Leven R M, Schick P K, Budzynski A Z
Blood. 1985 Feb;65(2):501-4.
Fibrinogen synthesis was investigated in guinea pig megakaryocytes. Purified megakaryocytes were incubated with 35S-methionine in methionine-free incubation medium for 18 hours. Newly synthesized fibrinogen in megakaryocyte lysates enriched with purified carrier guinea pig fibrinogen was immunoprecipitated with a specific anti-guinea pig fibrinogen antiserum produced in rabbits. Proteins in the immunoprecipitates were analyzed with a 3.5% to 10.0% gradient polyacrylamide slab gel electrophoresis and auto-radiography. Radioactivity was detected in a protein band of 340,000 daltons. In order to verify fibrinogen synthesis, immunoprecipitate was analyzed by two-dimensional slab gel electrophoresis: (1) the first dimension separated unreduced fibrinogen using a 3.5% to 10.0% gradient gel; (2) following reduction by 2-beta-mercaptoethanol, fibrinogen chains were separated in the second dimension using a 10% gel. Alpha, beta, and gamma fibrinogen chains, which represented carrier guinea pig plasma fibrinogen, were visualized by Coomassie brilliant blue. Autoradiography identified the incorporation of radioactivity into the three fibrinogen chains. In control experiments, immunoprecipitates, produced by exposing megakaryocyte lysates to preimmune rabbit serum and goat anti-rabbit IgG, were also analyzed by the two-dimensional gel system. Radioactivity was not detected in sites corresponding to the migration of fibrinogen subunits. The study demonstrates that isolated guinea pig megakaryocytes can synthesize fibrinogen. The electrophoretic mobility of newly synthesized fibrinogen and subunits is similar to that of guinea pig plasma fibrinogen.
在豚鼠巨核细胞中研究了纤维蛋白原的合成。将纯化的巨核细胞在不含蛋氨酸的孵育培养基中与35S-蛋氨酸一起孵育18小时。用富含纯化载体豚鼠纤维蛋白原的巨核细胞裂解物中的新合成纤维蛋白原,用兔产生的特异性抗豚鼠纤维蛋白原抗血清进行免疫沉淀。用3.5%至10.0%的梯度聚丙烯酰胺平板凝胶电泳和放射自显影分析免疫沉淀物中的蛋白质。在一条340,000道尔顿的蛋白带中检测到放射性。为了验证纤维蛋白原的合成,通过二维平板凝胶电泳分析免疫沉淀物:(1) 第一维使用3.5%至10.0%的梯度凝胶分离未还原的纤维蛋白原;(2) 用2-巯基乙醇还原后,在第二维使用10%的凝胶分离纤维蛋白原链。代表载体豚鼠血浆纤维蛋白原的α、β和γ纤维蛋白原链,用考马斯亮蓝染色可见。放射自显影鉴定了放射性掺入到三条纤维蛋白原链中。在对照实验中,也通过二维凝胶系统分析了将巨核细胞裂解物暴露于免疫前兔血清和山羊抗兔IgG产生的免疫沉淀物。在与纤维蛋白原亚基迁移相对应的位点未检测到放射性。该研究表明,分离的豚鼠巨核细胞可以合成纤维蛋白原。新合成的纤维蛋白原及其亚基的电泳迁移率与豚鼠血浆纤维蛋白原相似。