» Articles » PMID: 33424024

A Robust Unsupervised Machine-learning Method to Quantify the Morphological Heterogeneity of Cells and Nuclei

Overview
Journal Nat Protoc
Specialties Biology
Pathology
Science
Date 2021 Jan 11
PMID 33424024
Citations 47
Authors
Affiliations
Soon will be listed here.
Abstract

Cell morphology encodes essential information on many underlying biological processes. It is commonly used by clinicians and researchers in the study, diagnosis, prognosis, and treatment of human diseases. Quantification of cell morphology has seen tremendous advances in recent years. However, effectively defining morphological shapes and evaluating the extent of morphological heterogeneity within cell populations remain challenging. Here we present a protocol and software for the analysis of cell and nuclear morphology from fluorescence or bright-field images using the VAMPIRE algorithm ( https://github.com/kukionfr/VAMPIRE_open ). This algorithm enables the profiling and classification of cells into shape modes based on equidistant points along cell and nuclear contours. Examining the distributions of cell morphologies across automatically identified shape modes provides an effective visualization scheme that relates cell shapes to cellular subtypes based on endogenous and exogenous cellular conditions. In addition, these shape mode distributions offer a direct and quantitative way to measure the extent of morphological heterogeneity within cell populations. This protocol is highly automated and fast, with the ability to quantify the morphologies from 2D projections of cells seeded both on 2D substrates or embedded within 3D microenvironments, such as hydrogels and tissues. The complete analysis pipeline can be completed within 60 minutes for a dataset of ~20,000 cells/2,400 images.

Citing Articles

Profiling DNA damage in 3D Histology Samples.

Penas K, Haeusler R, Feng S, Magidson V, Dmitrieva M, Wink D Med Opt Imaging Virtual Microsc Image Anal (2022). 2025; :84-93.

PMID: 39899002 PMC: 7617225. DOI: 10.1007/978-3-031-16961-8_9.


AI-driven 3D bioprinting for regenerative medicine: From bench to bedside.

Zhang Z, Zhou X, Fang Y, Xiong Z, Zhang T Bioact Mater. 2024; 45:201-230.

PMID: 39651398 PMC: 11625302. DOI: 10.1016/j.bioactmat.2024.11.021.


Microfluidic-Based Electrical Operation and Measurement Methods in Single-Cell Analysis.

Liu X, Zheng X Sensors (Basel). 2024; 24(19).

PMID: 39409403 PMC: 11478560. DOI: 10.3390/s24196359.


A multiparametric analysis including single-cell and subcellular feature assessment reveals differential behavior of spheroid cultures on distinct ultra-low attachment plate types.

Vitacolonna M, Bruch R, Agaci A, Nurnberg E, Cesetti T, Keller F Front Bioeng Biotechnol. 2024; 12:1422235.

PMID: 39157442 PMC: 11327450. DOI: 10.3389/fbioe.2024.1422235.


A systematic evaluation of computational methods for cell segmentation.

Wang Y, Zhao J, Xu H, Han C, Tao Z, Zhou D Brief Bioinform. 2024; 25(5).

PMID: 39154193 PMC: 11330341. DOI: 10.1093/bib/bbae407.


References
1.
Driscoll M, Albanese J, Xiong Z, Mailman M, Losert W, Cao K . Automated image analysis of nuclear shape: what can we learn from a prematurely aged cell?. Aging (Albany NY). 2012; 4(2):119-32. PMC: 3314174. DOI: 10.18632/aging.100434. View

2.
Meijering E, Carpenter A, Peng H, Hamprecht F, Olivo-Marin J . Imagining the future of bioimage analysis. Nat Biotechnol. 2016; 34(12):1250-1255. DOI: 10.1038/nbt.3722. View

3.
Yu Y, Gaillard S, Phillip J, Huang T, Pinto S, Tessarollo N . Inhibition of Spleen Tyrosine Kinase Potentiates Paclitaxel-Induced Cytotoxicity in Ovarian Cancer Cells by Stabilizing Microtubules. Cancer Cell. 2015; 28(1):82-96. PMC: 5257279. DOI: 10.1016/j.ccell.2015.05.009. View

4.
Sarnecki J, Burns K, Wood L, Waters K, Hruban R, Wirtz D . A robust nonlinear tissue-component discrimination method for computational pathology. Lab Invest. 2016; 96(4):450-8. PMC: 4808351. DOI: 10.1038/labinvest.2015.162. View

5.
Jayatilaka H, Tyle P, Chen J, Kwak M, Ju J, Kim H . Synergistic IL-6 and IL-8 paracrine signalling pathway infers a strategy to inhibit tumour cell migration. Nat Commun. 2017; 8:15584. PMC: 5458548. DOI: 10.1038/ncomms15584. View