可点击的peg -降冰片烯微凝胶支持悬浮生物打印和微血管组装。

Irene W Zhang, Lucia S Choi, Nicole E Friend, Atticus J McCoy, Firaol S Midekssa, Michael M Hu, Eben Alsberg, Sasha Cai Lesher-Pérez, Jan P Stegemann, Brendon M Baker, Andrew J Putnam
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引用次数: 0

摘要

可灌注和多尺度血管网络的发展仍然是组织工程中最大的挑战之一。因此,有必要创建可定制和方便的方法来生成健壮的血管化结构。在本研究中,制备了二级交联(可点击)聚乙二醇-降冰片烯(PEGNB)微珠,并评估了它们依次支持悬浮液生物打印和微血管自组装的能力,以实现工程分层血管系统的目标。可点击的PEGNB微珠浆液具有适合牺牲生物墨水悬浮生物打印的力学行为,可以在打印后紫外交联成颗粒结构,并且可以承受生物墨水的疏散和随后的图案空洞空间的灌注。内皮细胞和基质细胞共嵌在被堵塞的rgd修饰的PEGNB微球浆液中,微球二次交联成颗粒结构后组装成毛细血管尺度的血管系统,内皮小管在微球之间的间隙形成,并由血管周围基质细胞的联合支持。在UV交联之前,将牺牲生物墨水打印到承载细胞的微珠支撑液中,微血管自组装不受影响。总的来说,这些结果表明,可点击的PEGNB微珠是悬浮打印和微血管培养的通用基板,可能是一种有前途的工程分层血管系统方法的基础。意义声明:在这项研究中,我们利用并结合了微凝胶生物材料、颗粒水凝胶、悬浮液生物打印和血管生物学的进展,创造了相对大体积(约500毫米)的血管化结构。我们制备了二级交联(可点击)聚乙二醇-降冰片烯(PEGNB)微珠,并证明了它们依次支持悬浮液生物打印和微血管自组装的能力,以实现工程分层血管系统的目标。据我们所知,这是第一个使用PEG微凝胶作为生物打印支撑材料的研究,也是第一个记录颗粒结构中微血管自组装的论文之一。将自上而下和自下而上的方法结合在一个单一的结构中代表了一个重要的和创新的贡献,我们相信这将引起生物材料和再生医学界的广泛兴趣。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Clickable PEG-norbornene microgels support suspension bioprinting and microvascular assembly.

The development of perfusable and multiscale vascular networks remains one of the largest challenges in tissue engineering. As such, there is a need for the creation of customizable and facile methods to produce robustly vascularized constructs. In this study, secondarily crosslinkable (clickable) poly(ethylene glycol)-norbornene (PEGNB) microbeads were produced and evaluated for their ability to sequentially support suspension bioprinting and microvascular self-assembly towards the aim of engineering hierarchical vasculature. The clickable PEGNB microbead slurry exhibited mechanical behavior suitable for suspension bioprinting of sacrificial bioinks, could be UV crosslinked into a granular construct post-print, and withstood evacuation of the bioink and subsequent perfusion of the patterned void space. Endothelial and stromal cells co-embedded within jammed RGD-modified PEGNB microbead slurries assembled into capillary-scale vasculature after secondary crosslinking of the beads into granular constructs, with endothelial tubules forming within the interstitial space between microbeads and supported by the perivascular association of the stromal cells. Microvascular self-assembly was not impacted by printing sacrificial bioinks into the cell-laden microbead support bath before UV crosslinking. Collectively, these results demonstrate that clickable PEGNB microbeads are a versatile substrate for both suspension printing and microvascular culture and may be the foundation for a promising methodology to engineer hierarchical vasculature. STATEMENT OF SIGNIFICANCE: In this study, we leveraged and combined advances in microgel biomaterials, granular hydrogels, suspension bioprinting, and vascular biology to create relatively large volume (>500 mm3) vascularized constructs. We fabricated secondarily crosslinkable (clickable) poly(ethylene glycol)-norbornene (PEGNB) microbeads and demonstrated their ability to sequentially support suspension bioprinting and microvascular self-assembly towards the aim of engineering hierarchical vasculature. To the best of our knowledge, this is the first study that uses PEG microgels as supportive materials for bioprinting, and one of the first papers to document microvascular self-assembly within granular constructs. The combination of top-down and bottom-up approaches within a single construct represents a significant and innovative contribution that we believe will be of broad interest to the biomaterials and regenerative medicine communities.

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