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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...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2021
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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. |
format | Online Article Text |
id | pubmed-8186397 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
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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