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首页> 外文期刊>Osteoarthritis and cartilage >Redifferentiation of dedifferentiated bovine articular chondrocytes in alginate culture under low oxygen tension.
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Redifferentiation of dedifferentiated bovine articular chondrocytes in alginate culture under low oxygen tension.

机译:低氧压力下藻酸盐培养物中去分化的牛关节软骨细胞的再分化。

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摘要

OBJECTIVE: To determine the influence of low oxygen tension on the redifferentiation and matrix production of dedifferentiated articular chondrocytes in monolayer and alginate bead culture. METHODS: Bovine articular chondrocytes were isolated enzymatically. After multiplication and dedifferentiation in a 2-week monolayer culture under 21% oxygen, the cells were subcultured in monolayer or alginate bead culture and subjected to 21% or 5% O(2)for 2 or 3 weeks in order to redifferentiate. Controls consisted of primary cultures in alginate. Matrix production was monitored immunocytochemically [collagen types I, II, IX, and GAGs (keratan sulfate, chondroitin-4- and -6-sulfate)] and collagen type II additionally assayed by Western blotting. Biosynthetic activity was measured by [(3)H]-proline incorporation and cell-viability by the trypan blue exclusion method. RESULTS: The cell number increased more than four-fold during dedifferentiation. Collagen type II was not produced by dedifferentiated chondrocytes under 5% or 21% oxygen in the monolayers or under 21% in alginate. However, dedifferentiated cells in alginate subjected to 5% oxygen exhibited a strong collagen type II expression indicating a redifferentiation. Additionally, collagen type IX and GAGs were also higher and [(3)H]-proline incorporation increased significantly. Primary cultures in alginate displayed a stronger collagen type II expression under 5% but no significant differences for other extracellular matrix components, or [(3)H]-proline incorporation. Viability was approximately 90% for all alginate cultures. CONCLUSION: A combination of alginate and high oxygen tension might not be suitable for redifferentiation or culturing of dedifferentiated chondrocytes. However, low oxygen tension promotes or induces a redifferentiation of dedifferentiated cells in alginate, stimulates their biosynthetic activity, and increases collagen type II production in primary alginate cultures. Copyright 2002 OsteoArthritis Research Society International.
机译:目的:确定低氧张力对单层藻酸盐培养物中去分化的关节软骨细胞再分化和基质产生的影响。方法:酶法分离牛关节软骨细胞。在21%的氧气下于2周的单层培养中进行增殖和去分化后,将细胞在单层或藻酸盐珠培养物中进行亚培养,并使其接受21%或5%O(2)的培养2或3周,以便重新分化。对照包括藻酸盐中的原代培养物。通过免疫细胞化学[I型,II型,IX型和GAG胶原蛋白(硫酸角蛋白,硫酸软骨素4和-6-硫酸盐)]监测基质产生,并通过Western印迹法检测II型胶原。通过[(3)H]-脯氨酸掺入测量生物合成活性,并通过台盼蓝排除法测量细胞活力。结果:去分化过程中细胞数量增加了四倍以上。 II型胶原蛋白不是由去分化的软骨细胞在5%或21%的单层氧气中或21%的藻酸盐中产生的。然而,藻酸盐中的去分化细胞在受到5%氧气的作用下表现出强烈的II型胶原表达,这表明细胞已经发生了再分化。此外,IX型胶原蛋白和GAGs也更高,[(3)H]-脯氨酸的掺入也显着增加。在5%的藻酸盐中,原代培养物显示了较强的II型胶原蛋白表达,但对于其他细胞外基质成分或[(3)H]-脯氨酸掺入没有显着差异。所有藻酸盐培养物的生存力约为90%。结论:藻酸盐和高氧张力的组合可能不适合去分化或去分化软骨细胞的培养。然而,低氧张力促进或诱导藻酸盐中去分化细胞的再分化,刺激它们的生物合成活性,并增加初级藻酸盐培养物中II型胶原的产生。版权所有2002 OsteoArthritis Research Society International。

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