Unanue E R, Kíely J M
J Immunol. 1977 Sep;119(3):925-31.
We have examined the biosynthesis and fate of the mitogenic protein (MP)2 made by macrophages. This mitogenic protein was assayed by its stimulation of DNA synthesis of thymocytes. Macrophages freshly harvested from the peritoneal cavity did not contain MP in the cell. The MP, however, rapidly appeared in the cell, reaching maximum amount by 1 to 2 hr, maintaining its concentration up to about 6 hr, and then disappearing. The disappearance of MP did not correlate with its secretion into the medium. The elaboration of MP stimulated by contact with the dish was inhibited by cycloheximide. Exposure of the cells to inhibitors of protein synthesis after 1 to 2 hr of culture at a time when the MP was already made produced a striking increase in secretion. The MP inside the cell did not appear to decay in the presence of cycloheximide. This result thus represents another example of superinduction. The intracellular fate of MP appears to be under the regulation of a control protein.
我们已经研究了巨噬细胞产生的促有丝分裂蛋白(MP)2的生物合成和去向。这种促有丝分裂蛋白通过其对胸腺细胞DNA合成的刺激作用来测定。刚从腹腔收获的巨噬细胞在细胞内不含MP。然而,MP迅速出现在细胞中,1至2小时达到最大量,其浓度维持至约6小时,然后消失。MP的消失与其分泌到培养基中无关。与培养皿接触刺激产生的MP受环己酰亚胺抑制。在培养1至2小时,MP已经产生时,将细胞暴露于蛋白质合成抑制剂会导致分泌显著增加。在环己酰亚胺存在下,细胞内的MP似乎不会降解。因此,这一结果代表了超诱导的另一个例子。MP在细胞内的去向似乎受一种调控蛋白的调节。