UGC de Reumatología, Hospital Clínico San Carlos, IdISSC, 28040 Madrid, Spain.
UGC de Traumatología y Cirugía Ortopédica, Hospital Clínico San Carlos, IdISSC, 28040 Madrid, Spain.
Int J Mol Sci. 2024 Sep 11;25(18):9834. doi: 10.3390/ijms25189834.
The existing in vitro and in vivo models for studying osteoarthritis have significant limitations in replicating the complexity of joint tissues. This research aims to validate a Tissue-On-a-Chip system for osteoarthritis research. Osteochondral tissues obtained from knee replacement surgeries of patients with osteoarthritis were cultured in an Organ-On-a-Chip system. This system was designed to supply oxygen and glucose to the cartilage from the bone. The distribution of oxygen and glucose was evaluated by fluorescence using Image-iT Green Hypoxia and 2-NBDG, respectively. Cytotoxicity was measured using lactate dehydrogenase (LDH) levels in chip cultures compared to plate cultures (12 tissues per method). Glycosaminoglycans (GAGs), alkaline phosphatase (ALP), Coll2-1, and procollagen type II N-terminal propeptide (PIINP) were measured in the perfused medium of the Tissue-On-a-Chip over a period of 70 days. Fluorescence of Image-iT Green Hypoxia was observed only in the cartilage area, while 2-NBDG was distributed throughout the tissue. An increase in LDH levels was noted in the plate cultures on day 24 and in the Tissue-On-a-Chip cultures on day 63. Compared to the start of the culture, GAG content increased on day 52, while ALP showed variations. A notable increase in GAG, ALP, and Coll2-1 levels was observed on day 59. PIINP levels remained stable throughout the experiment. The validated osteochondral Tissue-On-a-Chip system can replicate the joint microenvironment, with hypoxic conditions in cartilage and normoxic conditions in bone. Tissue survival and component stability were maintained for approximately two months. This platform is a useful tool for evaluating new drugs and represents a viable alternative to animal models.
用于研究骨关节炎的现有体外和体内模型在复制关节组织的复杂性方面存在显著局限性。本研究旨在验证用于骨关节炎研究的组织芯片系统。从骨关节炎患者膝关节置换手术中获得的骨软骨组织在器官芯片系统中进行培养。该系统旨在从骨骼向软骨提供氧气和葡萄糖。使用 Image-iT Green Hypoxia 和 2-NBDG 分别通过荧光评估氧气和葡萄糖的分布。通过芯片培养物与平板培养物(每种方法 12 个组织)中的乳酸脱氢酶 (LDH) 水平测量细胞毒性。在 70 天的时间内,在组织芯片的灌注培养基中测量糖胺聚糖 (GAG)、碱性磷酸酶 (ALP)、Coll2-1 和原胶原蛋白 II N 端前肽 (PIINP)。仅在软骨区域观察到 Image-iT Green Hypoxia 的荧光,而 2-NBDG 分布在整个组织中。平板培养物中的 LDH 水平在第 24 天增加,而组织芯片培养物中的 LDH 水平在第 63 天增加。与培养开始时相比,GAG 含量在第 52 天增加,而 ALP 显示出变化。在第 59 天观察到 GAG、ALP 和 Coll2-1 水平的显著增加。PIINP 水平在整个实验过程中保持稳定。验证的骨软骨组织芯片系统可以复制关节微环境,软骨中存在缺氧条件,骨骼中存在正常氧条件。组织存活和成分稳定性维持约两个月。该平台是评估新药的有用工具,代表了替代动物模型的可行选择。