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可注射预培养组织模块在体内催化广泛功能性微血管的形成。

Injectable pre-cultured tissue modules catalyze the formation of extensive functional microvasculature in vivo.

机构信息

Department of Biomedical Engineering, University of Michigan, Ann Arbor, USA.

Division of Nephrology, Department of Internal Medicine, University of Michigan, Ann Arbor, USA.

出版信息

Sci Rep. 2020 Sep 23;10(1):15562. doi: 10.1038/s41598-020-72576-5.

Abstract

Revascularization of ischemic tissues is a major barrier to restoring tissue function in many pathologies. Delivery of pro-angiogenic factors has shown some benefit, but it is difficult to recapitulate the complex set of factors required to form stable vasculature. Cell-based therapies and pre-vascularized tissues have shown promise, but the former require time for vascular assembly in situ while the latter require invasive surgery to implant vascularized scaffolds. Here, we developed cell-laden fibrin microbeads that can be pre-cultured to form primitive vascular networks within the modular structures. These microbeads can be delivered in a minimally invasive manner and form functional microvasculature in vivo. Microbeads containing endothelial cells and stromal fibroblasts were pre-cultured for 3 days in vitro and then injected within a fibrin matrix into subcutaneous pockets on the dorsal flanks of SCID mice. Vessels deployed from these pre-cultured microbeads formed functional connections to host vasculature within 3 days and exhibited extensive, mature vessel coverage after 7 days in vivo. Cellular microbeads showed vascularization potential comparable to bulk cellular hydrogels in this pilot study. Furthermore, our findings highlight some potentially advantageous characteristics of pre-cultured microbeads, such as volume preservation and vascular network distribution, which may be beneficial for treating ischemic diseases.

摘要

缺血组织的再血管化是许多病理情况下恢复组织功能的主要障碍。促血管生成因子的递送显示出一些益处,但很难重现形成稳定血管所需的复杂因素集。基于细胞的治疗和预血管化组织显示出了希望,但前者需要时间进行原位血管组装,而后者需要进行侵入性手术植入血管化支架。在这里,我们开发了细胞负载的纤维蛋白微珠,这些微珠可以在模块结构内预先培养以形成原始血管网络。这些微珠可以以微创的方式递送,并在体内形成功能性微血管。将内皮细胞和基质成纤维细胞包封的微珠在体外预先培养 3 天,然后注入纤维蛋白基质中,注射到 SCID 小鼠背部侧翼的皮下囊中。从这些预培养的微珠中展开的血管在 3 天内与宿主血管形成功能性连接,并在体内 7 天后表现出广泛的成熟血管覆盖。在这项初步研究中,细胞微珠显示出与块状细胞水凝胶相当的血管生成潜力。此外,我们的发现强调了预培养微珠的一些潜在有利特征,例如体积保持和血管网络分布,这可能有益于治疗缺血性疾病。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa71/7511337/fdc7ba935988/41598_2020_72576_Fig1_HTML.jpg

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