Lee D A, Bentley G, Archer C W
Institute of Orthopaedics (University College and Middlesex School of Medicine, Stanmore, U.K.
Osteoarthritis Cartilage. 1993 Apr;1(2):137-46. doi: 10.1016/s1063-4584(05)80029-9.
Our objective was to investigate the factors that control chondrocyte division, namely, (1) steric hindrance caused by the surrounding matrix, (2) growth factors and (3) cell shape. Bovine articular cartilage explants and isolated chondrocytes were cultured in medium containing [3H]-TdR to measure DNA synthesis. The effect of enzyme treatment, growth factors and cell shape was investigated. Proteoglycan (PG) depletion did not stimulate DNA synthesis whilst disruption of the collagen architecture promoted incorporation of [3H]-TdR into DNA. DNA synthesis was also stimulated by IGF-1 in flattened chondrocytes but not in rounded cells. It was found that the control of chondrocyte division depends on several variably related factors that may act singly or together to induce cell division and that PG depletion alone is insufficient to induce DNA synthesis, but division was noted when PG depletion was accompanied by matrix disruption and cell shape changes. Cell shape appears to alter the chondrocytes ability to respond to IGF-1 as a mitogen.
我们的目标是研究控制软骨细胞分裂的因素,即:(1)周围基质引起的空间位阻,(2)生长因子,以及(3)细胞形状。将牛关节软骨外植体和分离的软骨细胞培养于含有[3H] - 胸腺嘧啶核苷(TdR)的培养基中,以测量DNA合成。研究了酶处理、生长因子和细胞形状的影响。蛋白聚糖(PG)耗竭并未刺激DNA合成,而胶原蛋白结构的破坏则促进了[3H] - TdR掺入DNA。在扁平的软骨细胞中,胰岛素样生长因子-1(IGF-1)也刺激了DNA合成,但在圆形细胞中则不然。研究发现,软骨细胞分裂的控制取决于几个相互关联程度不一的因素,这些因素可能单独或共同作用以诱导细胞分裂,并且单独的PG耗竭不足以诱导DNA合成,但当PG耗竭伴有基质破坏和细胞形状改变时则会出现细胞分裂。细胞形状似乎会改变软骨细胞作为有丝分裂原对IGF-1作出反应的能力。