采用材料切换数字光处理生物3D打印的流体驱动系统人工子宫。

IF 9.6
Soon Hee Kim, Ji Won Heo, Sudarshini Nath, Moon Sik Oh, Sol Kim, Ji Seung Lee, Kyunghee Kim, Ok Joo Lee, Suk Woo Lee, In-Sun Hong, Chan Hum Park
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引用次数: 0

摘要

尽管使用3D生物打印技术复制复杂器官结构的各种尝试,但制造具有集成血管系统的组织工程子宫内膜仍然是该领域的一个重大挑战。在这项研究中,我们通过将甲基丙烯酸缩水甘油酯修饰的GelMA (GelMAGMA)水凝胶前体与子宫内膜干细胞、基质细胞和内皮细胞结合,开发了三种生物墨水,以创建血管化的子宫内膜结构。利用能够多材料打印的一步材料切换DLP 3D生物打印机,我们成功地制造了一个工程子宫内膜结构,其血管通道延伸到功能层和基底层。使用灌注培养系统使培养基在血管网络中循环,促进细胞活化,雌激素治疗进一步验证了该结构的功能。此外,体内皮下植入证明了工程组织的生物相容性。该平台为组织工程子宫内膜植入以及各种血管化可植入组织的研究提供了巨大的潜力。意义声明:本研究旨在开发用于疾病研究和组织植入的血管化组织工程子宫内膜。主要发现包括基于gelmagma的生物墨水的开发,血管化子宫内膜结构的制造,其功能的验证以及生物相容性的证明。该研究结果推进了组织工程和个性化医疗,对子宫内膜疾病研究和血管化组织模型的开发具有重要意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Artificial uterus with fluidics-driven system using material-switching digital light processing 3D bioprinting.

Despite various attempts to replicate complex organ structures using 3D bioprinting technologies, the fabrication of a tissue-engineered endometrium with integrated vasculature remains a significant challenge in the field. In this study, we developed three bioinks by combining glycidyl methacrylate-modified GelMA (GelMAGMA) hydrogel precursor with endometrial stem cells, stromal cells, and endothelial cells to create a vascularized endometrial construct. Utilizing a one-step material-switching DLP 3D bioprinter capable of multi-material printing, we successfully fabricated an engineered endometrial construct with a vascular channel extending through both the functional and basal layers. The use of a perfusion culture system to circulate medium through the vascular network promoted cell activation, and estrogen treatment further validated the functionality of the construct. Additionally, in vivo subcutaneous implantation demonstrated the biocompatibility of the engineered tissue. This platform offers significant potential for tissue-engineered endometrial implants as well as research into various vascularized implantable tissues. STATEMENT OF SIGNIFICANCE: This study aims to develop a vascularized tissue-engineered endometrium for use in disease research and tissue implantation. Key findings include the development of GelMAGMA-based bioinks, fabrication of a vascularized endometrial construct, validation of its functionality, and proof of biocompatibility. The results advance tissue engineering and personalized medicine, with significant implications for endometrial disease studies and vascularized tissue model development.

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