Laboratorio de Imágenes y Visión por Computadora, Instituto de Biotecnología, Universidad Nacional Autónoma de México, Cd. de México, C.P. 04510, Mexico.
Departamento de Ecología Funcional, Instituto de Ecología, Laboratorio de Genética Molecular, Epigenética, Desarrollo y Evolución de Plantas, Universidad Nacional Autónoma de México, Cd. de México, C.P. 04510, Mexico.
Plant Physiol. 2022 Feb 4;188(2):846-860. doi: 10.1093/plphys/kiab530.
Arabidopsis (Arabidopsis thaliana) primary and lateral roots (LRs) are well suited for 3D and 4D microscopy, and their development provides an ideal system for studying morphogenesis and cell proliferation dynamics. With fast-advancing microscopy techniques used for live-imaging, whole tissue data are increasingly available, yet present the great challenge of analyzing complex interactions within cell populations. We developed a plugin "Live Plant Cell Tracking" (LiPlaCeT) coupled to the publicly available ImageJ image analysis program and generated a pipeline that allows, with the aid of LiPlaCeT, 4D cell tracking and lineage analysis of populations of dividing and growing cells. The LiPlaCeT plugin contains ad hoc ergonomic curating tools, making it very simple to use for manual cell tracking, especially when the signal-to-noise ratio of images is low or variable in time or 3D space and when automated methods may fail. Performing time-lapse experiments and using cell-tracking data extracted with the assistance of LiPlaCeT, we accomplished deep analyses of cell proliferation and clonal relations in the whole developing LR primordia and constructed genealogical trees. We also used cell-tracking data for endodermis cells of the root apical meristem (RAM) and performed automated analyses of cell population dynamics using ParaView software (also publicly available). Using the RAM as an example, we also showed how LiPlaCeT can be used to generate information at the whole-tissue level regarding cell length, cell position, cell growth rate, cell displacement rate, and proliferation activity. The pipeline will be useful in live-imaging studies of roots and other plant organs to understand complex interactions within proliferating and growing cell populations. The plugin includes a step-by-step user manual and a dataset example that are available at https://www.ibt.unam.mx/documentos/diversos/LiPlaCeT.zip.
拟南芥(Arabidopsis thaliana)的主根和侧根(LRs)非常适合用于 3D 和 4D 显微镜观察,其发育为研究形态发生和细胞增殖动力学提供了理想的系统。随着用于活细胞成像的显微镜技术的快速发展,越来越多的全组织数据可用,但也带来了分析细胞群体中复杂相互作用的巨大挑战。我们开发了一个名为“活体植物细胞跟踪”(LiPlaCeT)的插件,该插件与公开的 ImageJ 图像分析程序相结合,并生成了一个管道,该管道借助 LiPlaCeT 允许对分裂和生长细胞的群体进行 4D 细胞跟踪和谱系分析。LiPlaCeT 插件包含专门的人体工程学编辑工具,使其非常易于使用手动细胞跟踪,特别是在图像的信噪比低或在时间或 3D 空间中变化时,或者当自动化方法可能失败时。通过进行延时实验并使用 LiPlaCeT 协助提取的细胞跟踪数据,我们完成了整个发育中的 LR 原基中细胞增殖和克隆关系的深入分析,并构建了系谱树。我们还使用细胞跟踪数据对根顶端分生组织(RAM)的内皮层细胞进行了分析,并使用 ParaView 软件(也可公开获得)对细胞群体动态进行了自动分析。以 RAM 为例,我们还展示了如何使用 LiPlaCeT 生成有关细胞长度、细胞位置、细胞生长率、细胞位移率和增殖活性的整个组织水平的信息。该管道将在活体成像研究根和其他植物器官中有用,以了解增殖和生长细胞群体中的复杂相互作用。该插件包括分步用户手册和可在 https://www.ibt.unam.mx/documentos/diversos/LiPlaCeT.zip 上获得的数据集示例。