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一种用于在滑液中培养人关节软骨细胞的三维系统。

A 3D system for culturing human articular chondrocytes in synovial fluid.

作者信息

Brand Joshua A, McAlindon Timothy E, Zeng Li

机构信息

Department of Anatomy and Cellular Biology, Tufts University School of Medicine, USA.

出版信息

J Vis Exp. 2012 Jan 31(59):e3587. doi: 10.3791/3587.

Abstract

Cartilage destruction is a central pathological feature of osteoarthritis, a leading cause of disability in the US. Cartilage in the adult does not regenerate very efficiently in vivo; and as a result, osteoarthritis leads to irreversible cartilage loss and is accompanied by chronic pain and immobility (1,2). Cartilage tissue engineering offers promising potential to regenerate and restore tissue function. This technology typically involves seeding chondrocytes into natural or synthetic scaffolds and culturing the resulting 3D construct in a balanced medium over a period of time with a goal of engineering a biochemically and biomechanically mature tissue that can be transplanted into a defect site in vivo (3-6). Achieving an optimal condition for chondrocyte growth and matrix deposition is essential for the success of cartilage tissue engineering. In the native joint cavity, cartilage at the articular surface of the bone is bathed in synovial fluid. This clear and viscous fluid provides nutrients to the avascular articular cartilage and contains growth factors, cytokines and enzymes that are important for chondrocyte metabolism (7,8). Furthermore, synovial fluid facilitates low-friction movement between cartilaginous surfaces mainly through secreting two key components, hyaluronan and lubricin (9 10). In contrast, tissue engineered cartilage is most often cultured in artificial media. While these media are likely able to provide more defined conditions for studying chondrocyte metabolism, synovial fluid most accurately reflects the natural environment of which articular chondrocytes reside in. Indeed, synovial fluid has the advantage of being easy to obtain and store, and can often be regularly replenished by the body. Several groups have supplemented the culture medium with synovial fluid in growing human, bovine, rabbit and dog chondrocytes, but mostly used only low levels of synovial fluid (below 20%) (11-25). While chicken, horse and human chondrocytes have been cultured in the medium with higher percentage of synovial fluid, these culture systems were two-dimensional (26-28). Here we present our method of culturing human articular chondrocytes in a 3D system with a high percentage of synovial fluid (up to 100%) over a period of 21 days. In doing so, we overcame a major hurdle presented by the high viscosity of the synovial fluid. This system provides the possibility of studying human chondrocytes in synovial fluid in a 3D setting, which can be further combined with two other important factors (oxygen tension and mechanical loading) (29,30) that constitute the natural environment for cartilage to mimic the natural milieu for cartilage growth. Furthermore, This system may also be used for assaying synovial fluid activity on chondrocytes and provide a platform for developing cartilage regeneration technologies and therapeutic options for arthritis.

摘要

软骨破坏是骨关节炎的核心病理特征,骨关节炎是美国导致残疾的主要原因。成人体内的软骨在体内再生效率不高;因此,骨关节炎会导致不可逆的软骨损失,并伴有慢性疼痛和活动障碍(1,2)。软骨组织工程为再生和恢复组织功能提供了广阔的潜力。这项技术通常包括将软骨细胞接种到天然或合成支架中,并在平衡培养基中培养生成的3D构建体一段时间,目标是构建一种生化和生物力学成熟的组织,可移植到体内的缺损部位(3-6)。实现软骨细胞生长和基质沉积的最佳条件对于软骨组织工程的成功至关重要。在天然关节腔中,骨关节表面的软骨浸泡在滑液中。这种清澈且粘稠的液体为无血管的关节软骨提供营养,并含有对软骨细胞代谢很重要的生长因子、细胞因子和酶(7,8)。此外,滑液主要通过分泌两种关键成分透明质酸和润滑素促进软骨表面之间的低摩擦运动(9,10)。相比之下,组织工程软骨最常培养在人工培养基中。虽然这些培养基可能能够为研究软骨细胞代谢提供更明确的条件,但滑液最准确地反映了关节软骨所处的自然环境。事实上,滑液具有易于获取和储存的优点,并且身体通常可以定期补充。几个研究小组在培养人、牛、兔和犬软骨细胞时向培养基中添加了滑液,但大多只使用了低水平的滑液(低于20%)(11-25)。虽然鸡、马和人的软骨细胞已在含有较高百分比滑液的培养基中培养,但这些培养系统是二维的(26-28)。在此,我们展示了我们在3D系统中用高百分比(高达100%)的滑液培养人关节软骨细胞21天的方法。通过这样做,我们克服了滑液高粘度带来的一个主要障碍。该系统提供了在3D环境中研究滑液中人类软骨细胞的可能性,这可以进一步与构成软骨自然环境的另外两个重要因素(氧张力和机械负荷)相结合(29,30),以模拟软骨生长的自然环境。此外,该系统还可用于检测滑液对软骨细胞的活性,并为开发软骨再生技术和关节炎治疗方案提供一个平台。

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本文引用的文献

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Perfusion culture system: Synovial fibroblasts modulate articular chondrocyte matrix synthesis in vitro.
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