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Biomaterial-driven in situ cardiovascular tissue engineering : a multi-disciplinary perspective

TLDR
The main current challenges for in situ cardiovascular regeneration are pinpointed and further address, namely the achievement of tissue homeostasis, the development of predictive models for long-term performances of the implanted grafts, and the necessity for stratification for successful clinical translation.
Abstract
There is a persistent and growing clinical need for readily-available substitutes for heart valves and small-diameter blood vessels. In situ tissue engineering is emerging as a disruptive new technology, providing ready-to-use biodegradable, cell-free constructs which are designed to induce regeneration upon implantation, directly in the functional site. The induced regenerative process hinges around the host response to the implanted biomaterial and the interplay between immune cells, stem/progenitor cell and tissue cells in the microenvironment provided by the scaffold in the hemodynamic environment. Recapitulating the complex tissue microstructure and function of cardiovascular tissues is a highly challenging target. Therein the scaffold plays an instructive role, providing the microenvironment that attracts and harbors host cells, modulating the inflammatory response, and acting as a temporal roadmap for new tissue to be formed. Moreover, the biomechanical loads imposed by the hemodynamic environment play a pivotal role. Here, we provide a multidisciplinary view on in situ cardiovascular tissue engineering using synthetic scaffolds; starting from the state-of-the art, the principles of the biomaterial-driven host response and wound healing and the cellular players involved, toward the impact of the biomechanical, physical, and biochemical microenvironmental cues that are given by the scaffold design. To conclude, we pinpoint and further address the main current challenges for in situ cardiovascular regeneration, namely the achievement of tissue homeostasis, the development of predictive models for long-term performances of the implanted grafts, and the necessity for stratification for successful clinical translation.

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Next-generation tissue-engineered heart valves with repair, remodelling and regeneration capacity

TL;DR: An unmet clinical need remains for valve replacements with regenerative, remodelling and growth potential, and next-generation tissue-engineered heart valves (TEHVs) are a promising therapeutic option for patients with valvular heart disease.
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Collagen-Based Tissue Engineering Strategies for Vascular Medicine.

TL;DR: The current state of the art about the use of collagen-based strategies, mainly as a coating material for the functionalization of vascular graft luminal surface, as a drug delivery system for the release of pro-endothelialization factors, and as physiologically relevant in vitro vascular models, and the future trend in this field of research will be presented and discussed.
References
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Arterial grafts exhibiting unprecedented cellular infiltration and remodeling in vivo: The role of cells in the vascular wall

TL;DR: It is demonstrated that SIS-Fibrin grafts can be successfully implanted into the arterial circulation of a clinically relevant animal model, improve the understanding of vascular graft remodeling and raise the possibility of engineering mural cell-free arterial grafts.
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The effect of degradable polymer surfaces on co-cultures of monocytes and smooth muscle cells

TL;DR: The results of this study demonstrated that D-PHI performed equally or better to PLGA in terms of the assayed biological parameters, and suggest that co-culturing monocytes with VSMCs may aid in stimulating the attachment ofVSMCs to D- PHI while eliciting the desired functional phenotypes for both monocytes.
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Effect of Cyclic Mechanical Strain on Glycosaminoglycan and Proteoglycan Synthesis by Heart Valve Cells

TL;DR: Results demonstrate that GAG and PG synthesis by VICs is regulated by cyclic stretching conditions, with numerous differences in the strain-dependent retention and secretion of GAGs and PGS within the leaflet and chordal groups.
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In situ vascular regeneration using substance P-immobilised poly(L-lactide-co-ε-caprolactone) scaffolds: stem cell recruitment, angiogenesis, and tissue regeneration.

TL;DR: Electrospun scaffolds for the fabrication of artificial vascular grafts that can be remodelled within a host by endogenous cell recruitment are developed and may have broad applications in regenerative medicine, and the novel scaffolding materials can be used for in situ tissue regeneration of soft tissues.
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Development of Non-Cell Adhesive Vascular Grafts Using Supramolecular Building Blocks

TL;DR: The development of mechanically stable grafts with non-cell adhesive properties via a mix-and-match approach using ureido-pyrimidinone (UPy)-modified supramolecular polymers is reported, providing the first steps toward advanced supramolescular biomaterials for in situ vascular tissue engineering with control over selective cell capturing.
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