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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.

DOI:10.1002/jcp.1041120109
PMID:7107715
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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引用本文的文献

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Action of fibroblast growth factor-2 on the intervertebral disc.成纤维细胞生长因子-2对椎间盘的作用。
Arthritis Res Ther. 2008;10(2):R48. doi: 10.1186/ar2407. Epub 2008 Apr 24.
2
Basic fibroblast growth factor inhibits the anabolic activity of insulin-like growth factor 1 and osteogenic protein 1 in adult human articular chondrocytes.碱性成纤维细胞生长因子抑制成人关节软骨细胞中胰岛素样生长因子1和成骨蛋白1的合成代谢活性。
Arthritis Rheum. 2005 Dec;52(12):3910-7. doi: 10.1002/art.21472.
3
Sulfated proteoglycan synthesis by confluent cultures of rabbit costal chondrocytes grown in the presence of fibroblast growth factor.
在成纤维细胞生长因子存在的情况下,由汇合培养的兔肋软骨细胞合成硫酸化蛋白聚糖
J Cell Biol. 1985 Feb;100(2):477-85. doi: 10.1083/jcb.100.2.477.