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Culture of chondrocytes in alginate surrounded by fibrin gel: characteristics of the cells over a period of eight weeks

机译:在海藻酸盐中被纤维蛋白凝胶包围的软骨细胞培养:八周内细胞的特征

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摘要

OBJECTIVE—To produce tissue engineered cartilage by human articular chondrocytes in vitro for further use in in vivo manipulations for the treatment of cartilage defects.
METHODS—Human articular chondrocytes were cultured in 0.5%, 1.0%, and 2.0% of alginate for up to four weeks. The optimal concentration of an alginate matrix for cell replication and for aggrecan synthesis by chondrocytes was determined. DNA content in the different culture conditions was measured after two and four weeks. Aggrecan synthesis rates and accumulation in the surrounding extracellular matrix were assessed by [35S]sulphate incorporation after the same periods of culture. To follow the outgrowth of chondrocytes from the alginate beads, chondrocytes were cultured for four weeks in 0.5 or 1.0% alginate surrounded by 0.25 or 0.5% fibrin gel. DNA content of each culture was measured after different culture periods. Finally, human chondrocytes in 1.0% alginate beads were embedded in 0.5% fibrin gel for eight weeks. Immunohistochemical analysis for aggrecan, type I and II collagen was performed weekly.
RESULTS—At two weeks the DNA content in each culture significantly increased in 0.5 and 1.0% alginate cultures in comparison with baseline values. This increase continued until week 4 at the three alginate concentrations. Aggrecan synthesis at two weeks was highest in 0.5 and 1.0% alginate cell cultures. At four weeks aggrecan synthesis rates decreased independently of the alginate concentrations. Aggrecan mainly accumulated in the interterritorial matrix. Proliferation of chondrocytes in alginate and outgrowth of these cells in the surrounding fibrin gel were evident throughout the culture period. The accumulation of aggrecan and type II collagen around the cells, in alginate as well as in fibrin gel, gradually increased over the culture period. Type I collagen appeared after six weeks in alginate and in the surrounding fibrin.
CONCLUSION—Human chondrocytes proliferate in this culture system, show an outgrowth into the surrounding fibrin, and synthesise a cartilage-like matrix for up to eight weeks.

机译:目的—由人关节软骨细胞体外生产组织工程软骨,以进一步用于体内操作以治疗软骨缺损。
方法—将人关节软骨细胞分别培养在0.5%,1.0%和2.0%的藻酸盐中长达四个星期。确定了用于细胞复制和软骨细胞聚集蛋白聚糖合成的藻酸盐基质的最佳浓度。两周和四周后测量不同培养条件下的DNA含量。在相同培养时间后,通过[ 35 S]硫酸盐掺入来评估Aggrecan的合成速率和在周围细胞外基质中的积累。为了追踪软骨细胞从藻酸盐珠中的生长,将软骨细胞在0.5%或1.0%藻酸盐中(0.25%或0.5%纤维蛋白凝胶包围)培养四周。在不同的培养期后测量每种培养物的DNA含量。最后,将1.0%藻酸盐珠粒中的人软骨细胞包埋在0.5%纤维蛋白凝胶中八周。每周进行一次聚集蛋白聚糖,I型和II型胶原蛋白的免疫组织化学分析。
结果-在两周时,藻酸盐培养物中0.5%和1.0%的藻酸盐培养物中的DNA含量均比基线值显着增加。在三种藻酸盐浓度下,这种增加一直持续到第4周。在0.5和1.0%的藻酸盐细胞培养物中,两周时Aggrecan的合成最高。在四周时,聚集蛋白聚糖的合成速率下降,而与藻酸盐浓度无关。 Aggrecan主要积累在领土矩阵中。在整个培养期间,藻酸盐中的软骨细胞增殖和周围纤维蛋白凝胶中这些细胞的生长明显。在培养期间,藻酸盐和纤维蛋白凝胶中聚集蛋白聚糖和II型胶原在细胞周围的积累逐渐增加。六周后,藻酸盐和周围的纤维蛋白中出现了I型胶原蛋白。
结论—人类软骨细胞在该培养系统中增殖,向周围的纤维蛋白中长出,并合成软骨样基质长达八周。

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