Leibniz-Forschungsinstitut Für Molekulare Pharmakologie (FMP), Robert-Roessle-Straße 10, Berlin, 13125, Germany.
Present address: EU-OPENSCREEN ERIC, Robert-Roessle-Straße 10, Berlin, 13125, Germany.
BMC Biol. 2024 Sep 30;22(1):220. doi: 10.1186/s12915-024-02015-8.
Eukaryotic cells are highly compartmentalized by a variety of organelles that carry out specific cellular processes. The position of these organelles within the cell is elaborately regulated and vital for their function. For instance, the position of lysosomes relative to the nucleus controls their degradative capacity and is altered in pathophysiological conditions. The molecular components orchestrating the precise localization of organelles remain incompletely understood. A confounding factor in these studies is the fact that organelle positioning is surprisingly non-trivial to address e.g., perturbations that affect the localization of organelles often lead to secondary phenotypes such as changes in cell or organelle size. These phenotypes could potentially mask effects or lead to the identification of false positive hits. To uncover and test potential molecular components at scale, accurate and easy-to-use analysis tools are required that allow robust measurements of organelle positioning.
Here, we present an analysis workflow for the faithful, robust, and quantitative analysis of organelle positioning phenotypes. Our workflow consists of an easy-to-use Fiji plugin and an R Shiny App. These tools enable users without background in image or data analysis to (1) segment single cells and nuclei and to detect organelles, (2) to measure cell size and the distance between detected organelles and the nucleus, (3) to measure intensities in the organelle channel plus one additional channel, (4) to measure radial intensity profiles of organellar markers, and (5) to plot the results in informative graphs. Using simulated data and immunofluorescent images of cells in which the function of known factors for lysosome positioning has been perturbed, we show that the workflow is robust against common problems for the accurate assessment of organelle positioning such as changes of cell shape and size, organelle size and background.
OrgaMapper is a versatile, robust, and easy-to-use automated image analysis workflow that can be utilized in microscopy-based hypothesis testing and screens. It effectively allows for the mapping of the intracellular space and enables the discovery of novel regulators of organelle positioning.
真核细胞通过各种细胞器进行高度分隔,这些细胞器执行特定的细胞过程。这些细胞器在细胞内的位置受到精心调节,对它们的功能至关重要。例如,溶酶体相对于核的位置控制其降解能力,并在病理生理条件下发生改变。协调细胞器精确定位的分子成分仍不完全清楚。在这些研究中,一个令人困惑的因素是细胞器定位的复杂性,例如,影响细胞器定位的扰动通常会导致次级表型,如细胞或细胞器大小的变化。这些表型可能掩盖效应或导致假阳性命中的识别。为了大规模发现和测试潜在的分子成分,需要精确且易于使用的分析工具,这些工具可以对细胞器定位进行稳健的测量。
在这里,我们提出了一种用于忠实、稳健和定量分析细胞器定位表型的分析工作流程。我们的工作流程包括一个易于使用的 Fiji 插件和一个 R Shiny 应用程序。这些工具使没有图像处理或数据分析背景的用户能够(1)分割单个细胞和细胞核并检测细胞器,(2)测量细胞大小以及检测到的细胞器与细胞核之间的距离,(3)测量细胞器通道和一个附加通道的强度,(4)测量细胞器标记物的径向强度分布,以及(5)在信息丰富的图形中绘制结果。使用模拟数据和已扰动已知溶酶体定位因子功能的细胞的免疫荧光图像,我们表明该工作流程能够稳健地应对准确评估细胞器定位的常见问题,例如细胞形状和大小、细胞器大小和背景的变化。
OrgaMapper 是一种通用、稳健且易于使用的自动化图像分析工作流程,可用于基于显微镜的假设检验和筛选。它有效地允许对细胞内空间进行映射,并能够发现新的细胞器定位调节剂。