Published January 1, 2024 | Version v1
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Vascular damage and repair - are small-diameter vascular grafts still the "Holy Grail" of tissue engineering?

  • 1. Laboratory of Biomaterials and Tissue Engineering, Institute of Physiology of the Czech Academy of Sciences, Prague, Czech Republic
  • 2. Institut klinicke a experimentalni mediciny

Description

Cardiovascular diseases are the most important cause of morbidity and mortality in the civilized world. Stenosis or occlusion of blood vessels leads not only to events that are directly life-threatening, such as myocardial infarction or stroke, but also to a significant reduction in quality of life, for example in lower limb ischemia as a consequence of metabolic diseases. The first synthetic polymeric vascular replacements were used clinically in the early 1950s. However, they proved to be suitable only for larger-diameter vessels, where the blood flow prevents the attachment of platelets, pro-inflammatory cells and smooth muscle cells on their inner surface, whereas in smaller-diameter grafts (6 mm or less), these phenomena lead to stenosis and failure of the graft. Moreover, these polymeric vascular replacements, like biological grafts (decellularized or devitalized), are cell-free, i.e. there are no reconstructed physiological layers of the blood vessel wall, i.e. an inner layer of endothelial cells to prevent thrombosis, a middle layer of smooth muscle cells to perform the contractile function, and an outer layer to provide innervation and vascularization of the vessel wall. Vascular substitutes with these cellular components can be constructed by tissue engineering methods. However, it has to be admitted that even about 70 years after the first polymeric vascular prostheses were implanted into human patients, there are still no functional small-diameter vascular grafts on the market. The damage to small-diameter blood vessels has to be addressed by endovascular approaches or by autologous vascular substitutes, which leads to some skepticism about the potential of tissue engineering. However, new possibilities of this approach lie in the use of modern technologies such as 3D bioprinting and/or electrospinning in combination with stem cells and prevascularization of tissue-engineered vascular grafts. In this endeavor, sex-related differences in the removal of degradable biomaterials by the cells and in the behavior of stem cells and pre-differentiated vascular cells need to be taken into account.

Notes

This review article, summarizing results from several studies, has been supported by the National Institute for Research of Metabolic and Cardiovascular Diseases project (EXCELES Programme, ID Project No. LX22NPO5104) - funded by the European Union - Next Generation EU. Further support was provided by the Czech Academy of Sciences, Praemium Academiae grant No. AP2202, by the Czech Health Research Council, Ministry of Health of the Czech Republic (grant No. NV19-02-00068), and also by OP JAC Project No. CZ.02.01.01/00/22_008/0004562, of the Ministry of Education, Youth and Sports (MEYS) of the Czech Republic, co-funded by the European Union. We also acknowledge the Light Microscopy Core Facility, Institute of Molecular Genetics, Prague, Czech Republic, supported by MEYS – LM2023050 and RVO – 68378050-KAV-NPUI, for their support with the confocal/widefield/super-resolution imaging/image analysis presented herein. Robin Healey (Czech Technical University in Prague, Czech Republic) is gratefully acknowledged for his language revision of the manuscript.  

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38836460 (PMID)
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0862-8408 (ISSN)
1802-9973 (ISSN)
References
10.33549/physiolres.935294 (DOI)