Jamieson J C
Department of Chemistry, University of Manitoba, Winnipeg, Canada.
Life Sci. 1988;43(8):691-7. doi: 10.1016/0024-3205(88)90140-3.
Liver slices from control and 24hr inflamed rats were incubated for up to 20hr with 5mM 1-deoxynojirimycin (DN), an inhibitor of the processing glucosidases. The amounts of albumin and alpha 1-acid glycoprotein (AGP) and the activities of sialyltransferase were determined in liver and medium. The presence of DN significantly inhibited the release of AGP and sialyltransferase. The inhibitory effect of DN was most pronounced with slices from inflamed rats. Secretion of albumin was not inhibited. Incorporation studies with labelled leucine and mannose showed that the inhibitor did not significantly affect protein synthesis, but it did inhibit mannose incorporation into AGP and sialyltransferase. The results show that DN inhibits the secretion of acute phase AGP and sialyltransferase in liver slices and further suggests that sialyltransferase is a glycoprotein.
将来自对照大鼠和炎症持续24小时的大鼠的肝切片与5mM 1-脱氧野尻霉素(DN,一种加工葡萄糖苷酶抑制剂)一起孵育长达20小时。测定肝脏和培养基中白蛋白和α1-酸性糖蛋白(AGP)的含量以及唾液酸转移酶的活性。DN的存在显著抑制了AGP和唾液酸转移酶的释放。DN对炎症大鼠肝切片的抑制作用最为明显。白蛋白的分泌未受抑制。用标记的亮氨酸和甘露糖进行的掺入研究表明,该抑制剂对蛋白质合成没有显著影响,但确实抑制了甘露糖掺入AGP和唾液酸转移酶。结果表明,DN抑制肝切片中急性期AGP和唾液酸转移酶的分泌,并进一步表明唾液酸转移酶是一种糖蛋白。