通过组织工程血管移植物的血管生成,形成层次分明的血管和可硬化组织结构。

Hazem Alkazemi, Geraldine M Mitchell, Zerina Lokmic-Tomkins, Daniel E Heath, Andrea J O'Connor
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引用次数: 0

摘要

临床应用工程组织的主要障碍在于其有限的血管化。植入人体后,这些组织不能尽快与宿主的血液循环融合,通常会导致丧失存活能力和功能。本研究提出了一种解决血管化问题的方法,可使大型、可移植和血管化的工程组织存活并发挥作用。该技术可通过血管生成技术使细胞水凝胶血管化,该血管生成技术由带有大孔的电纺聚己内酯构建而成,可缝合组织工程血管移植物(TEVG)。移植物周围有一层含有细胞的明胶-甲基丙烯酰水凝胶。这种构建物可以缝合,并具有与原生血管相同的机械特性。血管通过移植物上的孔隙生成,从而形成含有广泛血管网络的水凝胶,并与植入式 TEVG 相连。将多个 TEVG 添加到单个构建体中,可增加工程组织的大小和血管化程度。工程组织有可能在与宿主血管手术吻合后立即得到患者血液的灌注,从而使植入细胞得以存活。这些发现为解决制造可缝合的预血管化组织这一长期存在的问题迈出了有意义的一步,这种组织可在体内植入后存活。意义说明:制造可移植并能迅速被宿主血液灌注的血管化工程组织是一项重大挑战,它限制了组织工程的临床影响。在这项研究中,我们展示了一种通过可缝合组织工程血管移植物的血管生成来制造血管化组织结构的技术。大孔移植物周围有水凝胶,使内皮细胞从管腔移出,并通过与大血管相连的毛细血管样结构使水凝胶层血管化。移植物的机械性能与原生血管相当,而且可以通过整合多个移植物来制造更大的构造。这些构建体有可能通过手术与植入部位的血液循环相连接,以支持其即时灌注和存活。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Hierarchically Vascularized and Suturable Tissue Constructs created through Angiogenesis from Tissue-Engineered Vascular Grafts.

A major roadblock in implementing engineered tissues clinically lies in their limited vascularization. After implantation, such tissues do not integrate with the host's circulation as quickly as needed, commonly resulting in loss of viability and functionality. This study presents a solution to the vascularization problem that could enable the survival and function of large, transplantable, and vascularized engineered tissues. The technique allows vascularization of a cell laden hydrogel through angiogenesis from a suturable tissue-engineered vascular graft (TEVG) constructed from electrospun polycaprolactone with macropores. The graft is surrounded by a layer of cell-laden gelatin-methacryloyl hydrogel. The constructs are suturable and possess mechanical properties like native vessels. Angiogenesis occurs through the pores in the graft, resulting in a hydrogel containing an extensive vascular network that is connected to an implantable TEVG. The size of the engineered tissue and the degree of vascularization can be increased by adding multiple TEVGs into a single construct. The engineered tissue has the potential to be immediately perfused by the patient's blood upon surgical anastomosis to host vessels, enabling survival of implanted cells. These findings provide a meaningful step to address the longstanding problem of fabricating suturable pre-vascularized tissues which could survive upon implantation in vivo. STATEMENT OF SIGNIFICANCE: Creating vascularized engineered tissues that can be transplanted and rapidly perfused by the host blood supply is a major challenge which has limited the clinical impact of tissue engineering. In this study we demonstrate a technique to fabricate vascularized tissue constructs via angiogenesis from a suturable tissue-engineered vascular graft. The macroporous graft is surrounded with hydrogel, allowing endothelial cells to migrate from the lumen and vascularize the hydrogel layer with capillary-like structures connected to the macrovessel. The graft has comparable mechanical properties to native blood vessels and larger constructs can be fabricated by incorporating multiple grafts. These constructs could potentially be connected surgically to the circulation at an implantation site to support their immediate perfusion and survival.

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