[成人关节软骨细胞在胶原蛋白凝胶中2D和3d培养的差异行为]。

M Niethard, U Schneider, R Wallich
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引用次数: 7

摘要

目的:本研究的目的是评估培养条件对单层(2d)或三维(3d)可生物降解的I型胶原基质中增殖的人软骨细胞分化的影响,并考虑软骨细胞特异性标志物。方法:从9例接受膝关节置换术的成年供体(平均年龄72.1岁)中提取关节软骨细胞。将分离的细胞悬浮液在三维胶原凝胶(3d)或单层(2d)中进行分裂和培养。通过实时荧光定量PCR (real-time PCR)测定不同时间I型和II型胶原mRNA的含量、聚集蛋白和黑色素瘤抑制活性(MIA)。结果:2 d传代细胞I型胶原表达在p00 ~ p01期间显著增加(P = 0.009),而II型胶原表达显著降低(P = 0.022)。胶原I在3d培养中无明显变化,而胶原II在2 ~ 4周后表达明显下降(p = 0.001)。结论:从老年患者获得的成人软骨细胞显示胶原II的表达下降,单层(2d)传代增加,在3d培养中下降延迟。因此,我们质疑软骨细胞的去分化可以通过3d培养来阻止或逆转的假设。基于我们的研究结果,我们建议使用新鲜分离的,因此稀疏去分化的软骨细胞进行移植。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Differential behaviour of human adult arthrotic chondrocytes under 2D- and 3D-cultivation set-ups in a collagen I gel].

Aim: The aim of this study was to assess the influence of culture conditions on the differentiation of human chondrocytes expanded in monolayer (2 D) or a three-dimensional (3 D) biodegradable collagen type I matrix, with regard to chondrocyte-specific markers.

Method: Human arthrotic chondrocytes were taken from nine adult donors (average age 72.1 years) undergoing knee replacement. The isolated cell suspensions were split and cultivated either in a 3-dimensional collagen gel (3 D) or in a monolayer (2 D). The amounts of mRNA for collagen I and II, aggrecan and melanoma inhibitory activity (MIA) were quantified by means of real-time PCR at different times.

Results: The 2 D-passaged cells showed a significant increase of collagen I between P 00 and P 01 (p = 0.009), whereas the expression of collagen II decreased significantly (p = 0.022). There was no significant change for collagen I in 3 D-cultivation, whereas the collagen II expression decreased significantly after 2 to 4 weeks (p = 0.001).

Conclusion: Human adult chondrocytes obtained from elderly patients showed a decreased expression of collagen II with increased passaging in the monolayer (2 D). The decrease was delayed in 3 D-cultivation. We thus question the assumption that the dedifferentiation of chondrocytes can be prevented or reversed by 3 D-cultivation. Based on our results, we recommend the use of freshly isolated and therefore sparsely dedifferentiated chondrocytes for transplantation.

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