类器官3D生物打印研究进展。

Medical review (Berlin, Germany) Pub Date : 2025-01-14 eCollection Date: 2025-08-01 DOI:10.1515/mr-2024-0089
Zeqing Li, Long Chen, Jialin Wu, Yikang Chen, Yizhun Zhu, Gang Li, Guoxi Xie, Guosheng Tang, Maobin Xie
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引用次数: 0

摘要

目前用于有效药物筛选的二维(2D)细胞模型由于缺乏生理环境的真实性而受到重大限制。三维类器官模型克服了传统二维细胞模型的局限性,在模拟人体器官的关键功能方面具有巨大的潜力。然而,目前制备三维类器官模型的技术在可重复性、可扩展性和密切复制体内复杂微环境的能力方面存在局限性。此外,传统的3D细胞培养系统通常涉及冗长和劳动密集型的过程,这阻碍了大规模药物筛选所需的高通量应用。3D生物打印技术的进步为这些挑战提供了有希望的解决方案,通过对细胞放置和材料组成进行精确的空间控制,从而促进了比当前技术更生理相关的类器官的创造。本综述全面总结了用于创建类器官模型的3D生物打印技术的最新进展,首先介绍了不同类型的3D生物打印技术(特别是体积生物打印(VBP)技术),然后概述了用于类器官生物打印的生物墨水。此外,我们还介绍了3D生物打印类器官在疾病模型、药物效率评估和再生医学方面的应用。最后,总结了3D生物打印类器官的发展和临床转化所面临的挑战和可能的策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A review of 3D bioprinting for organoids.

Current two-dimensional (2D) cell models for effective drug screening suffer from significant limitations imposed by the lack of realism in the physiological environment. Three-dimensional (3D) organoids models hold immense potential in mimicking the key functions of human organs by overcoming the limitations of traditional 2D cell models. However, current techniques for preparation of 3D organoids models had limitations in reproducibility, scalability, and the ability to closely replicate the complex microenvironment found in vivo. Additionally, traditional 3D cell culture systems often involve lengthy and labor-intensive processes that hinder high-throughput applications necessary for a large-scale drug screening. Advancements in 3D bioprinting technologies offer promising solutions to these challenges by enabling precise spatial control over cell placement and material composition, thereby facilitating the creation of more physiologically relevant organoids than current techniques. This review provides a comprehensive summary of recent advances in 3D bioprinting technologies for creating organoids models, which begins with an introduction to different types of 3D bioprinting techniques (especially focus on volumetric bioprinting (VBP) technique), followed by an overview of bioinks utilized for organoids bioprinting. Moreover, we also introduce the applications of 3D bioprinting organoids in disease models, drug efficiency evaluation and regenerative medicine. Finally, the challenges and possible strategies for the development and clinical translation of 3D bioprinting organoids are concluded.

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