Suppr超能文献

用于工程化肌骨组织的自组装培养模型。

Self-Assembly Culture Model for Engineering Musculoskeletal Tissues.

机构信息

University of Pennsylvania, Department of Orthopaedic Surgery, McKay Orthopaedic Research Laboratory, Philadelphia, PA, USA.

Mechano-Therapeutics LLC, Philadelphia, PA, USA.

出版信息

Methods Mol Biol. 2023;2598:313-323. doi: 10.1007/978-1-0716-2839-3_22.

Abstract

The goal of a self-assembly tissue engineering is to create functional tissue following a natural cell-driven process that mirrors natural development. This approach to tissue engineering has tremendous potential for the development of reparative strategies to treat musculoskeletal injuries and diseases, especially for articular cartilage which has poor regenerative capacity. Additionally, many bioengineering and culture methods fail to maintain the chondrocyte phenotype and contain the correct matrix composition in the long term. Existing cartilage-engineering approaches have been developed, but many approaches involve complicated culture techniques and require foreign substances and biomaterials as scaffolds. While these scaffold-based approaches have numerous advantages, such as an instant or rapid creation of biomechanical properties, they frequently result in dedifferentiation of cells in part, due to the adherence to foreign scaffold materials. In this chapter, we describe a novel approach of developing a scaffold-less cartilage-like biomaterial, using the simple principle that cells at high density bear a capacity to coalesce when they cannot attach to any culture substrate. We refer to the biomaterial formed as a cartilage tissue equivalent or CTA and have published to describe their characteristics and utility in high-throughput drug screening. The method is described to generate reproducible cartilage analogs using a specialized high-density suspension culture technique using a hydrogel poly-2-hydroxyethyl methacrylate (polyHEMA) coating of a culture dish. We have demonstrated that this approach can rapidly form biomass of chondrocytes that over time becomes very synthetically active producing a cartilage-like extracellular matrix that closely mimics the biochemical and biomechanical characteristics of native articular cartilage. The culture approach can also be used to form CTA from other than articular cartilage-derived chondrocytes as well as mesenchymal stem cells (MSCs) (while differentiating MSCs into chondrocytes). Some of the advantages are phenotype stability, reproducible CTA size, and biomechanical and biochemical characteristics similar to natural cartilage.

摘要

自组装组织工程的目标是创建具有功能的组织,遵循自然细胞驱动的过程,模拟自然发育。这种组织工程方法在开发修复策略以治疗肌肉骨骼损伤和疾病方面具有巨大潜力,特别是对于具有较差再生能力的关节软骨。此外,许多生物工程和培养方法无法长期保持软骨细胞表型并包含正确的基质组成。已经开发出了现有的软骨工程方法,但许多方法涉及复杂的培养技术,并且需要作为支架的外来物质和生物材料。虽然这些基于支架的方法具有许多优点,例如即时或快速创造生物力学特性,但由于对异物支架材料的附着,它们经常导致细胞部分去分化。在本章中,我们描述了一种开发无支架软骨样生物材料的新方法,该方法使用细胞在高密度时无法附着在任何培养基质上时就会融合的简单原理。我们将形成的生物材料称为软骨组织等效物或 CTA,并已发表描述其在高通量药物筛选中的特性和用途。该方法用于使用特殊的高密度悬浮培养技术在培养皿的聚 2-羟乙基甲基丙烯酸酯 (polyHEMA) 水凝胶涂层上生成可重复的软骨类似物。我们已经证明,这种方法可以快速形成软骨细胞的生物量,随着时间的推移,这些细胞会变得非常具有合成活性,产生类似于天然关节软骨的生物化学和生物力学特性的软骨样细胞外基质。该培养方法也可用于从关节软骨来源的软骨细胞以外的细胞以及间充质干细胞 (MSC) 形成 CTA(同时将 MSC 分化为软骨细胞)。一些优点是表型稳定性、可重复的 CTA 大小以及与天然软骨相似的生物力学和生物化学特性。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验