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层层组织微制造支持细胞在体外和体内的增殖。

Layer-by-layer tissue microfabrication supports cell proliferation in vitro and in vivo.

机构信息

Inserm U 1026, Tissue BioEnginnering, Bordeaux Segalen University, Bordeaux, France.

出版信息

Tissue Eng Part C Methods. 2012 Jan;18(1):62-70. doi: 10.1089/ten.TEC.2011.0382. Epub 2011 Nov 7.

Abstract

Layer-by-layer biofabrication represents a novel strategy to create three-dimensional living structures with a controlled internal architecture, using cell micromanipulation technologies. Laser assisted bioprinting (LAB) is an effective printing method for patterning cells, biomolecules, and biomaterials in two dimensions. "Biopapers," made of thin polymer scaffolds, may be appropriate to achieve three-dimensional constructs and to reinforce mechanical properties of printed materials. The aim of this work was to evaluate the effect of the tridimensional organization of cells and biomaterials on cell proliferation in vitro and in vivo. The experimental LAB setup was comprised of an infrared laser, focused onto a glass ribbon coated with an absorbing layer of gold. The cell bioink was made of MG63 cells (50 millions cells/mL in culture medium and 1% alginate), transduced with Luciferase gene for tracking and quantification. The printing substrate was a 100-μm-thick polycaprolacton (PCL) electrospun scaffold. The building sequence comprised sequential layers of cells and PCL scaffolds stacked using two different tridimensional arrangements, which were compared in this study (layer-by-layer vs. seeding on a single locus of the scaffolds). Then the cell-seeded materials were cultured in vitro or implanted in vivo in NOD-SCID mice. The qualitative follow-up involved scanning electron microscopy (SEM) observations, live-dead assays, and histology. The cell amount was quantified by photon imager during 21 days in vitro and 2 months in vivo. Live- dead assay and SEM revealed that the cells survived after printing and spread onto PCL membranes. Circle-shaped patterns were maintained in vitro during the first week but they were no longer observable after 2 weeks, due to cell proliferation. Luciferase tracking displayed that the cell amount was increased in vitro and in vivo when the materials and the cells where stacked layer by layer. Histological sections of the in vivo samples revealed a thicker fibrous tissue in the layer-by-layer samples. We have demonstrated in this study that PCL electrospun biopapers can act as a shock-absorbing mattress for cell printing and could further support cell proliferation. The layer-by-layer printing provided an appropriate 3D environment for cell survival and enhanced cell proliferation in vitro and in vivo.

摘要

逐层生物制造代表了一种使用细胞微操作技术创建具有受控内部结构的三维活体结构的新策略。激光辅助生物打印 (LAB) 是一种有效的二维细胞、生物分子和生物材料打印方法。由薄聚合物支架制成的“生物纸”可能适合于实现三维结构并增强打印材料的机械性能。本工作的目的是评估细胞和生物材料的三维组织对体外和体内细胞增殖的影响。实验性 LAB 设置包括聚焦在涂有金吸收层的玻璃带上的红外激光。细胞生物墨水由转染 Luciferase 基因用于跟踪和定量的 MG63 细胞(5000 万个细胞/mL 的培养基和 1%海藻酸钠)制成。打印基板是 100μm 厚的聚己内酯 (PCL) 电纺支架。构建序列包括使用两种不同的三维排列方式堆叠的细胞和 PCL 支架的顺序层,在本研究中对其进行了比较(逐层与在支架的单个位置上接种种子)。然后将接种细胞的材料在体外培养或植入 NOD-SCID 小鼠体内。定性随访包括扫描电子显微镜 (SEM) 观察、活/死检测和组织学。在体外 21 天和体内 2 个月期间通过光子成像器定量细胞数量。活/死检测和 SEM 表明,细胞在打印后存活并扩散到 PCL 膜上。在体外的第一周内,圆形图案得以保持,但在 2 周后由于细胞增殖而不再可见。Luciferase 跟踪显示,当材料和细胞逐层堆叠时,体外和体内的细胞数量均增加。体内样本的组织学切片显示,层状样品中的纤维组织更厚。本研究表明,PCL 电纺生物纸可以作为细胞打印的减震垫,并进一步支持细胞增殖。逐层打印为细胞存活提供了适当的 3D 环境,并增强了体外和体内的细胞增殖。

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