Rise of tissue- and species-specific 3D bioprinting based on decellularized extracellular matrix-derived bioinks and bioresins

Q3 Biochemistry, Genetics and Molecular Biology
Laura Elomaa , Ahed Almalla , Eriselda Keshi , Karl H. Hillebrandt , Igor M. Sauer , Marie Weinhart
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Abstract

Thanks to its natural complexity and functionality, decellularized extracellular matrix (dECM) serves as an excellent foundation for creating highly cell-compatible bioinks and bioresins. This enables the bioprinted cells to thrive in an environment that closely mimics their native ECM composition and offers customizable biomechanical properties. To formulate dECM bioinks and bioresins, one must first pulverize and/or solubilize the dECM into non-crosslinked fragments, which can then be chemically modified as needed. In bioprinting, the solubilized dECM-derived material is typically deposited and/or crosslinked in a layer-by-layer fashion to build 3D hydrogel structures. Since the introduction of the first liver-derived dECM-based bioinks, a wide variety of decellularized tissue have been employed in bioprinting, including kidney, heart, cartilage, and adipose tissue among others. This review aims to summarize the critical steps involved in tissue-derived dECM bioprinting, starting from the decellularization of the ECM to the standardized formulation of bioinks and bioresins, ultimately leading to the reproducible bioprinting of tissue constructs. Notably, this discussion also covers photocrosslinkable dECM bioresins, which are particularly attractive due to their ability to provide precise spatiotemporal control over the gelation in bioprinting. Both in extrusion printing and vat photopolymerization, there is a need for more standardized protocols to fully harness the unique properties of dECM-derived materials. In addition to mammalian tissues, the most recent bioprinting approaches involve the use of microbial extracellular polymeric substances in bioprinting of bacteria. This presents similar challenges as those encountered in mammalian cell printing and represents a fascinating frontier in bioprinting technology.

基于脱细胞细胞外基质衍生的生物墨水和生物树脂的组织和物种特异性3D生物打印的兴起
由于其天然的复杂性和功能性,脱细胞细胞外基质(dECM)是创造高度细胞相容性的生物墨水和生物树脂的良好基础。这使得生物打印的细胞能够在接近模拟其天然ECM组成的环境中茁壮成长,并提供可定制的生物力学特性。为了制备dECM生物墨水和生物树脂,必须首先将dECM粉碎和/或溶解成非交联碎片,然后根据需要对其进行化学修饰。在生物打印中,溶解的decm衍生材料通常以一层接一层的方式沉积和/或交联,以构建3D水凝胶结构。自从第一个肝脏来源的基于decm的生物墨水问世以来,各种各样的脱细胞组织已经被用于生物打印,包括肾脏、心脏、软骨和脂肪组织等。本综述旨在总结组织源性dECM生物打印的关键步骤,从ECM的脱细胞到生物墨水和生物树脂的标准化配方,最终导致组织结构的可复制生物打印。值得注意的是,本讨论还涵盖了光交联的dECM生物树脂,由于它们能够在生物打印中提供对凝胶化的精确时空控制,因此特别有吸引力。无论是挤压印刷还是还原光聚合,都需要更标准化的协议来充分利用decm衍生材料的独特性能。除了哺乳动物组织外,最近的生物打印方法还包括在细菌生物打印中使用微生物细胞外聚合物物质。这提出了与哺乳动物细胞打印遇到的类似挑战,代表了生物打印技术的一个迷人的前沿。
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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CiteScore
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