Revealing the nanometric structural changes in myocardial infarction models by time-lapse intravital imaging

In the development of bioinspired nanomaterials for therapeutic applications, it is very important to validate the design of nanomaterials in the disease models. Therefore, it is desirable to visualize the change of the cells in the diseased site at the nanoscale. Heart diseases often start with str...

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Main Authors: Chiung Wen Kuo, Feby Wijaya Pratiwi, Yen-Ting Liu, Di-Yen Chueh, Peilin Chen
Format: Article
Language:English
Published: Frontiers Media S.A. 2022-08-01
Series:Frontiers in Bioengineering and Biotechnology
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fbioe.2022.935415/full
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author Chiung Wen Kuo
Feby Wijaya Pratiwi
Yen-Ting Liu
Di-Yen Chueh
Peilin Chen
Peilin Chen
author_facet Chiung Wen Kuo
Feby Wijaya Pratiwi
Yen-Ting Liu
Di-Yen Chueh
Peilin Chen
Peilin Chen
author_sort Chiung Wen Kuo
collection DOAJ
description In the development of bioinspired nanomaterials for therapeutic applications, it is very important to validate the design of nanomaterials in the disease models. Therefore, it is desirable to visualize the change of the cells in the diseased site at the nanoscale. Heart diseases often start with structural, morphological, and functional alterations of cardiomyocyte components at the subcellular level. Here, we developed straightforward technique for long-term real-time intravital imaging of contracting hearts without the need of cardiac pacing and complex post processing images to understand the subcellular structural and dynamic changes in the myocardial infarction model. A two-photon microscope synchronized with electrocardiogram signals was used for long-term in vivo imaging of a contracting heart with subcellular resolution. We found that the structural and dynamic behaviors of organelles in cardiomyocytes closely correlated with heart function. In the myocardial infarction model, sarcomere shortening decreased from ∼15% (healthy) to ∼8% (diseased) as a result of impaired cardiac function, whereas the distances between sarcomeres increased by 100 nm (from 2.11 to 2.21 μm) in the diastolic state. In addition, T-tubule system regularity analysis revealed that T-tubule structures that were initially highly organized underwent significant remodeling. Morphological remodeling and changes in dynamic activity at the subcellular level are essential to maintain heart function after infarction in a heart disease model.
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spelling doaj.art-c994ab9373a945b484532fe37230b3242022-12-22T04:00:59ZengFrontiers Media S.A.Frontiers in Bioengineering and Biotechnology2296-41852022-08-011010.3389/fbioe.2022.935415935415Revealing the nanometric structural changes in myocardial infarction models by time-lapse intravital imagingChiung Wen Kuo0Feby Wijaya Pratiwi1Yen-Ting Liu2Di-Yen Chueh3Peilin Chen4Peilin Chen5Research Center for Applied Science, Academia Sinica, Taipei, TaiwanResearch Center for Applied Science, Academia Sinica, Taipei, TaiwanResearch Center for Applied Science, Academia Sinica, Taipei, TaiwanResearch Center for Applied Science, Academia Sinica, Taipei, TaiwanResearch Center for Applied Science, Academia Sinica, Taipei, TaiwanInstitute of Physics, Academia Sinica, Taipei, TaiwanIn the development of bioinspired nanomaterials for therapeutic applications, it is very important to validate the design of nanomaterials in the disease models. Therefore, it is desirable to visualize the change of the cells in the diseased site at the nanoscale. Heart diseases often start with structural, morphological, and functional alterations of cardiomyocyte components at the subcellular level. Here, we developed straightforward technique for long-term real-time intravital imaging of contracting hearts without the need of cardiac pacing and complex post processing images to understand the subcellular structural and dynamic changes in the myocardial infarction model. A two-photon microscope synchronized with electrocardiogram signals was used for long-term in vivo imaging of a contracting heart with subcellular resolution. We found that the structural and dynamic behaviors of organelles in cardiomyocytes closely correlated with heart function. In the myocardial infarction model, sarcomere shortening decreased from ∼15% (healthy) to ∼8% (diseased) as a result of impaired cardiac function, whereas the distances between sarcomeres increased by 100 nm (from 2.11 to 2.21 μm) in the diastolic state. In addition, T-tubule system regularity analysis revealed that T-tubule structures that were initially highly organized underwent significant remodeling. Morphological remodeling and changes in dynamic activity at the subcellular level are essential to maintain heart function after infarction in a heart disease model.https://www.frontiersin.org/articles/10.3389/fbioe.2022.935415/fullreal-time intravital imagingtwo-photon imagingnanometric structural changesarcomere lengthsarcomere shortening
spellingShingle Chiung Wen Kuo
Feby Wijaya Pratiwi
Yen-Ting Liu
Di-Yen Chueh
Peilin Chen
Peilin Chen
Revealing the nanometric structural changes in myocardial infarction models by time-lapse intravital imaging
Frontiers in Bioengineering and Biotechnology
real-time intravital imaging
two-photon imaging
nanometric structural change
sarcomere length
sarcomere shortening
title Revealing the nanometric structural changes in myocardial infarction models by time-lapse intravital imaging
title_full Revealing the nanometric structural changes in myocardial infarction models by time-lapse intravital imaging
title_fullStr Revealing the nanometric structural changes in myocardial infarction models by time-lapse intravital imaging
title_full_unstemmed Revealing the nanometric structural changes in myocardial infarction models by time-lapse intravital imaging
title_short Revealing the nanometric structural changes in myocardial infarction models by time-lapse intravital imaging
title_sort revealing the nanometric structural changes in myocardial infarction models by time lapse intravital imaging
topic real-time intravital imaging
two-photon imaging
nanometric structural change
sarcomere length
sarcomere shortening
url https://www.frontiersin.org/articles/10.3389/fbioe.2022.935415/full
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