Galéra P, Vivien D, Pronost S, Bonaventure J, Rédini F, Loyau G, Pujol J P
Laboratoire de Biochimie du Tissu Conjonctif, CHU Côte de Nacre, Caen, France.
J Cell Physiol. 1992 Dec;153(3):596-606. doi: 10.1002/jcp.1041530322.
The effect of transforming growth factor-beta 1 (TGF-beta 1) on collagen biosynthesis was investigated in confluent primary monolayer cultures of rabbit articular chondrocytes (RAC). Exposure to TGF-beta (0.1, 1, and 10 ng/ml) in serum-free medium caused a dose- and time-dependent stimulation of collagen biosynthesis associated with an increase of steady-state levels of procollagen type II mRNA. Elevation of the mRNA steady-state did not result from a stabilization of the transcript, as shown by measure of the mRNA half-life. Electrophoresis (SDS-PAGE) showed that TGF-beta stimulates the synthesis of most collagen isotypes, including type II, without qualitative change in their distribution. Moreover, pulse-chase experiments revealed that TGF-beta did not affect the processing rate of type II procollagen. TGF-beta slightly stimulated the production of prostaglandin E2 (PGE2), which could in turn exert an inhibition on collagen synthesis. However, addition of indomethacin to block prostaglandin synthesis did not further enhance the TGF-beta-induced stimulation of collagen production, suggesting that this mediator was not implicated in the effect. Moreover, TGF-beta increased steady-state levels of procollagen type II, I, and III mRNAs even in the presence of indomethacin. Despite these increased mRNA levels, only the production of type II collagen was significantly augmented, suggesting that type I procollagen mRNA was not fully translated. In addition, the TGF-beta-induced stimulation of collagen synthesis was observed whenever ascorbic acid is added or not in the culture medium. In conclusion, TGF-beta, which is present in great amount in bone and cartilage, can increase the collagen production of cultured RAC and might therefore play a role in the early events of cartilage repair, such as those observed in osteoarthritis.
在兔关节软骨细胞(RAC)汇合的原代单层培养物中研究了转化生长因子-β1(TGF-β1)对胶原蛋白生物合成的影响。在无血清培养基中暴露于TGF-β(0.1、1和10 ng/ml)会导致胶原蛋白生物合成呈剂量和时间依赖性刺激,同时伴有II型前胶原mRNA稳态水平的增加。如通过测量mRNA半衰期所示,mRNA稳态的升高并非由转录本的稳定化导致。电泳(SDS-PAGE)显示TGF-β刺激了包括II型在内的大多数胶原蛋白同型的合成,但其分布没有质的变化。此外,脉冲追踪实验表明TGF-β不影响II型前胶原的加工速率。TGF-β轻微刺激了前列腺素E2(PGE2)的产生,而PGE2反过来又可能对胶原蛋白合成产生抑制作用。然而,添加吲哚美辛以阻断前列腺素合成并没有进一步增强TGF-β诱导的胶原蛋白产生刺激,这表明该介质与该效应无关。此外,即使在存在吲哚美辛的情况下,TGF-β也会增加II型、I型和III型前胶原mRNA的稳态水平。尽管mRNA水平有所增加,但只有II型胶原蛋白的产生显著增加,这表明I型前胶原mRNA没有完全翻译。此外,无论培养基中是否添加抗坏血酸,都观察到了TGF-β诱导的胶原蛋白合成刺激。总之,在骨骼和软骨中大量存在的TGF-β可以增加培养的RAC的胶原蛋白产生,因此可能在软骨修复的早期事件中发挥作用,例如在骨关节炎中观察到的那些事件。