MUSCLEMOTION: a versatile open software tool to quantify cardiomyocyte and cardiac muscle contraction in vitro and in vivo

Rationale: There are several methods to measure cardiomyocyte (CM) and muscle contraction but these require customized hardware, expensive apparatus and advanced informatics or can only be used in single experimental models. Consequently, data and techniques have been difficult to reproduce across m...

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Main Authors: Sala, L., van Meer, B.J., Tertoolen, L.G.J., Bakkers, J., Bellin, M., Davis, R.P., Denning, Chris, Dieben, M.A.E., Eschenhagen, T., Giacomelli, E., Grandela, C., Hansen, A., Holman, E.R., Jongbloed, M.R.M., Kamel, S.M., Koopman, C.D., Lachaud, Q., Mannhardt, I., Mol, M.P.H., Mosqueira, D., Orlova, V.V., Passier, R., Ribeiro, M.C., Saleem, U., Smith, G.L., Mummery, C.L., Burton, F.L.
Format: Article
Published: American Heart Association 2017
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Online Access:https://eprints.nottingham.ac.uk/48987/
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author Sala, L.
van Meer, B.J.
Tertoolen, L.G.J.
Bakkers, J.
Bellin, M.
Davis, R.P.
Denning, Chris
Dieben, M.A.E.
Eschenhagen, T.
Giacomelli, E.
Grandela, C.
Hansen, A.
Holman, E.R.
Jongbloed, M.R.M.
Kamel, S.M.
Koopman, C.D.
Lachaud, Q.
Mannhardt, I.
Mol, M.P.H.
Mosqueira, D.
Orlova, V.V.
Passier, R.
Ribeiro, M.C.
Saleem, U.
Smith, G.L.
Mummery, C.L.
Burton, F.L.
author_facet Sala, L.
van Meer, B.J.
Tertoolen, L.G.J.
Bakkers, J.
Bellin, M.
Davis, R.P.
Denning, Chris
Dieben, M.A.E.
Eschenhagen, T.
Giacomelli, E.
Grandela, C.
Hansen, A.
Holman, E.R.
Jongbloed, M.R.M.
Kamel, S.M.
Koopman, C.D.
Lachaud, Q.
Mannhardt, I.
Mol, M.P.H.
Mosqueira, D.
Orlova, V.V.
Passier, R.
Ribeiro, M.C.
Saleem, U.
Smith, G.L.
Mummery, C.L.
Burton, F.L.
author_sort Sala, L.
building Nottingham Research Data Repository
collection Online Access
description Rationale: There are several methods to measure cardiomyocyte (CM) and muscle contraction but these require customized hardware, expensive apparatus and advanced informatics or can only be used in single experimental models. Consequently, data and techniques have been difficult to reproduce across models and laboratories, analysis is time consuming and only specialist researchers can quantify data. Objective: Here we describe and validate an automated, open source software tool (MUSCLEMOTION) adaptable for use with standard laboratory- and clinical imaging equipment that enables quantitative analysis of normal cardiac contraction, disease phenotypes and pharmacological responses. Methods and Results: MUSCLEMOTION allowed rapid and easy measurement of contractility from high-speed movies in: (i) 1-dimensional in vitro models such as isolated adult and human pluripotent stem cell-derived CMs (hPSC-CMs); (ii) 2-dimensional in vitro models, such as beating CM monolayers or small clusters of hPSC-CMs; (iii) 3-dimensional multicellular in vitro or in vivo contractile tissues such as cardiac "organoids", engineered heart tissues (EHT), zebrafish- and human hearts. MUSCLEMOTION was effective under different recording conditions (bright field microscopy with simultaneous patch clamp recording, phase contrast microscopy and traction force microscopy). Outcomes were virtually identical to the current gold standards for contraction measurement such as optical flow, pole deflection, edge-detection systems or manual analyses. Finally, we used the algorithm to quantify contraction in in vitro and in vivo arrhythmia models and to measure pharmacological responses. Conclusions: Using a single open source method for processing video recordings, we obtained reliable pharmacological data and measures of cardiac disease phenotype in experimental cell-, animal- and human models
