Injectable pre-cultured tissue modules catalyze the formation of extensive functional microvasculature in vivo
Autor: | Xiaowei Hong, Andrew J. Putnam, Nicole E. Friend, Ana Y. Rioja, Jan P. Stegemann, Cheri X. Deng, Yen Peng Kong, Julia C. Habif, Jeffrey A. Beamish, Jonathan R. Bezenah |
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Jazyk: | angličtina |
Rok vydání: | 2020 |
Předmět: |
0301 basic medicine
Cell Neovascularization Physiologic lcsh:Medicine 02 engineering and technology Fibrin Article Neovascularization Biomaterials Cell delivery Mice 03 medical and health sciences Tissue engineering In vivo Human Umbilical Vein Endothelial Cells medicine Animals Humans Distribution (pharmacology) lcsh:Science Cells Cultured Multidisciplinary Tissue Scaffolds biology Chemistry lcsh:R Hydrogels Fibroblasts 021001 nanoscience & nanotechnology Microspheres In vitro Cell biology 030104 developmental biology medicine.anatomical_structure Cardiovascular diseases Microvessels Self-healing hydrogels Regenerative medicine biology.protein lcsh:Q medicine.symptom 0210 nano-technology |
Zdroj: | Scientific Reports, Vol 10, Iss 1, Pp 1-16 (2020) Scientific Reports |
ISSN: | 2045-2322 |
DOI: | 10.1038/s41598-020-72576-5 |
Popis: | 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. |
Databáze: | OpenAIRE |
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