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利用混沌平流一步法生物打印多通道水凝胶细丝:预血管化类肌肉组织的制造。

One-Step Bioprinting of Multi-Channel Hydrogel Filaments Using Chaotic Advection: Fabrication of Pre-Vascularized Muscle-Like Tissues.

作者信息

Bolívar-Monsalve Edna Johana, Ceballos-González Carlos Fernando, Chávez-Madero Carolina, de la Cruz-Rivas Brenda Guadalupe, Velásquez Marín Silvana, Mora-Godínez Shirley, Reyes-Cortés Luisa María, Khademhosseini Ali, Weiss Paul S, Samandari Mohamadmahdi, Tamayol Ali, Alvarez Mario Moisés, Trujillo-de Santiago Grissel

机构信息

Centro de Biotecnología-FEMSA, Tecnologico de Monterrey, Monterrey, NL, 64849, México.

Departamento de Ingeniería Mecatrónica y Eléctrica, Escuela de Ingeniería y Ciencias, Tecnologico de Monterrey, Monterrey, NL, 64849, México.

出版信息

Adv Healthc Mater. 2022 Dec;11(24):e2200448. doi: 10.1002/adhm.202200448. Epub 2022 Aug 18.

Abstract

The biofabrication of living constructs containing hollow channels is critical for manufacturing thick tissues. However, current technologies are limited in their effectiveness in the fabrication of channels with diameters smaller than hundreds of micrometers. It is demonstrated that the co-extrusion of cell-laden hydrogels and sacrificial materials through printheads containing Kenics static mixing elements enables the continuous and one-step fabrication of thin hydrogel filaments (1 mm in diameter) containing dozens of hollow microchannels with widths as small as a single cell. Pre-vascularized skeletal muscle-like filaments are bioprinted by loading murine myoblasts (C2C12 cells) in gelatin methacryloyl - alginate hydrogels and using hydroxyethyl cellulose as a sacrificial material. Higher viability and metabolic activity are observed in filaments with hollow multi-channels than in solid constructs. The presence of hollow channels promotes the expression of Ki67 (a proliferation biomarker), mitigates the expression of hypoxia-inducible factor 1-alpha , and markedly enhances cell alignment (i.e., 82% of muscle myofibrils aligned (in ±10°) to the main direction of the microchannels after seven days of culture). The emergence of sarcomeric α-actin is verified through immunofluorescence and gene expression. Overall, this work presents an effective and practical tool for the fabrication of pre-vascularized engineered tissues.

摘要

制造含有中空通道的活体结构对于制造厚组织至关重要。然而,目前的技术在制造直径小于数百微米的通道方面效果有限。结果表明,通过含有开式静态混合元件的打印头将载细胞水凝胶和牺牲材料共挤出,能够连续一步制造出含有数十个中空微通道的薄水凝胶细丝(直径1毫米),这些微通道的宽度小至单个细胞。通过将小鼠成肌细胞(C2C12细胞)加载到甲基丙烯酰化明胶-藻酸盐水凝胶中,并使用羟乙基纤维素作为牺牲材料,生物打印出预血管化的骨骼肌样细丝。与实体结构相比,在具有中空多通道的细丝中观察到更高的活力和代谢活性。中空通道的存在促进了Ki67(一种增殖生物标志物)的表达,减轻了缺氧诱导因子1α的表达,并显著增强了细胞排列(即培养7天后,82%的肌肉肌原纤维与微通道的主方向呈±10°排列)。通过免疫荧光和基因表达验证了肌节α-肌动蛋白的出现。总体而言,这项工作为制造预血管化工程组织提供了一种有效且实用的工具。

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