Methodology for comprehensive cell-level analysis of wound healing experiments using deep learning in MATLAB

Abstract Background Endothelial healing after deployment of cardiovascular devices is particularly important in the context of clinical outcome. It is therefore of great interest to develop tools for a precise prediction of endothelial growth after injury in the process of implant deployment. For ex...

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Main Authors: Jan Oldenburg, Lisa Maletzki, Anne Strohbach, Paul Bellé, Stefan Siewert, Raila Busch, Stephan B. Felix, Klaus-Peter Schmitz, Michael Stiehm
Format: Article
Language:English
Published: BMC 2021-06-01
Series:BMC Molecular and Cell Biology
Subjects:
CNN
Online Access:https://doi.org/10.1186/s12860-021-00369-3
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spelling doaj-475e1edd0f744205a180b1fb1c80034a2021-06-06T11:45:07ZengBMCBMC Molecular and Cell Biology2661-88502021-06-0122111510.1186/s12860-021-00369-3Methodology for comprehensive cell-level analysis of wound healing experiments using deep learning in MATLABJan Oldenburg0Lisa Maletzki1Anne Strohbach2Paul Bellé3Stefan Siewert4Raila Busch5Stephan B. Felix6Klaus-Peter Schmitz7Michael Stiehm8Institute for ImplantTechnology and Biomaterials e.VDepartment of Internal Medicine, Cardiology, University Medicine GreifswaldDepartment of Internal Medicine, Cardiology, University Medicine GreifswaldInstitute for ImplantTechnology and Biomaterials e.VInstitute for ImplantTechnology and Biomaterials e.VDepartment of Internal Medicine, Cardiology, University Medicine GreifswaldDepartment of Internal Medicine, Cardiology, University Medicine GreifswaldInstitute for ImplantTechnology and Biomaterials e.VInstitute for ImplantTechnology and Biomaterials e.VAbstract Background Endothelial healing after deployment of cardiovascular devices is particularly important in the context of clinical outcome. It is therefore of great interest to develop tools for a precise prediction of endothelial growth after injury in the process of implant deployment. For experimental investigation of re-endothelialization in vitro cell migration assays are routinely used. However, semi-automatic analyses of live cell images are often based on gray value distributions and are as such limited by image quality and user dependence. The rise of deep learning algorithms offers promising opportunities for application in medical image analysis. Here, we present an intelligent cell detection (iCD) approach for comprehensive assay analysis to obtain essential characteristics on cell and population scale. Results In an in vitro wound healing assay, we compared conventional analysis methods with our iCD approach. Therefore we determined cell density and cell velocity on cell scale and the movement of the cell layer as well as the gap closure between two cell monolayers on population scale. Our data demonstrate that cell density analysis based on deep learning algorithms is superior to an adaptive threshold method regarding robustness against image distortion. In addition, results on cell scale obtained with iCD are in agreement with manually velocity detection, while conventional methods, such as Cell Image Velocimetry (CIV), underestimate cell velocity by a factor of 0.5. Further, we found that iCD analysis of the monolayer movement gave results just as well as manual freehand detection, while conventional methods again shows more frayed leading edge detection compared to manual detection. Analysis of monolayer edge protrusion by ICD also produced results, which are close to manual estimation with an relative error of 11.7%. In comparison, the conventional Canny method gave a relative error of 76.4%. Conclusion The results of our experiments indicate that deep learning algorithms such as our iCD have the ability to outperform conventional methods in the field of wound healing analysis. The combined analysis on cell and population scale using iCD is very well suited for timesaving and high quality wound healing analysis enabling the research community to gain detailed understanding of endothelial movement.https://doi.org/10.1186/s12860-021-00369-3Endothelial cellsUnetCNNNeural networkWound healingCell scale
collection DOAJ
language English
format Article
sources DOAJ
author Jan Oldenburg
Lisa Maletzki
Anne Strohbach
Paul Bellé
Stefan Siewert
Raila Busch
Stephan B. Felix
Klaus-Peter Schmitz
Michael Stiehm
spellingShingle Jan Oldenburg
Lisa Maletzki
Anne Strohbach
Paul Bellé
Stefan Siewert
Raila Busch
Stephan B. Felix
Klaus-Peter Schmitz
Michael Stiehm
Methodology for comprehensive cell-level analysis of wound healing experiments using deep learning in MATLAB
BMC Molecular and Cell Biology
Endothelial cells
Unet
CNN
Neural network
Wound healing
Cell scale
author_facet Jan Oldenburg
Lisa Maletzki
Anne Strohbach
Paul Bellé
Stefan Siewert
Raila Busch
Stephan B. Felix
Klaus-Peter Schmitz
Michael Stiehm
author_sort Jan Oldenburg
title Methodology for comprehensive cell-level analysis of wound healing experiments using deep learning in MATLAB
title_short Methodology for comprehensive cell-level analysis of wound healing experiments using deep learning in MATLAB
title_full Methodology for comprehensive cell-level analysis of wound healing experiments using deep learning in MATLAB
title_fullStr Methodology for comprehensive cell-level analysis of wound healing experiments using deep learning in MATLAB
title_full_unstemmed Methodology for comprehensive cell-level analysis of wound healing experiments using deep learning in MATLAB
title_sort methodology for comprehensive cell-level analysis of wound healing experiments using deep learning in matlab
publisher BMC
series BMC Molecular and Cell Biology
issn 2661-8850
publishDate 2021-06-01
description Abstract Background Endothelial healing after deployment of cardiovascular devices is particularly important in the context of clinical outcome. It is therefore of great interest to develop tools for a precise prediction of endothelial growth after injury in the process of implant deployment. For experimental investigation of re-endothelialization in vitro cell migration assays are routinely used. However, semi-automatic analyses of live cell images are often based on gray value distributions and are as such limited by image quality and user dependence. The rise of deep learning algorithms offers promising opportunities for application in medical image analysis. Here, we present an intelligent cell detection (iCD) approach for comprehensive assay analysis to obtain essential characteristics on cell and population scale. Results In an in vitro wound healing assay, we compared conventional analysis methods with our iCD approach. Therefore we determined cell density and cell velocity on cell scale and the movement of the cell layer as well as the gap closure between two cell monolayers on population scale. Our data demonstrate that cell density analysis based on deep learning algorithms is superior to an adaptive threshold method regarding robustness against image distortion. In addition, results on cell scale obtained with iCD are in agreement with manually velocity detection, while conventional methods, such as Cell Image Velocimetry (CIV), underestimate cell velocity by a factor of 0.5. Further, we found that iCD analysis of the monolayer movement gave results just as well as manual freehand detection, while conventional methods again shows more frayed leading edge detection compared to manual detection. Analysis of monolayer edge protrusion by ICD also produced results, which are close to manual estimation with an relative error of 11.7%. In comparison, the conventional Canny method gave a relative error of 76.4%. Conclusion The results of our experiments indicate that deep learning algorithms such as our iCD have the ability to outperform conventional methods in the field of wound healing analysis. The combined analysis on cell and population scale using iCD is very well suited for timesaving and high quality wound healing analysis enabling the research community to gain detailed understanding of endothelial movement.
topic Endothelial cells
Unet
CNN
Neural network
Wound healing
Cell scale
url https://doi.org/10.1186/s12860-021-00369-3
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