2016
DOI: 10.1016/j.drudis.2016.04.017
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Bioengineered vascular constructs as living models for in vitro cardiovascular research

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Cited by 23 publications
(17 citation statements)
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“…In this way, a regenerative, biological implant, which will not be attacked immunologically by the host, is converted successively to truly endogenous tissue in the course of the physiological remodelling. Tubular structures of fibrin and collagen can be constructed in vitro as an alternative to decellularisation of preformed donor tissue [26,72].…”
Section: The Ideal Vascular Prosthesismentioning
confidence: 99%
“…In this way, a regenerative, biological implant, which will not be attacked immunologically by the host, is converted successively to truly endogenous tissue in the course of the physiological remodelling. Tubular structures of fibrin and collagen can be constructed in vitro as an alternative to decellularisation of preformed donor tissue [26,72].…”
Section: The Ideal Vascular Prosthesismentioning
confidence: 99%
“…This vessel can, however, be functionalized with human endothelial cells cultured at the inner wall of the vessel while human perivascular cells (e.g., vascular smooth muscle cells, pericytes, and astrocytes) cultured in the wall surrounding the vessel [ 89 , 90 ]. Following functionalization, this blood vessel can be subjected to biochemical cues (e.g., low-density lipoprotein, high-density lipoprotein, and human whole blood) and mechanical cues (e.g., flow-induced shear stress) to create functional human in vitro atherosclerotic models [ 91 , 92 ]. This biomimetic model would be useful for exploring potential therapeutic effects of hMSCs in atherosclerosis for the prevention of tissue ischemia.…”
Section: Challenges Associated With Future Translation Of Hmscs Tomentioning
confidence: 99%
“…In order to deal with the above-mentioned inter-species and inter-patient variability in the processes of material-driven inflammation and regeneration, the development of dedicated models is paramount. In vitro engineered laboratory models, based on human cells (either healthy or diseased) can be exploited to gain an initial understanding of tissue integration and remodeling in response to scaffolds (e.g., reviewed by 86 and 87 ). Dynamic in vitro co-culture platforms are eminently suitable to screen the interactions between human (circulatory) immune cells and valvular scaffolds under physiologically relevant hemodynamic stimuli, such as shear stress ( 88–90 ) and cyclic strains ( 91, 92 ).…”
Section: Outstanding Challengesmentioning
confidence: 99%