Cartilage Engineering + Regeneration Laboratory, ETHZ, Schafmattstrasse 22, 8093 Zürich, Switzerland.
Osteoarthritis Cartilage. 2013 Dec;21(12):1924-32. doi: 10.1016/j.joca.2013.08.017. Epub 2013 Aug 24.
To determine the in vitro conditions which promote expression of superficial zone protein (SZP).
Chondrocytes from 6-month-old calves were expanded in monolayer culture and the expression of SZP in alginate bead and monolayer culture was quantified with quantitative real time-polymerase chain reaction (qRT-PCR) and immunostaining. The effect of oxygen tension on SZP expression was determined by qRT-PRC analysis of cells cultured in two dimension (2D) and three dimension (3D) under hypoxic (1% pO2) or normoxic (21% pO2) conditions. Finally, to examine the effect of cyclic tensile strain on expression of SZP in 2D and 3D cultures, chondrocytes encapsulated in alginate beams or seeded on type I collagen coated polydimethylsiloxane (PDMS) chambers were subjected to 5% strain at 1 Hz, 2 h/day for 4 days or 2 h at the fourth day of culture and mRNA levels were quantified.
Bovine chondrocytes in monolayer showed a drastic decrease in SZP expression, similar in trend to the commonly reported downregulation of type II collagen (Col2). Chondrocytes embedded in alginate beads for 4 days re-expressed SZP but not Col2. SZP expression was higher under normoxic conditions whereas Col2 was upregulated only in alginate beads under hypoxic conditions. Cyclic mechanical strain showed a tendency to upregulate mRNA levels of SZP.
A microenvironment encompassing a soft encapsulation material and 21% oxygen is sufficient for fibroblastic chondrocytes to re-express SZP. These results serve as a guideline for the design of stratified engineered articular cartilage and suggest that microenvironmental cues (oxygen tension level) strongly influence the pattern of SZP expression in vivo.
确定促进表面区蛋白(SZP)表达的体外条件。
将 6 月龄小牛的软骨细胞在单层培养中扩增,并通过定量实时聚合酶链反应(qRT-PCR)和免疫染色定量测定 SZP 在藻酸盐珠和单层培养中的表达。通过 qRT-PCR 分析在二维(2D)和三维(3D)培养条件下在低氧(1%pO2)或常氧(21%pO2)下培养的细胞,确定氧张力对 SZP 表达的影响。最后,为了研究循环拉伸应变对 2D 和 3D 培养中 SZP 表达的影响,将藻酸盐梁内包封的软骨细胞或接种在 I 型胶原涂覆的聚二甲基硅氧烷(PDMS)室上的软骨细胞在 1Hz、5%应变下施加 2 小时/天,共 4 天,或在培养第 4 天施加 2 小时,并定量测定 mRNA 水平。
单层培养的牛软骨细胞 SZP 表达急剧下降,与通常报道的 II 型胶原(Col2)下调趋势相似。在藻酸盐珠中培养 4 天的软骨细胞重新表达 SZP,但不表达 Col2。在常氧条件下 SZP 表达更高,而在低氧条件下仅在藻酸盐珠中上调 Col2。循环机械应变显示出上调 SZP mRNA 水平的趋势。
包含柔软包封材料和 21%氧气的微环境足以使成纤维样软骨细胞重新表达 SZP。这些结果为分层工程关节软骨的设计提供了指导,并表明微环境线索(氧张力水平)强烈影响体内 SZP 表达模式。