Chopra R, Anastassiades T
Department of Medicine, Queen's University, Kingston, Ontario, Canada.
J Rheumatol. 1998 Aug;25(8):1578-84.
To determine the specificity of and possible synergism among polypeptide growth factors (PGF) on the net synthesis of proteoglycan and a novel high molecular weight anionic glycoprotein (HMW AG), of roughly 540 kDa, by articular chondrocyte cultures.
Confluent articular chondrocyte cultures were labeled with either [35S]SO4 or [3H]glucosamine and [35S]SO4 and stimulated by adding the individual PGF or combinations of the PGF. Alcian blue dye precipitation was used for direct rapid quantification of newly synthesized proteoglycans from the media of the 35S labeled cultures. To assess the effects of the PGF on the synthesis of the HMW AG, a toluidine blue dye batch precipitation method was used for isolation of anionic glycoconjugates from the media of the 3H and 35S labeled articular chondrocyte cultures, followed by chondroitinase ABC digestion and gradient sodium dodecyl sulfate polyacrylamide gel electrophoresis.
Optimal concentrations of transforming growth factor-beta1 (TGF-beta), insulin-like growth factor-1 (IGF), and platelet derived growth factor (PDGF) stimulated net proteoglycan synthesis per cell by 178, 106, and 101%, respectively. In combinations, TGF-beta + PDGF, TGF-beta + IGF, and PDGF + IGF gave stimulations of proteoglycan synthesis of 418, 384, and 217%, respectively. HMW AG net synthesis was induced by all 3 PGF, but the degree of induction was much greater with TGF-beta.
Net proteoglycan synthesis by articular chondrocyte cultures is synergistically stimulated by the addition of optimal concentrations of combinations of TGF-beta + PDGF and TGF-beta + IGF, but not PDGF + IGE Net HMW AG synthesis is preferentially stimulated by TGF-beta.
通过关节软骨细胞培养,确定多肽生长因子(PGF)对蛋白聚糖和一种分子量约为540 kDa的新型高分子量阴离子糖蛋白(HMW AG)净合成的特异性及可能的协同作用。
将汇合的关节软骨细胞培养物用[35S]SO4或[3H]葡萄糖胺及[35S]SO4标记,通过添加单个PGF或PGF组合进行刺激。阿尔新蓝染料沉淀法用于直接快速定量35S标记培养物培养基中新合成的蛋白聚糖。为评估PGF对HMW AG合成的影响,采用甲苯胺蓝染料批量沉淀法从3H和35S标记的关节软骨细胞培养物培养基中分离阴离子糖缀合物,随后进行软骨素酶ABC消化和梯度十二烷基硫酸钠聚丙烯酰胺凝胶电泳。
转化生长因子-β1(TGF-β)、胰岛素样生长因子-1(IGF)和血小板衍生生长因子(PDGF)的最佳浓度分别使每个细胞的蛋白聚糖净合成增加178%、106%和101%。联合使用时,TGF-β + PDGF、TGF-β + IGF和PDGF + IGF分别使蛋白聚糖合成增加418%、384%和217%。所有3种PGF均诱导HMW AG净合成,但TGF-β诱导程度更大。
添加最佳浓度的TGF-β + PDGF和TGF-β + IGF组合可协同刺激关节软骨细胞培养物中的蛋白聚糖净合成,但PDGF + IGF组合不能。TGF-β优先刺激HMW AG净合成。