Díaz-Gil J J, Sánchez G, Santamaría L, Trilla C, Esteban P, Escartín P
Hepatology. 1986 Jul-Aug;6(4):658-61. doi: 10.1002/hep.1840060419.
A liver DNA synthesis promoter activity was detected in human plasma from subjects with hepatitis. The assay procedure consisted of intraperitoneal injection into mice of aliquots of plasma, previously chromatographed on Sephadex G-25. After 24 hr, [3H]thymidine was injected and its incorporation into liver DNA measured. The increase in [3H]thymidine uptake of injected mice was not detected in those administered plasma from normal subjects (basal [3H]thymidine incorporation was that corresponding to saline-injected mouse values). At a maximal effective dose (0.3 mg protein per mouse), plasma from subjects with hepatitis increased the mitotic index of mouse liver hepatocytes; at the same dose, plasma from normal subjects had no effect. This DNA synthesis promoter activity appears to be a protein, as it is sensitive to trypsin digestion and heat.
在患有肝炎的受试者的人血浆中检测到肝脏DNA合成促进活性。检测程序包括将先前在Sephadex G - 25上进行色谱分离的血浆等分试样腹腔注射到小鼠体内。24小时后,注射[3H]胸苷并测量其掺入肝脏DNA的量。在给予正常受试者血浆的小鼠中未检测到注射小鼠的[3H]胸苷摄取增加(基础[3H]胸苷掺入量与注射生理盐水的小鼠值相对应)。在最大有效剂量(每只小鼠0.3毫克蛋白质)下,肝炎患者的血浆增加了小鼠肝脏肝细胞的有丝分裂指数;在相同剂量下,正常受试者的血浆没有作用。这种DNA合成促进活性似乎是一种蛋白质,因为它对胰蛋白酶消化和加热敏感。