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Method Article
* Wspomniani autorzy wnieśli do projektu równy wkład.
Here, we present a protocol to visualize developing hearts in zebrafish in 4-Dimensions (4-D). 4-D imaging, via light-sheet fluorescence microscopy (LSFM), takes 3-Dimensional (3-D) images over time, to reconstruct developing hearts. We show qualitatively and quantitatively that shear stress activates endocardial Notch signaling during chamber development, which promotes cardiac trabeculation.
The hemodynamic forces experienced by the heart influence cardiac development, especially trabeculation, which forms a network of branching outgrowths from the myocardium. Genetic program defects in the Notch signaling cascade are involved in ventricular defects such as Left Ventricular Non-Compaction Cardiomyopathy or Hypoplastic Left Heart Syndrome. Using this protocol, it can be determined that shear stress driven trabeculation and Notch signaling are related to one another. Using Light-sheet Fluorescence Microscopy, visualization of the developing zebrafish heart was possible. In this manuscript, it was assessed whether hemodynamic forces modulate the initiation of trabeculation via Notch signaling and thus, influence contractile function occurs. For qualitative and quantitative shear stress analysis, 4-D (3-D+time) images were acquired during zebrafish cardiac morphogenesis, and integrated light-sheet fluorescence microscopy with 4-D synchronization captured the ventricular motion. Blood viscosity was reduced via gata1a-morpholino oligonucleotides (MO) micro-injection to decrease shear stress, thereby, down-regulating Notch signaling and attenuating trabeculation. Co-injection of Nrg1 mRNA with gata1a MO rescued Notch-related genes to restore trabeculation. To confirm shear stress driven Notch signaling influences trabeculation, cardiomyocyte contraction was further arrested via tnnt2a-MO to reduce hemodynamic forces, thereby, down-regulating Notch target genes to develop a non-trabeculated myocardium. Finally, corroboration of the expression patterns of shear stress-responsive Notch genes was conducted by subjecting endothelial cells to pulsatile flow. Thus, the 4-D light-sheet microscopy uncovered hemodynamic forces underlying Notch signaling and trabeculation with clinical relevance to non-compaction cardiomyopathy.
Biomechanical forces, such as hemodynamic shear stress, are intimately involved in cardiac morphogenesis. In response to hemodynamic shear forces, myocardial ridges and grooves develop in a wave-like trabecular network in alignment with the direction of the shear stress across the atrioventricular (AV) valve1. Cardiac trabeculation is necessary to increase contractile function and myocardial mass2. Mutations in Notch signaling pathways result in congenital heart defects in humans and other vertebrates3. For example, gata1a4 and tnnt2a5
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The following methods were performed in compliance with UTA and UCLA IACUC protocols. These experimental groups were used with transgenic Tg(cmlc2:gfp), the wea (weak atrium) or clo (cloche) mutants: (a) wild-type (WT) control, (b) gata1a MO, and (c) tnnt2a MO injections (Table 1).
Model | Name | Modified Genes | Phenotype | Reference |
Control.... |
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LSFM was used in this manuscript in order to acquire high-resolution 2-D and 3-D pictures. As seen in Figure 1A and 1B, the illumination lens directs the light sheet at the sample. Because of the thinness of the light sheet, only a single plane is illuminated. The detection lens is positioned perpendicular to the illumination lens and is focused on the illuminated plane (Figure 1B). The light sheet from the illum.......
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In this protocol, we have shown that 4-D imaging can be used to track the development of a trabecular network in response to changes in biomechanical forces. In particular, the shear stress experienced by endothelial cells initiates the Notch signaling cascade, which in turn promotes trabeculation. In this manuscript, we have shown that (1) gata1a MO injection decreased hematopoiesis and therefore it reduced wall shear stress, (2) tnnt2a MO injection inhibited ventricular contractile function to reduce .......
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The authors have nothing to disclose.
The authors would like to express gratitude to William Talbot from Stanford University for providing the Human Nrg1 cDNA and to Deborah Yelon from UCSD for providing the wea mutants. The authors would also like to thank Cynthia Chen for helping with image acquisition. This study was supported by grants NIH HL118650 (to T.K. Hsiai), HL083015 (to T.K. Hsiai), HD069305 (to N.C. Chi and T.K. Hsiai.), HL111437 (to T.K. Hsiai and N.C. Chi), HL129727 (to T.K. Hsiai), T32HL007895 (to ....
