Banerjee A, Parafina J, Bagchi M
Department of Anatomy and Cell Biology, Wayne State University School of Medicine, Detroit, Michigan 48201.
J Cell Biochem. 1992 May;49(1):66-73. doi: 10.1002/jcb.240490112.
Experiments were performed in our laboratory to study the effects of a mammalian 8 kD vitreous humor (VH) factor on the DNA synthesis and mitosis of the epithelial cells of organ cultured rabbit lens. The 8 kD polypeptide factor was purified from mature rabbit vitreous humor by liquid chromatography. Proliferative activities of the epithelial cells of organ cultured lenses were stimulated by 3% rabbit serum. The data from our experiments depicted that the 8 kD VH factor effectively inhibits DNA synthesis and mitosis by the epithelial cells of the organ cultured lens. Our experiments also showed that this 8 kD VH factor can maintain its growth inhibitory activity even when heated for 3 min at 95 degrees C. The growth inhibitory effect of the 8 kD VH factor was dose dependent. Using iodinated vitreal proteins it was demonstrated that the VH proteins are able to enter or bind to lens epithelial cells. The growth inhibitory effect of the 8 kD VH factor was also tested on tissue cultured lens epithelial cells. These experiments showed that the 8 kD VH factor has no growth inhibitory effect on the tissue cultured lens epithelial cells. This experiment has been repeated many times using different concentrations of the factor. These observations suggest that the 8 kD VH factor may have receptors in the lens capsular material (extracellular matrix) and the factor-receptor binding is essential for the growth inhibitory effect.
我们实验室进行了实验,以研究一种哺乳动物8kD玻璃体液(VH)因子对器官培养的兔晶状体上皮细胞DNA合成和有丝分裂的影响。通过液相色谱法从成熟兔玻璃体液中纯化出8kD多肽因子。3%兔血清刺激器官培养晶状体上皮细胞的增殖活性。我们实验的数据表明,8kD VH因子有效抑制器官培养晶状体上皮细胞的DNA合成和有丝分裂。我们的实验还表明,这种8kD VH因子即使在95摄氏度加热3分钟仍能保持其生长抑制活性。8kD VH因子的生长抑制作用呈剂量依赖性。使用碘化玻璃体液蛋白证明,VH蛋白能够进入或结合晶状体上皮细胞。还在组织培养的晶状体上皮细胞上测试了8kD VH因子的生长抑制作用。这些实验表明,8kD VH因子对组织培养的晶状体上皮细胞没有生长抑制作用。使用不同浓度的该因子多次重复了这个实验。这些观察结果表明,8kD VH因子可能在晶状体囊膜物质(细胞外基质)中有受体,并且因子 - 受体结合对于生长抑制作用至关重要。