PUBLICATION

LongAxis: A MATLAB-based program for 3D quantitative analysis of epithelial cell shape and orientation

Authors
Carney, K.R., Bryan, C.D., Gordon, H.B., Kwan, K.M.
ID
ZDB-PUB-200221-43
Date
2020
Source
Developmental Biology   458: 1-11 (Journal)
Registered Authors
Kwan, Kristen
Keywords
Extracellular matrix, Eye, MATLAB, Morphology, Neural retina, Polarity
MeSH Terms
  • Animals
  • Animals, Genetically Modified
  • Carrier Proteins/genetics
  • Carrier Proteins/metabolism
  • Cell Shape*
  • Epithelial Cells*/cytology
  • Epithelial Cells*/metabolism
  • Image Processing, Computer-Assisted*
  • Laminin/genetics
  • Laminin/metabolism
  • Retina*/cytology
  • Retina*/embryology
  • Software*
  • Zebrafish/embryology*
  • Zebrafish/genetics
  • Zebrafish Proteins/genetics
  • Zebrafish Proteins/metabolism
PubMed
31589834 Full text @ Dev. Biol.
Abstract
Epithelial morphogenesis, a fundamental aspect of development, generates 3-dimensional tissue structures crucial for organ function. Underlying morphogenetic mechanisms are, in many cases, poorly understood, but mutations that perturb organ development can affect epithelial cell shape and orientation - difficult features to quantify in three dimensions. The basic structure of the eye is established via epithelial morphogenesis: in the embryonic optic cup, the retinal progenitor epithelium enwraps the lens. We previously found that loss of the extracellular matrix protein laminin-alpha1 (lama1) led to mislocalization of apical polarity markers and apparent misorientation of retinal progenitors. We sought to visualize and quantify this phenotype, and determine whether loss of the apical polarity determinant pard3 might rescue the phenotype. To this end, we developed LongAxis, a MATLAB-based program optimized for the retinal progenitor neuroepithelium. LongAxis facilitates 3-dimensional cell segmentation, visualization, and quantification of cell orientation and morphology. Using LongAxis, we find that retinal progenitors in the lama1-/- optic cup are misoriented and slightly less elongated. In the lama1;MZpard3 double mutant, cells are still misoriented, but larger. Therefore, loss of pard3 does not rescue loss of lama1, and in fact uncovers a novel cell size phenotype. LongAxis enables population-level visualization and quantification of retinal progenitor cell orientation and morphology. These results underscore the importance of visualizing and quantifying cell orientation and shape in three dimensions within the retina.
Genes / Markers
Figures
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Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Antibodies
Orthology
Engineered Foreign Genes
Mapping