Laser-assisted bioprinting of targeted cartilaginous spheroids for high density bottom-up tissue engineering.

IF 8.2 2区 医学 Q1 ENGINEERING, BIOMEDICAL
Gabriella Nilsson Hall, Yuchao Fan, Bertrand Viellerobe, Antonio Iazzolino, Andreas Dimopoulos, Claire Poiron, Aude Clapies, Frank P Luyten, Fabien Guillemot, Ioannis Papantoniou
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引用次数: 0

Abstract

Multicellular spheroids such as microtissues and organoids have demonstrated great potential for tissue engineering applications in recent years as these 3D cellular units enable improved cell-cell and cell-matrix interactions. Current bioprinting processes that use multicellular spheroids as building blocks have demonstrated limited control on post printing distribution of cell spheroids or moderate throughput and printing efficiency. In this work, we presented a laser-assisted bioprinting approach able to transfer multicellular spheroids as building blocks for larger tissue structures. Cartilaginous multicellular spheroids formed by human periosteum derived cells (hPDCs) were successfully bioprinted possessing high viability and the capacity to undergo chondrogenic differentiation post printing. Smaller hPDC spheroids with diameters ranging from ∼100 to 150µm were successfully bioprinted through the use of laser-induced forward transfer method (LIFT) however larger spheroids constituted a challenge. For this reason a novel alternative approach was developed termed as laser induced propulsion of mesoscopic objects (LIPMO) whereby we were able to bioprint spheroids of up to 300µm. Moreover, we combined the bioprinting process with computer aided image analysis demonstrating the capacity to 'target and shoot', through automated selection, multiple large spheroids in a single sequence. By taking advantage of target and shoot system, multilayered constructs containing high density cell spheroids were fabricated.

激光辅助生物打印靶向软骨球体,用于高密度自下而上组织工程。
近年来,微组织和有机体等多细胞球体在组织工程应用方面展现出巨大的潜力,因为这些三维细胞单位能够改善细胞-细胞和细胞-基质之间的相互作用。目前使用多细胞球体作为构建模块的生物打印工艺对细胞球体打印后分布的控制有限,或打印量和打印效率一般。在这项工作中,我们提出了一种激光辅助生物打印方法,能够将多细胞球体作为构建更大组织结构的构件进行转移。由人骨膜衍生细胞(hPDCs)形成的软骨多细胞球体成功地进行了生物打印,具有很高的存活率和打印后进行软骨分化的能力。通过使用激光诱导前向转移法(LIFT),直径约为 100-150 微米的较小 hPDC 球体已成功地进行了生物打印,但较大的球体则构成了挑战。因此,我们开发了一种新颖的替代方法,称为激光诱导介观物体推进法(LIPMO),通过这种方法,我们能够生物打印出最大 300 微米的球体。此外,我们还将生物打印过程与计算机辅助图像分析相结合,通过自动选择,展示了在单个序列中 "瞄准并射击 "多个大型球体的能力。利用 "瞄准和射击 "系统的优势,我们制造出了包含高密度细胞球体的多层构建体。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Biofabrication
Biofabrication ENGINEERING, BIOMEDICAL-MATERIALS SCIENCE, BIOMATERIALS
CiteScore
17.40
自引率
3.30%
发文量
118
审稿时长
2 months
期刊介绍: Biofabrication is dedicated to advancing cutting-edge research on the utilization of cells, proteins, biological materials, and biomaterials as fundamental components for the construction of biological systems and/or therapeutic products. Additionally, it proudly serves as the official journal of the International Society for Biofabrication (ISBF).
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