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spelling nottingham-489872020-05-04T19:24:07Z https://eprints.nottingham.ac.uk/48987/ MUSCLEMOTION: a versatile open software tool to quantify cardiomyocyte and cardiac muscle contraction in vitro and in vivo Sala, L. van Meer, B.J. Tertoolen, L.G.J. Bakkers, J. Bellin, M. Davis, R.P. Denning, Chris Dieben, M.A.E. Eschenhagen, T. Giacomelli, E. Grandela, C. Hansen, A. Holman, E.R. Jongbloed, M.R.M. Kamel, S.M. Koopman, C.D. Lachaud, Q. Mannhardt, I. Mol, M.P.H. Mosqueira, D. Orlova, V.V. Passier, R. Ribeiro, M.C. Saleem, U. Smith, G.L. Mummery, C.L. Burton, F.L. Rationale: There are several methods to measure cardiomyocyte (CM) and muscle contraction but these require customized hardware, expensive apparatus and advanced informatics or can only be used in single experimental models. Consequently, data and techniques have been difficult to reproduce across models and laboratories, analysis is time consuming and only specialist researchers can quantify data. Objective: Here we describe and validate an automated, open source software tool (MUSCLEMOTION) adaptable for use with standard laboratory- and clinical imaging equipment that enables quantitative analysis of normal cardiac contraction, disease phenotypes and pharmacological responses. Methods and Results: MUSCLEMOTION allowed rapid and easy measurement of contractility from high-speed movies in: (i) 1-dimensional in vitro models such as isolated adult and human pluripotent stem cell-derived CMs (hPSC-CMs); (ii) 2-dimensional in vitro models, such as beating CM monolayers or small clusters of hPSC-CMs; (iii) 3-dimensional multicellular in vitro or in vivo contractile tissues such as cardiac "organoids", engineered heart tissues (EHT), zebrafish- and human hearts. MUSCLEMOTION was effective under different recording conditions (bright field microscopy with simultaneous patch clamp recording, phase contrast microscopy and traction force microscopy). Outcomes were virtually identical to the current gold standards for contraction measurement such as optical flow, pole deflection, edge-detection systems or manual analyses. Finally, we used the algorithm to quantify contraction in in vitro and in vivo arrhythmia models and to measure pharmacological responses. Conclusions: Using a single open source method for processing video recordings, we obtained reliable pharmacological data and measures of cardiac disease phenotype in experimental cell-, animal- and human models American Heart Association 2017-12-27 Article PeerReviewed Sala, L., van Meer, B.J., Tertoolen, L.G.J., Bakkers, J., Bellin, M., Davis, R.P., Denning, Chris, Dieben, M.A.E., Eschenhagen, T., Giacomelli, E., Grandela, C., Hansen, A., Holman, E.R., Jongbloed, M.R.M., Kamel, S.M., Koopman, C.D., Lachaud, Q., Mannhardt, I., Mol, M.P.H., Mosqueira, D., Orlova, V.V., Passier, R., Ribeiro, M.C., Saleem, U., Smith, G.L., Mummery, C.L. and Burton, F.L. (2017) MUSCLEMOTION: a versatile open software tool to quantify cardiomyocyte and cardiac muscle contraction in vitro and in vivo. Circulation Research . ISSN 0009-7330 Pluripotent stem Cell-derived cardiomyocytes contraction basic science; arrhythmia software tools http://circres.ahajournals.org/content/early/2017/12/26/CIRCRESAHA.117.312067 doi:10.1161/CIRCRESAHA.117.312067 doi:10.1161/CIRCRESAHA.117.312067
spellingShingle Pluripotent stem Cell-derived cardiomyocytes
contraction
basic science; arrhythmia
software tools
Sala, L.
van Meer, B.J.
Tertoolen, L.G.J.
Bakkers, J.
Bellin, M.
Davis, R.P.
Denning, Chris
Dieben, M.A.E.
Eschenhagen, T.
Giacomelli, E.
Grandela, C.
Hansen, A.
Holman, E.R.
Jongbloed, M.R.M.
Kamel, S.M.
Koopman, C.D.
Lachaud, Q.
Mannhardt, I.
Mol, M.P.H.
Mosqueira, D.
Orlova, V.V.
Passier, R.
Ribeiro, M.C.
Saleem, U.
Smith, G.L.
Mummery, C.L.
Burton, F.L.
MUSCLEMOTION: a versatile open software tool to quantify cardiomyocyte and cardiac muscle contraction in vitro and in vivo
title MUSCLEMOTION: a versatile open software tool to quantify cardiomyocyte and cardiac muscle contraction in vitro and in vivo
title_full MUSCLEMOTION: a versatile open software tool to quantify cardiomyocyte and cardiac muscle contraction in vitro and in vivo
title_fullStr MUSCLEMOTION: a versatile open software tool to quantify cardiomyocyte and cardiac muscle contraction in vitro and in vivo
title_full_unstemmed MUSCLEMOTION: a versatile open software tool to quantify cardiomyocyte and cardiac muscle contraction in vitro and in vivo
title_short MUSCLEMOTION: a versatile open software tool to quantify cardiomyocyte and cardiac muscle contraction in vitro and in vivo
title_sort musclemotion: a versatile open software tool to quantify cardiomyocyte and cardiac muscle contraction in vitro and in vivo
topic Pluripotent stem Cell-derived cardiomyocytes
contraction
basic science; arrhythmia
software tools
url https://eprints.nottingham.ac.uk/48987/
https://eprints.nottingham.ac.uk/48987/
https://eprints.nottingham.ac.uk/48987/