Moses A C, Nissley S P, Short P A, Rechler M M, White R M, Knight A B, Higa O Z
Proc Natl Acad Sci U S A. 1980 Jun;77(6):3649-53. doi: 10.1073/pnas.77.6.3649.
Multiplication-stimulating activity (MSA), purified from medium conditioned by the BRL-3A rat liver cell line, previously has been shown to be closely related to the human somatomedins or insulin-like growth factors. A radioimmunoassay was utilized to measure MSA levels in sera from fetal, maternal, and young rats. A serum somatomedin-binding protein was found to interfere in the radioimmunoassay by competing with antibody for binding 125I-labeled MSA. Therefore, prior to radioimmunoassay, sera were filtered on Sephadex G-75 in 1 M acetic acid to dissociate and separate somatomedin activity from the binding protein. Concentrations of MSA by radioimmunoassay were 20- to 100-fold higher in feta rat sera (1.8-4.4 micrograms/ml) than in maternal sera. MSA levels gradually decreased after birth, reaching maternal levels by day 25 of extrauterine life. MSA concentrations in feta rat sera also were found to be correspondingly high by a rat liver membrane radioreceptor assay and a competitive binding protein assay using rat serum somatomedin-binding protein. The findings of higher levels of MSA in fetal than in maternal rat sera and the gradual decline in MSA serum concentrations after birth are in direct contrast to total somatomedin activities measured by biosassay. Thus, MSA may function as a growth factor in the fetal rat whereas other somatomedins may play a role in stimulating growth during extrauterine life.
从BRL - 3A大鼠肝细胞系条件培养基中纯化得到的增殖刺激活性物质(MSA),先前已被证明与人生长调节素或胰岛素样生长因子密切相关。采用放射免疫分析法测定胎儿、母体和幼鼠血清中的MSA水平。发现一种血清生长调节素结合蛋白会与抗体竞争结合125I标记的MSA,从而干扰放射免疫分析。因此,在进行放射免疫分析之前,将血清在1M乙酸中通过葡聚糖凝胶G - 75过滤,以使生长调节素活性与结合蛋白解离并分离。通过放射免疫分析测定,胎儿大鼠血清中MSA的浓度(1.8 - 4.4微克/毫升)比母体血清高20至100倍。出生后MSA水平逐渐下降,在出生后第25天达到母体水平。通过大鼠肝细胞膜放射受体分析和使用大鼠血清生长调节素结合蛋白的竞争性结合蛋白分析,发现胎儿大鼠血清中MSA的浓度也相应较高。胎儿大鼠血清中MSA水平高于母体血清,且出生后MSA血清浓度逐渐下降,这一发现与生物分析测定的总生长调节素活性形成直接对比。因此,MSA可能在胎儿大鼠中作为一种生长因子发挥作用,而其他生长调节素可能在宫外生活期间刺激生长中发挥作用。