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转化生长因子β对源自膝关节半月板的细胞和外植体培养物中蛋白聚糖合成的影响。

Effects of transforming growth factor beta on proteoglycan synthesis by cell and explant cultures derived from the knee joint meniscus.

作者信息

Collier S, Ghosh P

机构信息

Raymond Purves Bone and Joint Research Laboratories (University of Sydney), Royal North Shore Hospital of Sydney, St Leonards, NSW, Australia.

出版信息

Osteoarthritis Cartilage. 1995 Jun;3(2):127-38. doi: 10.1016/s1063-4584(05)80045-7.

Abstract

Repair of meniscal tears depends in part upon the ability of the resident fibrochondrocytes to produce new extracellular matrix molecules including proteoglycans. Three culture systems have been used to investigate proteoglycan production by meniscal fibrochondrocytes from the inner, middle and outer zones of medial and lateral menisci of the sheep stifle joint. Cultures of meniscal explants, monolayered cells, and cells encapsulated in alginate beads were labeled with 35SO4H2 for 48 h in the absence and presence of transforming growth factor beta (TGF beta) and the proteoglycans were analysed by Sephacryl S-1000 chromatography. In general, the lateral meniscus produced more proteoglycan than the medial. Explants from the inner and middle zones produced predominantly aggrecan-like proteoglycan, together with a smaller proteoglycan population eluting with an average distribution coefficient of around 0.65. The outer meniscal zones synthesized less proteoglycan overall, the majority of which consisted of the smaller proteoglycans. These characteristic proteoglycan size profiles obtained with explant cultures also were preserved when cells isolated from the respective zones were cultured in alginate beads. Monolayer cell cultures, however, produced almost entirely small proteoglycans, regardless of their zone of origin. Chromatography of chondroitinase AC and ABC digested samples indicated that the small proteoglycan population comprised mostly dermatan sulphate-containing proteoglycans. In all meniscal zones and in all culture systems, TGF beta stimulated proteoglycan production by up to 100% and the proteoglycans were slightly larger. TGF beta also stimulated cell division in fibrochondrocyte monolayer cultures. Long term intermittent stimulation of alginate bead cultures with TGF beta resulted in large increases in proteoglycan synthesis, increased aggregation of large proteoglycan monomers, and an increase in the production of the larger of two small proteoglycans, putatively, biglycan.

摘要

半月板撕裂的修复部分取决于驻留的纤维软骨细胞产生包括蛋白聚糖在内的新细胞外基质分子的能力。已使用三种培养系统来研究绵羊膝关节内侧和外侧半月板内、中、外区的半月板纤维软骨细胞产生蛋白聚糖的情况。在不存在和存在转化生长因子β(TGF-β)的情况下,将半月板外植体、单层细胞和包封在藻酸盐珠中的细胞培养物用35SO4H2标记48小时,并通过Sephacryl S-1000色谱法分析蛋白聚糖。一般来说,外侧半月板产生的蛋白聚糖比内侧半月板多。来自内区和中区的外植体主要产生聚集蛋白聚糖样蛋白聚糖,以及一小部分平均分配系数约为0.65洗脱的较小蛋白聚糖群体。外侧半月板区总体上合成的蛋白聚糖较少,其中大部分由较小的蛋白聚糖组成。当从各个区域分离的细胞在藻酸盐珠中培养时,外植体培养获得的这些特征性蛋白聚糖大小分布也得以保留。然而,单层细胞培养物几乎完全产生小蛋白聚糖,无论其来源区域如何。软骨素酶AC和ABC消化样品的色谱分析表明,小蛋白聚糖群体主要由含硫酸皮肤素的蛋白聚糖组成。在所有半月板区域和所有培养系统中,TGF-β刺激蛋白聚糖的产生高达100%,并且蛋白聚糖略大。TGF-β还刺激纤维软骨细胞单层培养物中的细胞分裂。用TGF-β长期间歇性刺激藻酸盐珠培养物导致蛋白聚糖合成大幅增加、大蛋白聚糖单体聚集增加以及两种小蛋白聚糖中较大的一种(推测为双糖链蛋白聚糖)产量增加。

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