Sasazaki Y, Seedhom B B, Shore R
Division of Bioengineering, Academic Unit of Musculoskeletal Disease, Leeds Dental Institute, University of Leeds, Leeds, UK.
Rheumatology (Oxford). 2008 Nov;47(11):1641-6. doi: 10.1093/rheumatology/ken341. Epub 2008 Sep 16.
We compared the morphology and cytoskeleton of chondrocytes seeded in monolayer or in agarose gels with those retained in situ i.e. within their extracellular matrix-the chondrocyte's natural habitat.
Cartilage specimens were harvested from adult bovine femora. Chondrocytes were either enzymatically isolated to seed in both monolayer and agarose gel culture conditions or retained in situ. Full thickness cartilage on bone was sliced both parallel and perpendicular to the articular surface. After immunostaining, the morphology of chondrocytes and of their cytoskeletal organization, i.e. distribution of actin and vimentin, in chondrocytes seeded both in monolayer and 3D agarose and those retained in situ, were assessed using confocal laser scanning microscopy.
The general cytoskeletal disposition of chondrocytes in situ was similar to that in agarose gel. Actin was seen to form stress fibres only in 2D culture, but not in 3D culture and in situ. In these latter conditions, actin showed a punctate staining pattern. The vimentin meshwork spanned the cytoplasm from the plasma membrane to the nuclear membrane in all culture conditions. However, the organization of the vimentin had a radiate organization in chondrocytes in monolayer and a more circumferential arrangement both in agarose gel and in situ. We further observed: (i) the prevalence of a bichondral configuration of chondrocytes in situ and (ii) the existence of a vimentin link joining some of the sister cells in situ.
Bichondral configuration linked with cytoskeletal elements may potentially be significant for the normal function of the chondrocytes, and therefore have implications for approaches to tissue engineering of cartilage.
我们比较了接种于单层或琼脂糖凝胶中的软骨细胞与原位保留的软骨细胞(即在其细胞外基质——软骨细胞的天然栖息地内)的形态和细胞骨架。
从成年牛股骨采集软骨标本。软骨细胞要么通过酶法分离后接种于单层和琼脂糖凝胶培养条件下,要么原位保留。将骨上的全层软骨切成平行和垂直于关节面的薄片。免疫染色后,使用共聚焦激光扫描显微镜评估单层和三维琼脂糖中接种的软骨细胞以及原位保留的软骨细胞的形态及其细胞骨架组织,即肌动蛋白和波形蛋白的分布。
原位软骨细胞的一般细胞骨架布局与琼脂糖凝胶中的相似。仅在二维培养中观察到肌动蛋白形成应力纤维,而在三维培养和原位中未观察到。在这些后一种条件下,肌动蛋白呈现点状染色模式。在所有培养条件下,波形蛋白网络从质膜延伸至核膜跨越细胞质。然而,波形蛋白的组织在单层软骨细胞中呈辐射状排列,在琼脂糖凝胶和原位中则呈更周向的排列。我们还进一步观察到:(i)原位软骨细胞双软骨构型的普遍性;(ii)原位中连接一些姐妹细胞的波形蛋白连接的存在。
与细胞骨架元件相关的双软骨构型可能对软骨细胞的正常功能具有潜在重要意义,因此对软骨组织工程方法具有启示。