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In This Article

  • Summary
  • Abstract
  • Introduction
  • Protocol
  • Representative Results
  • Discussion
  • Acknowledgements
  • Materials
  • References
  • Reprints and Permissions

Summary

The protocol utilizes advanced light-sheet microscopy along with adapted tissue clearing methods to investigate intricate cardiac structures in rodent hearts, holding great potential for the understanding of cardiac morphogenesis and remodeling.

Abstract

Light-sheet microscopy (LSM) plays a pivotal role in comprehending the intricate three-dimensional (3D) structure of the heart, providing crucial insights into fundamental cardiac physiology and pathologic responses. We hereby delve into the development and implementation of the LSM technique to elucidate the micro-architecture of the heart in mouse models. The methodology integrates a customized LSM system with tissue clearing techniques, mitigating light scattering within cardiac tissues for volumetric imaging. The combination of conventional LSM with image stitching and multiview deconvolution approaches allows for the capture of the entire heart. To address the inherent trade-off between axial resolution and field of view (FOV), we further introduce an axially swept light-sheet microscopy (ASLM) method to minimize out-of-focus light and uniformly illuminate the heart across the propagation direction. In the meanwhile, tissue clearing methods such as iDISCO enhance light penetration, facilitating the visualization of deep structures and ensuring a comprehensive examination of the myocardium throughout the entire heart. The combination of the proposed LSM and tissue clearing methods presents a promising platform for researchers in resolving cardiac structures in rodent hearts, holding great potential for the understanding of cardiac morphogenesis and remodeling.

Introduction

Heart failure remains the leading cause of mortality worldwide, primarily due to the lack of regenerative capacity of mature cardiomyocytes1. The intricate architecture of the heart plays a crucial role in its function and provides insights into developmental processes. A profound understanding of cardiac structure is essential for elucidating the fundamental processes of cardiac morphogenesis and remodeling in response to myocardial infarction. Recent progress has demonstrated that neonatal mice can restore cardiac function following injury, while adult mice lack such regenerative capacity2. This establishes a foundatio....

Protocol

Animal protocols and experiments have been approved and conducted under the oversight of the University of Texas at Dallas Institutional Animal Care and Use Committee (IACUC #21-03). C57BL6 mice, including neonates at postnatal day 1 (P1) and 8-week-old adults, were used in this study. No difference was observed between males and females. All data acquisition and image post-processing were carried out using open-source software or platforms with research or educational licenses. The resources are available from the autho.......

Representative Results

LSM has been demonstrated to foster cardiac studies31,32,33,34,35,36,37 due to the minimal risk of photo damage, high spatial resolution, and optical sectioning as opposed to other optical imaging methods such as brightfield and point-scanning techniques6,<.......

Discussion

The advancement of imaging, computation, and tissue clearing methods has provided an unparalleled opportunity to extensively investigate cardiac structure and function. This holds great potential for deepening our understanding of cardiac morphogenesis and pathogenesis using an intact rodent heart model. In contrast to in vivo studies of zebrafish heart using a similar approach40,41,42,43

Acknowledgements

We express our gratitude to Dr. Eric Olson's group at UT Southwestern Medical Center for generously sharing the animal models. We appreciate all the constructive comments provided by D-incubator members at UT Dallas. This work was supported by NIH R00HL148493 (Y.D.), R01HL162635 (Y.D.), and UT Dallas STARS program (Y.D.).

....

Materials

NameCompanyCatalog NumberComments
1% Agarose
Low melting point agaroseThermo Fisher16520050
Deionized water--
Chemicals for tissue clearing 
5-Amino-1,3,3-trimethylcyclohexanemethylamine, mixture of cis and transSigma-Aldrich118184
D.E.R.â„¢ 332Sigma-Aldrich31185
D.E.R.â„¢ 736Sigma-Aldrich31191
Dibenzyl ether (DBE)Sigma-Aldrich33630
Dichloromethane (DCM)Sigma-Aldrich270997
Fluorescent beadsSpherotechFP-0556-2
Hydrogen peroxide (H2O2)Sigma-Aldrich216736
MethanolSigma-Aldrich439193
Paraformaldehyde (PFA)Thermo Fisher47392
Phosphate Buffered Saline (PBS)Sigma-Aldrich79383
Potassium Chloride (KCl)Sigma-AldrichP3911
Software and algorithms
AmiraThermo Fisher Scientific2021.2
BigStitcherHörl et al.22
Fiji-ImageJSchindelin et al.201.54f
HCImage LiveHamamatsu Photonics4.6.1.2
LabVIEWNational Instruments Corporation2017 SP1
Key components of the customized light-sheet system
0.63 - 6.3X Zoom bodyOlympusMVX-ZB10 
10X Illumination objectiveNikonMRH00105
1X detection objectiveOlympusMV PLAPO 1X/0.25 
473nm DPSS LaserLaserglow TechnologiesLRS-0473-PFM-00100-05
532nm DPSS laserLaserglow TechnologiesLRS-0532-PFM-00100-05
589 nm DPSS laserLaserglow TechnologiesLRS-0589-GFF-00100-05
BNC connectorNational InstrumentBNC-2110
Cylindrical lensThorlabsACY254-050-A
DC-Motor Controller, 4 axesPhysik InstrumenteC-884.4DC
ETLOptotuneEL-16-40-TC-VIS-5D-1-C
ETL CableOptotuneCAB-6-300
ETL Lens DriverOptotuneEL-E-4i
FilterChromaET525/30
FilterChromaET585-40
FilterChromaET645-75
Filter wheel Shutter InstrumentLAMBDA 10-B
Motorized translation stagePhysik InstrumenteL-406.20DG10
Motorized translation stagePhysik InstrumenteL-406.40DG10
Motorized translation stagePhysik InstrumenteM-403.4PD
NI multifunction I/ONational InstrumentPCIe-6363
sCMOS cameraHamamatsuC13440-20CU
Stepper motorPololu1474
Tube lensOlympusMVX-TLU

References

  1. Sadek, H., Olson, E. N. Toward the goal of human heart regeneration. Cell Stem Cell. 26, 7-16 (2020).
  2. Porrello, E. R., et al. Transient regenerative potential of the neonatal mouse heart. Science. 331,....

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