Laboratory of Biomaterials and Tissue Engineering, Institute of Physiology of the Czech Academy of Sciences, Prague, Czech Republic.
Physiol Res. 2024 May 31;73(Suppl 1):S335-S363. doi: 10.33549/physiolres.935294.
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 pre-vascularization 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. Key words: Blood vessel prosthesis, Regenerative medicine, Stem cells, Footprint-free iPSCs, sr-RNA, Dynamic bioreactor, Sex-related differences.
心血管疾病是文明世界发病率和死亡率的最重要原因。血管狭窄或闭塞不仅会导致直接危及生命的事件,如心肌梗死或中风,还会显著降低生活质量,例如代谢疾病导致的下肢缺血。第一批合成聚合物血管替代品于 20 世纪 50 年代初在临床上使用。然而,它们仅适用于较大直径的血管,在这些血管中,血流阻止血小板、促炎细胞和平滑肌细胞在内表面附着,而在较小直径的移植物(6 毫米或更小)中,这些现象会导致移植物狭窄和失败。此外,这些聚合物血管替代品与生物移植物(去细胞或去活)一样,是无细胞的,即没有重建的血管壁生理层,即防止血栓形成的内层内皮细胞、执行收缩功能的中层平滑肌细胞和提供血管壁神经支配和血管化的外层。具有这些细胞成分的血管替代品可以通过组织工程方法构建。然而,必须承认,即使在第一批聚合物血管假体植入人体患者后约 70 年,市场上仍然没有功能性的小直径血管移植物。小直径血管的损伤必须通过血管内方法或自体血管替代品来解决,这导致人们对组织工程的潜力产生了一些怀疑。然而,这种方法的新可能性在于使用现代技术,如 3D 生物打印和/或静电纺丝与干细胞相结合,并对组织工程血管移植物进行预血管化。在这项努力中,需要考虑细胞对可降解生物材料的去除以及干细胞和预分化血管细胞的行为方面的性别差异。关键词:血管假体、再生医学、干细胞、无足迹 iPSCs、sr-RNA、动态生物反应器、性别差异。