Condacci I, Cimasoni G, Rey M, Baehni P
Division of Physiopathology and Periodontology, School of Dentistry, Medical Faculty, University of Geneva, Switzerland.
Arch Oral Biol. 1988;33(6):407-12. doi: 10.1016/0003-9969(88)90198-7.
Cells from explants were cultured in the presence of [L-35S]-methionine for 24 h. Cultures containing cycloheximide or cultures frozen immediately after addition of labelled methionine served as controls. The medium was removed and, after washing, cells were disrupted by repeated freezing and thawing. Synthesis of alpha 2-macroglobulin (alpha 2-M) was evaluated by autoradiography of the SDS-PAGE patterns obtained with the culture medium, and by autoradiography of the crossed immunoelectrophoretic patterns obtained with both the cell extract and the culture medium. There was incorporation of labelled methionine in newly-synthesized alpha 2-M. No autoradiographic bands were found in the frozen preparations, and there was a progressive inhibition of globulin synthesis in the presence of increasing concentrations of cycloheximide. This synthesis of alpha 2-M by human gingival fibroblasts may explain the presence of free alpha 2-M in gingival fluid and might be of significance in the control of proteolysis during gingivitis and periodontitis.
将外植体来源的细胞在含有[L-35S]-甲硫氨酸的条件下培养24小时。含有环己酰亚胺的培养物或在添加标记甲硫氨酸后立即冷冻的培养物用作对照。去除培养基,洗涤后,通过反复冻融使细胞裂解。通过对培养基SDS-PAGE图谱的放射自显影以及对细胞提取物和培养基交叉免疫电泳图谱的放射自显影来评估α2-巨球蛋白(α2-M)的合成。新合成的α2-M中有标记甲硫氨酸的掺入。在冷冻制剂中未发现放射自显影条带,并且在环己酰亚胺浓度增加的情况下球蛋白合成受到逐渐抑制。人牙龈成纤维细胞合成α2-M可能解释了龈沟液中游离α2-M的存在,并且可能在牙龈炎和牙周炎期间的蛋白水解控制中具有重要意义。