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Name | Company | Catalog Number | Comments |
Clontech Hifi PCR pre-mix | Takara | 639298 | PCR mastermix 1.1.1.1, 1.1.1.2, 1.1.1.5, 1.1.2.1, 3.1.4 |
Human Nrg1 cDNA | Gift from William Talbot, Stanford University, Stanford, California, USA | N/A | Used for trabeculation rescue 1.1.1.3, 1.1.1.4, 1.1.2.1 |
CFX Connect™ Real-Time PCR Detection System | Bio-Rad | 1855201 | PCR Machine 1.1.1.5, 1.1.1.6, 1.1.2.2, 1.1.3.2 |
pCS2+ | GE Health | Plasmid used to synthesize mRNA 1.1.2.1, 1.1.2.4, 1.1.2.5 | |
Nucleospin purification kit | Clontech | 740609.25 | DNA Purification 1.1.2.3, 1.1.2.4, 1.1.6.2 |
T4 DNA ligase | Clontech | 2011A | PCR Ligation solution 1.1.2.5 |
Stellar competent cells | Clontech | 636763 | E. coli cells used for transformation 1.1.2.6, 1.1.3.1, 1.1.3.2 |
Lipofectamine 2000 transfection reagent | Life Technologies | 11668027 | Transfection reagent 1.1.4 |
mMessage SP6 kit | Invitrogen | AM1340 | Kit used to synthesize mRNA 1.1.6.3 |
Aurum Total RNA Mini Kit | Bio-Rad | 7326820 | Purifies RNA 1.1.6.4, 3.1.2 |
GeneTools 4.3.8 | GeneTools | N/A | Software for primer design 1.2.1, 3.1.3 |
EPO cDNA | Creative Biogene | CDFH006026 | Increases WSS 1.2.2, 1.2.3, 1.1.7 |
AG1478 | Sigma-Aldrich | T4182 | ErbB inhibitor 1.3.1 |
E3 medium | To grow embryos 1.3.1, 1.3.2, 5.1.5 | ||
DAPT | Sigma-Aldrich | D5942 | γ-secretase inhibitor 1.3.2 |
Agarose | Sigma-Aldrich | A9539 | Used for mounting embryos 2.1.1.1 |
ORCA-Flash4.0 LT Digital CMOS camera | Hamamatsu Photonics | C11440-42U | Used to capture Images 2.1.1.2, 2.1.1.3 |
Amira Software | FEI Software | N/A | Visualized and Analysed images into 3D, and 4D 2.1.5.1.1-2.1.5.2.8 |
Tricaone mesylate | Sigma-Aldrich | 886-86-2 | Used to humanely sedated or sacrifice embryos 3.1.1 |
iScript cDNA Synthesis Kit | Bio-Rad | 1708890 | Synthesizes cDNA 3.1.2 |
Eppendorf 5424 microcentrifuge | Eppendorf | 05-400-005 | Microcentrifuge 4.1.1.3 |
GI254023X | Sigma-Aldrich | 260264-93-5 | ADAM10 inhibitor 4.1.2, 4.1.3 |
Isoprenaline hydrochloride | Sigma-Aldrich | I5627 | Isoproterenol increases WSS 5.1.5 |
MATLAB | Mathworks | N/A | Cardiac mechanics analysis |
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An erratum was issued for: Light-sheet Fluorescence Microscopy to Capture 4-Dimensional Images of the Effects of Modulating Shear Stress on the Developing Zebrafish Heart. Additional author names were added, and an author affiliation was updated.
The author list was updated from:
Victoria Messerschmidt*1, Zachary Bailey*1, Kyung In Baek2, Richard Bryant1, Rongsong Li2, Tzung K. Hsiai2, Juhyun Lee1
to:
Victoria Messerschmidt*1, Zachary Bailey*1, Kyung In Baek2, Yichen Ding2, Jeffrey J. Hsu2, Richard Bryant1, Rongsong Li2, Tzung K. Hsiai2, Juhyun Lee1
The author affiliation for Rongsong Li was updated from:
Department of Medicine (Cardiology) and Bioengineering, UCLA
to:
College of Health Science and Environmental Engineering, Shenzhen Technology University
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