Ryo R, Nakeff A, Huang S S, Ginsberg M, Deuel T F
J Cell Biol. 1983 Feb;96(2):515-20. doi: 10.1083/jcb.96.2.515.
The site of synthesis of platelet-specific proteins remains to be established. With the use of short-term megakaryocyte-enriched cultures, direct evidence was obtained to show that megakaryocytes synthesize the platelet-specific protein, platelet factor 4. A megakaryocyte-enriched fraction of rabbit bone marrow for culture was obtained by centrifugal elutriation and cultured with [3H]leucine. Newly synthesized 3H-platelet factor 4 was sought by copurification with added carrier rabbit platelet factor 4, using heparin agarose affinity chromatography and immunoprecipitation with specific goat anti-rabbit platelet factor 4 antisera. SDS PAGE of the washed immunoprecipitates demonstrated a [3H]leucine-containing peak which migrated identically with purified homogeneous rabbit platelet factor 4. A second, slightly larger molecular-weight protein was identified in the gels also, suggesting that rabbit platelet factor 4 may be synthesized as a larger molecular-weight precursor in rabbit megakaryocytes. These results provide direct evidence that the platelet-specific protein, platelet factor 4, is synthesized in rabbit megakaryocytes before it is packaged into alpha-granules for release in circulating platelets.
血小板特异性蛋白的合成部位仍有待确定。通过使用短期富含巨核细胞的培养物,获得了直接证据表明巨核细胞合成血小板特异性蛋白——血小板第4因子。通过离心淘洗获得用于培养的兔骨髓富含巨核细胞的部分,并用[3H]亮氨酸进行培养。使用肝素琼脂糖亲和层析以及用特异性山羊抗兔血小板第4因子抗血清进行免疫沉淀,通过与添加的载体兔血小板第4因子共纯化来寻找新合成的3H-血小板第4因子。洗涤后的免疫沉淀物的SDS-PAGE显示出一个含[3H]亮氨酸的峰,其迁移情况与纯化的纯兔血小板第4因子相同。凝胶中还鉴定出了第二种分子量稍大的蛋白质,这表明兔血小板第4因子可能在兔巨核细胞中作为分子量更大的前体被合成。这些结果提供了直接证据,证明血小板特异性蛋白血小板第4因子在被包装到α-颗粒中以便在循环血小板中释放之前是在兔巨核细胞中合成的。