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Quantification of Osteoclasts in Culture, Powered by Machine Learning

In vitro osteoclastogenesis is a central assay in bone biology to study the effect of genetic and pharmacologic cues on the differentiation of bone resorbing osteoclasts. To date, identification of TRAP+ multinucleated cells and measurements of osteoclast number and surface rely on a manual tracing...

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Autores principales: Cohen-Karlik, Edo, Awida, Zamzam, Bergman, Ayelet, Eshed, Shahar, Nestor, Omer, Kadashev, Michelle, Yosef, Sapir Ben, Saed, Hussam, Mansour, Yishay, Globerson, Amir, Neumann, Drorit, Gabet, Yankel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8186397/
https://www.ncbi.nlm.nih.gov/pubmed/34113621
http://dx.doi.org/10.3389/fcell.2021.674710
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author Cohen-Karlik, Edo
Awida, Zamzam
Bergman, Ayelet
Eshed, Shahar
Nestor, Omer
Kadashev, Michelle
Yosef, Sapir Ben
Saed, Hussam
Mansour, Yishay
Globerson, Amir
Neumann, Drorit
Gabet, Yankel
author_facet Cohen-Karlik, Edo
Awida, Zamzam
Bergman, Ayelet
Eshed, Shahar
Nestor, Omer
Kadashev, Michelle
Yosef, Sapir Ben
Saed, Hussam
Mansour, Yishay
Globerson, Amir
Neumann, Drorit
Gabet, Yankel
author_sort Cohen-Karlik, Edo
collection PubMed
description In vitro osteoclastogenesis is a central assay in bone biology to study the effect of genetic and pharmacologic cues on the differentiation of bone resorbing osteoclasts. To date, identification of TRAP+ multinucleated cells and measurements of osteoclast number and surface rely on a manual tracing requiring specially trained lab personnel. This task is tedious, time-consuming, and prone to operator bias. Here, we propose to replace this laborious manual task with a completely automatic process using algorithms developed for computer vision. To this end, we manually annotated full cultures by contouring each cell, and trained a machine learning algorithm to detect and classify cells into preosteoclast (TRAP+ cells with 1–2 nuclei), osteoclast type I (cells with more than 3 nuclei and less than 15 nuclei), and osteoclast type II (cells with more than 15 nuclei). The training usually requires thousands of annotated samples and we developed an approach to minimize this requirement. Our novel strategy was to train the algorithm by working at “patch-level” instead of on the full culture, thus amplifying by >20-fold the number of patches to train on. To assess the accuracy of our algorithm, we asked whether our model measures osteoclast number and area at least as well as any two trained human annotators. The results indicated that for osteoclast type I cells, our new model achieves a Pearson correlation (r) of 0.916 to 0.951 with human annotators in the estimation of osteoclast number, and 0.773 to 0.879 for estimating the osteoclast area. Because the correlation between 3 different trained annotators ranged between 0.948 and 0.958 for the cell count and between 0.915 and 0.936 for the area, we can conclude that our trained model is in good agreement with trained lab personnel, with a correlation that is similar to inter-annotator correlation. Automation of osteoclast culture quantification is a useful labor-saving and unbiased technique, and we suggest that a similar machine-learning approach may prove beneficial for other morphometrical analyses.
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spelling pubmed-81863972021-06-09 Quantification of Osteoclasts in Culture, Powered by Machine Learning Cohen-Karlik, Edo Awida, Zamzam Bergman, Ayelet Eshed, Shahar Nestor, Omer Kadashev, Michelle Yosef, Sapir Ben Saed, Hussam Mansour, Yishay Globerson, Amir Neumann, Drorit Gabet, Yankel Front Cell Dev Biol Cell and Developmental Biology In vitro osteoclastogenesis is a central assay in bone biology to study the effect of genetic and pharmacologic cues on the differentiation of bone resorbing osteoclasts. To date, identification of TRAP+ multinucleated cells and measurements of osteoclast number and surface rely on a manual tracing requiring specially trained lab personnel. This task is tedious, time-consuming, and prone to operator bias. Here, we propose to replace this laborious manual task with a completely automatic process using algorithms developed for computer vision. To this end, we manually annotated full cultures by contouring each cell, and trained a machine learning algorithm to detect and classify cells into preosteoclast (TRAP+ cells with 1–2 nuclei), osteoclast type I (cells with more than 3 nuclei and less than 15 nuclei), and osteoclast type II (cells with more than 15 nuclei). The training usually requires thousands of annotated samples and we developed an approach to minimize this requirement. Our novel strategy was to train the algorithm by working at “patch-level” instead of on the full culture, thus amplifying by >20-fold the number of patches to train on. To assess the accuracy of our algorithm, we asked whether our model measures osteoclast number and area at least as well as any two trained human annotators. The results indicated that for osteoclast type I cells, our new model achieves a Pearson correlation (r) of 0.916 to 0.951 with human annotators in the estimation of osteoclast number, and 0.773 to 0.879 for estimating the osteoclast area. Because the correlation between 3 different trained annotators ranged between 0.948 and 0.958 for the cell count and between 0.915 and 0.936 for the area, we can conclude that our trained model is in good agreement with trained lab personnel, with a correlation that is similar to inter-annotator correlation. Automation of osteoclast culture quantification is a useful labor-saving and unbiased technique, and we suggest that a similar machine-learning approach may prove beneficial for other morphometrical analyses. Frontiers Media S.A. 2021-05-25 /pmc/articles/PMC8186397/ /pubmed/34113621 http://dx.doi.org/10.3389/fcell.2021.674710 Text en Copyright © 2021 Cohen-Karlik, Awida, Bergman, Eshed, Nestor, Kadashev, Yosef, Saed, Mansour, Globerson, Neumann and Gabet. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Cell and Developmental Biology
Cohen-Karlik, Edo
Awida, Zamzam
Bergman, Ayelet
Eshed, Shahar
Nestor, Omer
Kadashev, Michelle
Yosef, Sapir Ben
Saed, Hussam
Mansour, Yishay
Globerson, Amir
Neumann, Drorit
Gabet, Yankel
Quantification of Osteoclasts in Culture, Powered by Machine Learning
title Quantification of Osteoclasts in Culture, Powered by Machine Learning
title_full Quantification of Osteoclasts in Culture, Powered by Machine Learning
title_fullStr Quantification of Osteoclasts in Culture, Powered by Machine Learning
title_full_unstemmed Quantification of Osteoclasts in Culture, Powered by Machine Learning
title_short Quantification of Osteoclasts in Culture, Powered by Machine Learning
title_sort quantification of osteoclasts in culture, powered by machine learning
topic Cell and Developmental Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8186397/
https://www.ncbi.nlm.nih.gov/pubmed/34113621
http://dx.doi.org/10.3389/fcell.2021.674710
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