作用。这些细胞和组织动力学如何驱动形态发生仍然难以捉摸。三维(3D)显微成像前景广阔,并能生成精美的图像。然而,由于多种原因,生成即使是适度通量的定量图像也具有挑战性。因此,三维发育组织中形态发生与细胞过程之间的关联尚未得到充分探索。为了填补这一关键空白,我们开发了一种成像和图像分析流程,以实现对同一胚胎个体的细胞动力学进行三维定量以及三维形态分析。具体而言,我们关注在小鼠面部发育过程中增殖的三维分布与形态发生之间的关系。我们的方法包括使用光片显微镜成像、使用基于机器学习的工具对细胞和组织进行自动分割,以及通过几何形态测量学对外部形态进行定量。应用这个框架,我们表明在面部形态发生过程中,增殖的变化与形态的变化紧密相关。这些分析说明了该流程在研究胚胎发育过程中细胞动力学与形态发生之间的机制关系方面的潜力。