Center for Biomedical Engineering, School of Engineering, Brown University, Providence, RI, USA.
Center for Biomedical Engineering, School of Engineering, Brown University, Providence, RI, USA.
Acta Biomater. 2018 Mar 15;69:42-62. doi: 10.1016/j.actbio.2018.01.017. Epub 2018 Jan 31.
The field of tissue engineering has turned towards biomimicry to solve the problem of tissue oxygenation and nutrient/waste exchange through the development of vasculature. Induction of angiogenesis and subsequent development of a vascular bed in engineered tissues is actively being pursued through combinations of physical and chemical cues, notably through the presentation of topographies and growth factors. Presenting angiogenic signals in a spatiotemporal fashion is beginning to generate improved vascular networks, which will allow for the creation of large and dense engineered tissues. This review provides a brief background on the cells, mechanisms, and molecules driving vascular development (including angiogenesis), followed by how biomaterials and growth factors can be used to direct vessel formation and maturation. Techniques to accomplish spatiotemporal control of vascularization include incorporation or encapsulation of growth factors, topographical engineering, and 3D bioprinting. The vascularization of engineered tissues and their application in angiogenic therapy in vivo is reviewed herein with an emphasis on the most densely vascularized tissue of the human body - the heart.
Vascularization is vital to wound healing and tissue regeneration, and development of hierarchical networks enables efficient nutrient transfer. In tissue engineering, vascularization is necessary to support physiologically dense engineered tissues, and thus the field seeks to induce vascular formation using biomaterials and chemical signals to provide appropriate, pro-angiogenic signals for cells. This review critically examines the materials and techniques used to generate scaffolds with spatiotemporal cues to direct vascularization in engineered and host tissues in vitro and in vivo. Assessment of the field's progress is intended to inspire vascular applications across all forms of tissue engineering with a specific focus on highlighting the nuances of cardiac tissue engineering for the greater regenerative medicine community.
组织工程领域已转向仿生学,通过开发脉管系统来解决组织氧合和营养/废物交换的问题。通过物理和化学线索的组合,特别是通过呈现形貌和生长因子,积极诱导血管生成并随后在工程组织中发展血管床。以时空方式呈现血管生成信号开始产生改善的血管网络,这将允许创建大而密集的工程组织。本综述简要介绍了驱动血管生成(包括血管生成)的细胞、机制和分子,然后介绍了生物材料和生长因子如何用于指导血管形成和成熟。实现血管化时空控制的技术包括生长因子的掺入或包封、形貌工程和 3D 生物打印。本文综述了工程组织的血管化及其在体内血管生成治疗中的应用,重点是人体最密集血管化的组织 - 心脏。
血管化对伤口愈合和组织再生至关重要,分层网络的发展使营养物质的转移更加高效。在组织工程中,血管化对于支持生理上密集的工程组织是必要的,因此该领域试图使用生物材料和化学信号诱导血管形成,为细胞提供适当的促血管生成信号。本综述批判性地检查了用于生成具有时空线索的支架的材料和技术,以在体外和体内工程组织和宿主组织中指导血管化。评估该领域的进展旨在激发血管应用于所有形式的组织工程,特别强调突出心脏组织工程的细微差别,以造福更大的再生医学社区。