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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.
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.
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....
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.......
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,<.......
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
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.).
....Name | Company | Catalog Number | Comments |
1% Agarose | |||
Low melting point agarose | Thermo Fisher | 16520050 | |
Deionized water | - | - | |
Chemicals for tissue clearing | |||
5-Amino-1,3,3-trimethylcyclohexanemethylamine, mixture of cis and trans | Sigma-Aldrich | 118184 | |
D.E.R.â„¢ 332 | Sigma-Aldrich | 31185 | |
D.E.R.â„¢ 736 | Sigma-Aldrich | 31191 | |
Dibenzyl ether (DBE) | Sigma-Aldrich | 33630 | |
Dichloromethane (DCM) | Sigma-Aldrich | 270997 | |
Fluorescent beads | Spherotech | FP-0556-2 | |
Hydrogen peroxide (H2O2) | Sigma-Aldrich | 216736 | |
Methanol | Sigma-Aldrich | 439193 | |
Paraformaldehyde (PFA) | Thermo Fisher | 47392 | |
Phosphate Buffered Saline (PBS) | Sigma-Aldrich | 79383 | |
Potassium Chloride (KCl) | Sigma-Aldrich | P3911 | |
Software and algorithms | |||
Amira | Thermo Fisher Scientific | 2021.2 | |
BigStitcher | Hörl et al.22 | ||
Fiji-ImageJ | Schindelin et al.20 | 1.54f | |
HCImage Live | Hamamatsu Photonics | 4.6.1.2 | |
LabVIEW | National Instruments Corporation | 2017 SP1 | |
Key components of the customized light-sheet system | |||
0.63 - 6.3X Zoom body | Olympus | MVX-ZB10Â | |
10X Illumination objective | Nikon | MRH00105 | |
1X detection objective | Olympus | MV PLAPO 1X/0.25Â | |
473nm DPSS Laser | Laserglow Technologies | LRS-0473-PFM-00100-05 | |
532nm DPSS laser | Laserglow Technologies | LRS-0532-PFM-00100-05 | |
589 nm DPSS laser | Laserglow Technologies | LRS-0589-GFF-00100-05 | |
BNC connector | National Instrument | BNC-2110 | |
Cylindrical lens | Thorlabs | ACY254-050-A | |
DC-Motor Controller, 4 axes | Physik Instrumente | C-884.4DC | |
ETL | Optotune | EL-16-40-TC-VIS-5D-1-C | |
ETL Cable | Optotune | CAB-6-300 | |
ETL Lens Driver | Optotune | EL-E-4i | |
Filter | Chroma | ET525/30 | |
Filter | Chroma | ET585-40 | |
Filter | Chroma | ET645-75 | |
Filter wheel | Shutter Instrument | LAMBDA 10-B | |
Motorized translation stage | Physik Instrumente | L-406.20DG10 | |
Motorized translation stage | Physik Instrumente | L-406.40DG10 | |
Motorized translation stage | Physik Instrumente | M-403.4PD | |
NI multifunction I/O | National Instrument | PCIe-6363 | |
sCMOS camera | Hamamatsu | C13440-20CU | |
Stepper motor | Pololu | 1474 | |
Tube lens | Olympus | MVX-TLU |
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