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Passive myocardial mechanical properties: meaning, measurement, models

Abstract:
The use of a video method based on the Digital Image Correlation (DIC) algorithm from experimental mechanics to estimate the displacements, strain field, and sarcolemma length in a beating single-cell cardiomyocyte is proposed in this work. The obtained deformation is then correlated with the calcium signal, from calcium imaging where fluorescent dyes sensitive to calcium Ca2+ are used. Our proposed video-based method for simultaneous contraction and intracellular calcium analysis results in a low-cost, non-invasive, and label-free method. This technique has shown great advantages in long-term observations because this type of intervention-free measurement neutralizes the possible alteration in the beating cardiomyocyte introduced by other techniques for measuring cell contractility (e.g., Traction Force Microscopy, Atomic Force Microscopy, Microfabrication or Optical tweezers). Three tests were performed with synthetically augmented data from cardiomyocyte images to validate the robustness of the algorithm. First, a simulated rigid translation of a referenced image is applied, then a rotation, and finally a controlled longitudinal deformation of the referenced image, thus simulating a native realistic deformation. Finally, the proposed framework is evaluated with real experimental data. To validate contraction induced by intracellular calcium concentration, this signal is correlated with a new deformation measure proposed in this article, which is independent of cell orientation in the imaging setup. Finally, based on the displacements obtained by the DIC algorithm, the change in sarcolemma length in a contracting cardiomyocyte is calculated and its temporal correlation with the calcium signal is obtained.This research was funded by the Spanish Ministry of Science and Innovation, grant numbers: PID2020-116927RB-C21, PID2020-116927RB-C22 and PID2023-152610OB-C21.Peer ReviewedPostprint (published version
Publication status:
Published
Peer review status:
Peer reviewed

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Author
ORCID:
0000-0003-1832-6976
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Role:
Author
ORCID:
0000-0002-6773-9884
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Author
ORCID:
0000-0003-2044-8307
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Author
ORCID:
0000-0002-0452-0308
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Role:
Author
ORCID:
0000-0002-6466-4936


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Funder identifier:
10.13039/501100001659
Grant:
#422681845


Publisher:
Springer
Journal:
Biophysical Reviews More from this journal
Volume:
13
Issue:
5
Pages:
587-610
Publication date:
2021-10-13
DOI:
EISSN:
1867-2469
ISSN:
1867-2450


Language:
English
Keywords:
Pubs id:
1249765
Local pid:
pubs:1249765
Source identifiers:
W3210718651
Deposit date:
2026-04-23
ARK identifier:
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