g and Michelle Heeney for their comments on the manuscript. We thank Richard Smith (John Innes Centre, UK) for his advice on image processing. Data availability statement The datasets presented in this study can be found in online repositories. The names of the repository/repositories and accession number(s) can be found below: https://doi.org/10.17605/OSF.IO/UMW9B , https://doi.org/10.17605/OSF.IO/P5Q39 . Author contributions AS: Conceptualization, Data curation, Formal analysis, Investigation, Methodology, Validation, Visualization, Writing – original draft, Writing – review & editing. AR: Conceptualization, Data curation, Funding acquisition, Project administration, Supervision, Writin
Open resource ↗OSF · 10.17605/OSF.IO/UMW9B · lines:234-260Unverified paper record
An optimized live imaging and multiple cell layer growth analysis approach using Arabidopsis sepals.
Frontiers in plant science · 3 Sept 2024 · 10.3389/fpls.2024.1449195
Abstract
Arabidopsis thaliana sepals are excellent models for analyzing growth of entire organs due to their relatively small size, which can be captured at a cellular resolution under a confocal microscope. To investigate how differential growth of connected cell layers generate unique organ morphologies, it is necessary to live-image deep into the tissue. However, imaging deep cell layers of the sepal (or plant tissues in general) is practically challenging. Image processing is also difficult due to the low signal-to-noise ratio of the deeper tissue layers, an issue mainly associated with live imaging datasets. Addressing some of these challenges, we provide an optimized methodology for live imaging sepals, and subsequent image processing. For live imaging early-stage sepals, we found that the use of a bright fluorescent membrane marker, coupled with increased laser intensity and an enhanced Z- resolution produces high-quality images suitable for downstream image processing. Our optimized parameters allowed us to image the bottommost cell layer of the sepal (inner epidermal layer) without compromising viability. We used a 'voxel removal' technique to visualize the inner epidermal layer in MorphoGraphX image processing software. We also describe the MorphoGraphX parameters for creating a 2.5D mesh surface for the inner epidermis. Our parameters allow for the segmentation and parent tracking of individual cells through multiple time points, despite the weak signal of the inner epidermal cells. While we have used sepals to illustrate our approach, the methodology will be useful for researchers intending to live-image and track growth of deeper cell layers in 2.5D for any plant tissue.
Plant phenotyping relevance
植物組織の深部をライブイメージングし、画像処理・細胞セグメンテーション・追跡によって成長を解析する方法自体が中心的に開発・最適化されているため。
abstractwe provide an optimized methodology for live imaging sepals, and subsequent image processing.
abstractOur parameters allow for the segmentation and parent tracking of individual cells through multiple time points
Code and data availability
The paper's Data availability statement deposits the study's datasets (live-imaging/phenotyping data underlying the sepal growth analysis) in two public OSF repositories with explicit DOIs, making them paper-specific, public, and actionable.
on the manuscript. We thank Richard Smith (John Innes Centre, UK) for his advice on image processing. Data availability statement The datasets presented in this study can be found in online repositories. The names of the repository/repositories and accession number(s) can be found below: https://doi.org/10.17605/OSF.IO/UMW9B , https://doi.org/10.17605/OSF.IO/P5Q39 . Author contributions AS: Conceptualization, Data curation, Formal analysis, Investigation, Methodology, Validation, Visualization, Writing – original draft, Writing – review & editing. AR: Conceptualization, Data curation, Funding acquisition, Project administration, Supervision, Writing – review & editing. Conflict of intere
Open resource ↗OSF · 10.17605/OSF.IO/P5Q39 · lines:234-260This is an automatically classified, unverified record. Curator approval is required before any resource enters the Catalog.