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Review
. 2022 Feb 21;9(2):64.
doi: 10.3390/jcdd9020064.

Soft-Tissue Material Properties and Mechanogenetics during Cardiovascular Development

Affiliations
Review

Soft-Tissue Material Properties and Mechanogenetics during Cardiovascular Development

Hummaira Banu Siddiqui et al. J Cardiovasc Dev Dis. .

Abstract

During embryonic development, changes in the cardiovascular microstructure and material properties are essential for an integrated biomechanical understanding. This knowledge also enables realistic predictive computational tools, specifically targeting the formation of congenital heart defects. Material characterization of cardiovascular embryonic tissue at consequent embryonic stages is critical to understand growth, remodeling, and hemodynamic functions. Two biomechanical loading modes, which are wall shear stress and blood pressure, are associated with distinct molecular pathways and govern vascular morphology through microstructural remodeling. Dynamic embryonic tissues have complex signaling networks integrated with mechanical factors such as stress, strain, and stiffness. While the multiscale interplay between the mechanical loading modes and microstructural changes has been studied in animal models, mechanical characterization of early embryonic cardiovascular tissue is challenging due to the miniature sample sizes and active/passive vascular components. Accordingly, this comparative review focuses on the embryonic material characterization of developing cardiovascular systems and attempts to classify it for different species and embryonic timepoints. Key cardiovascular components including the great vessels, ventricles, heart valves, and the umbilical cord arteries are covered. A state-of-the-art review of experimental techniques for embryonic material characterization is provided along with the two novel methods developed to measure the residual and von Mises stress distributions in avian embryonic vessels noninvasively, for the first time in the literature. As attempted in this review, the compilation of embryonic mechanical properties will also contribute to our understanding of the mature cardiovascular system and possibly lead to new microstructural and genetic interventions to correct abnormal development.

Keywords: arterial pressure; cardiac output; cardiovascular development; cardiovascular microstructure; cardiovascular system; chick embryo; congenital heart defects; embryonic development; embryonic heart; heart-valve development; hemodynamics; optical coherence tomography; residual stresses; soft-tissue mechanics; strain energy.

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Conflict of interest statement

The authors declare no conflict of interest.

Figures

Figure 1
Figure 1
The experimental setup used to evaluate material properties in chick embryos at HH16 (vitelline artery) to HH24 (aortic arch, aa) is shown on the right. (A). Stage HH16 chick embryo imaged under a stereomicroscope is also provided. (B). Preliminary optical coherence tomography images of chick ventricle during acoustic forcing (0–20 kHz) performed for noninvasive elastography. A cross-section of the ventricle is displayed. The arrow points to the instantaneous deformation of the soft tissue.
Figure 2
Figure 2
Overall strain trend of embryonic chick ventricles (LV and RV) presented as a percentage, as compiled from multiple literature sources, from HH11 to HH34. Corresponding references are cited in the text and in Table 2. HH: Hamburger-Hamilton stages.
Figure 3
Figure 3
Representative pressure vs. lumen diameter loops of chick embryonic arteries acquired in vivo. (A). The vitelline arteries under loading and unloading conditions over the cardiac cycle. The data were collected for eight embryos (one representative sample shown) at three consequent stages of HH16, HH17.5, and HH19. (B). Right IVth aortic arch loading and unloading data over the cardiac cycle. The data were collected for five embryos (one sample shown) at two consequent stages of HH18 and HH24. Other sample data are available in the Supplementary Materials, and statistics are provided in Table 3. Data were acquired simultaneously using OCT and the servo-null pressure system described in Section 2.2.
Figure 4
Figure 4
Changes in the effective opening angles of chick embryo arteries during early development are plotted. (A). Opening angle for vitelline arteries at stages HH16, HH17.5, and HH19 during loading and unloading conditions. (B). Opening angles for IVth right aortic arch at stages HH18 and HH24. Plots represent typical data collected over 13 chick embryos. Opening angles were calculated in our lab using the methodology presented in [12] using OCT and servo-null pressure data.

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