Inferring statistical properties of 3D cell geometry from 2D slices

被引:9
|
作者
Sharp, Tristan A. [1 ]
Merkel, Matthias [2 ]
Manning, M. Lisa [2 ,3 ]
Liu, Andrea J. [1 ]
机构
[1] Univ Penn, Dept Phys & Astron, Philadelphia, PA 19104 USA
[2] Syracuse Univ, Phys Dept, Syracuse, NY USA
[3] Syracuse Biomat Inst, Syracuse, NY USA
来源
PLOS ONE | 2019年 / 14卷 / 02期
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
GRAIN-SIZE; RECONSTRUCTION; SEGMENTATION; DYNAMICS; MEDIA; MODEL;
D O I
10.1371/journal.pone.0209892
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Although cell shape can reflect the mechanical and biochemical properties of the cell and its environment, quantification of 3D cell shapes within 3D tissues remains difficult, typically requiring digital reconstruction from a stack of 2D images. We investigate a simple alternative technique to extract information about the 3D shapes of cells in a tissue; this technique connects the ensemble of 3D shapes in the tissue with the distribution of 2D shapes observed in independent 2D slices. Using cell vertex model geometries, we find that the distribution of 2D shapes allows clear determination of the mean value of a 3D shape index. We analyze the errors that may arise in practice in the estimation of the mean 3D shape index from 2D imagery and find that typically only a few dozen cells in 2D imagery are required to reduce uncertainty below 2%. Even though we developed the method for isotropic animal tissues, we demonstrate it on an anisotropic plant tissue. This framework could also be naturally extended to estimate additional 3D geometric features and quantify their uncertainty in other materials.
引用
收藏
页数:18
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