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关节软骨细胞对垂体成纤维细胞生长因子(FGF)的反应。

Response of articular chondrocytes to pituitary fibroblast growth factor (FGF).

作者信息

Sachs B L, Goldberg V M, Moskowitz R W, Malemud C J

出版信息

J Cell Physiol. 1982 Jul;112(1):51-9. doi: 10.1002/jcp.1041120109.

Abstract

Rabbit chondrocytes from pooled articular joints have been delineated by their time of attachment to culture flasks after initiation of primary monolayer culture, either attached (48-AT) or floating (48-F) after 48 hours. A general population of chondrocytes (attached after 72 hours, 72-AT) was also studied. The growth-promoting activity of pituitary fibroblast growth factor (FGF) and its effect on sulfated-proteoglycan synthesis was studied on each chondrocyte population in secondary monolayer culture. 3H-thymidine incorporation during a 1-hour pulse was stimulated by FGF (100 ng/ml) in each chondrocyte population. The response of AT-72 chondrocytes to FGF required an additional fetal bovine serum supplement, while 48-F cells responded independent of serum. The response of 48-AT chondrocytes to FGF (100 ng/ml) during a 1-hour pulse with 3H-thymidine was increased in low serum (0.5-2.0%) rather than when high serum (8-10%) was present in the culture medium. FGF reduced 35SO4 incorporation into sulfated-proteoglycans in the 48-AT and 48-F chondrocyte populations, but not in the 72-AT population. The reduction in 35SO4 incorporation in the 48-AT and 48-F chondrocytes was not characterized by alterations in the hydrodynamic size of the sulfated-proteoglycans as measured by Sepharose CL-2B chromatography nor by changes in the types of sulfated-glycosaminoglycans produced. These results indicated that FGF produced quantitative rather than qualitative alterations in chondrocyte sulfated-proteoglycan synthesis. The latter appears uncoupled from the growth-promoting activity of FGF on chondrocytes.

摘要

从汇集的关节中获取的兔软骨细胞,在原代单层培养开始后,根据其贴壁时间进行了分类,培养48小时后,要么贴壁(48-AT),要么悬浮(48-F)。还研究了一般的软骨细胞群体(72小时后贴壁,72-AT)。在第二代单层培养中,研究了垂体成纤维细胞生长因子(FGF)的促生长活性及其对硫酸化蛋白聚糖合成的影响。在每个软骨细胞群体中,FGF(100 ng/ml)刺激了1小时脉冲期间的3H-胸腺嘧啶核苷掺入。AT-72软骨细胞对FGF的反应需要额外添加胎牛血清,而48-F细胞的反应则与血清无关。在低血清(0.5-2.0%)中,48-AT软骨细胞在1小时脉冲期间用3H-胸腺嘧啶核苷对FGF(100 ng/ml)的反应增强,而在培养基中存在高血清(8-10%)时则不然。FGF减少了48-AT和48-F软骨细胞群体中35SO4掺入硫酸化蛋白聚糖,但在72-AT群体中没有。通过琼脂糖CL-2B色谱法测量,48-AT和48-F软骨细胞中35SO4掺入的减少并非由硫酸化蛋白聚糖的流体力学大小改变所致,也不是由产生的硫酸化糖胺聚糖类型变化所致。这些结果表明,FGF在软骨细胞硫酸化蛋白聚糖合成中产生的是定量而非定性的改变。后者似乎与FGF对软骨细胞的促生长活性无关。

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