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This protocol describes the biaxial mechanical characterization, polarized spatial frequency domain imaging-based collagen quantification, and microdissection of tricuspid valve leaflets. The provided method elucidates how the leaflet layers contribute to the holistic leaflet behaviors.
The tricuspid valve (TV) regulates the unidirectional flow of unoxygenated blood from the right atrium to the right ventricle. The TV consists of three leaflets, each with unique mechanical behaviors. These variations among the three TV leaflets can be further understood by examining their four anatomical layers, which are the atrialis (A), spongiosa (S), fibrosa (F), and ventricularis (V). While these layers are present in all three TV leaflets, there are differences in their thicknesses and microstructural constituents that further influence their respective mechanical behaviors.
This protocol includes four steps to elucidate the layer-specific differences: (i) characterize the mechanical and collagen fiber architectural behaviors of the intact TV leaflet, (ii) separate the composite layers (A/S and F/V) of the TV leaflet, (iii) carry out the same characterizations for the composite layers, and (iv) perform post-hoc histology assessment. This experimental framework uniquely allows the direct comparison of the intact TV tissue to each of its composite layers. As a result, detailed information regarding the microstructure and biomechanical function of the TV leaflets can be collected with this protocol. Such information can potentially be used to develop TV computational models that seek to provide guidance for the clinical treatment of TV disease.
The TV is located between the right atrium and right ventricle of the heart. Throughout the cardiac cycle, the TV regulates the unidirectional blood flow via cyclic opening and closing of the TV anterior leaflet (TVAL), the TV posterior leaflet (TVPL), and the TV septal leaflet (TVSL). These leaflets are complex and have four distinct anatomical layers—the atrialis (A), the spongiosa (S), the fibrosa (F), and the ventricularis (V)—with unique microstructural constituents. The elastin fibers in the atrialis and ventricularis help restore the tissue to its undeformed geometry after mechanical loading1. In contrast, the fibrosa contain....
All methods described herein were approved by the Institutional Animal Care and Use Committee at the University of Oklahoma. Animal tissues were acquired from a USDA-approved slaughterhouse.
1. Biaxial mechanical characterization
The microdissection will yield A/S and F/V specimens with relatively uniform thicknesses that can be mounted to a (commercial) biaxial testing device. Histology analysis of the intact leaflet and the two dissected layers will verify if the tissue was correctly separated along the border between the spongiosa and fibrosa (Figure 7). Additionally, the histology micrographs can be used to determine the tissue layer thicknesses and constituent mass fractions using ImageJ software. A failed disse.......
Critical steps for the protocol include: (i) the layer microdissection, (ii) the tissue mounting, (iii) the fiducial marker placement, and (iv) the pSFDI setup. Appropriate layer microdissection is the most important and difficult aspect of the method described herein. Prior to launching an investigation utilizing this technique, the dissector(s) should have long-term practice with the microdissection technique and all three TV leaflets. The dissector should ensure the composite layer specimens are sufficiently large (&#.......
This work was supported by the American Heart Association Scientist Development Grant (16SDG27760143) and the Presbyterian Health Foundation. KMC was supported in part by the University of Oklahoma (OU) Undergraduate Research Opportunity Program and Honors Research Apprenticeship Program. DWL was supported in part by the National Science Foundation Graduate Research Fellowship (GRF 2019254233) and the American Heart Association/Children's Heart Foundation Predoctoral Fellowship (Award #821298). All of this support is gratefully acknowledged.
....Name | Company | Catalog Number | Comments |
10% Formalin Solution, Neutral Buffered | Sigma-Aldrich | HT501128-4L | |
Alconox Detergent | Alconox | cleaning compound | |
BioTester - Biaxial Tester | CellScale Biomaterials Testing | 1.5 N Load Cell Capacity | |
Cutting Mat | Dahle | B0027RS8DU | |
Deionized Water | N/A | ||
Fine-Tipped Tool | HTI INSTRUMENTS | NSPLS-12 | |
Forceps - Curved | Scientific Labwares | 16122 | |
Forceps - Thick | Scientific Labwares | 161001078 | |
Forceps - Thin | Scientific Labwares | 16127 | |
LabJoy | CellScale Biomaterials Testing | Version 10.66 | |
Laser Displacement Sensor | Keyence | IL-030 | |
Liquid Cyanoacrylate Glue | Loctite | 2436365 | |
MATLAB | MathWorks | Version 2020a | |
Micro Scissors | HTI Instruments | CAS55C | |
Pipette | Belmaks | 360758081051Y4 | |
Polarized Spatial Frequency Domain Imaging Device | N/A | Made in-house using a digital light projector, linear polarizer, rotating polarizer mount, and charge-coupled device camera. See doi.org/10.1016/j.actbio.2019.11.028 (PMCID: PMC8101699) for more details. | |
Scalpel | THINKPRICE | TP-SCALPEL-3010 | |
Single Edge Industrial Razor Blades (Surgical Carbon Steel) | VWR International | H3515541105024 | |
Surgical Pen | LabAider | LAB-Skin-6 | |
T-Pins | Business Source | BSN32351 | |
Wax Board | N/A | Made in-house using modeling wax and baking tray | |
Weigh Boat | Pure Ponta | mdo-azoc-1030 |
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