Lauritzen E, Møller S, Leerhoy J
Acta Pathol Microbiol Immunol Scand C. 1984 Apr;92(2):107-12. doi: 10.1111/j.1699-0463.1984.tb00060.x.
The human leucocyte migration in the leucocyte migration under agarose technique ( LMAT ) was investigated with specific inhibitors of aspartic, sulphhydryl , metallo- and serine proteinases. The general aspartic proteinase inhibitor pepstatin and the highly specific competitive cathepsin D inhibitor, N-gly-glu-gly-phe-leu-gly-D-phe-leu suppressed leucocyte migration at concentrations of 20-200 mumol/l and 30-59 mumol/l, respectively. The suphhydryl enzyme inactivator, N-ethylmaleimide suppressed leucocyte migration at concentrations of 100-200 mumol/l. Several inhibitors of serine- and metallo enzymes were tested, but none had any effect on leucocyte mobility, although the metal binding agent 8-hydroxyquinoline was strongly inhibitory to cell migration, the significance of which is discussed.
采用天冬氨酸、巯基、金属和丝氨酸蛋白酶的特异性抑制剂,研究了琼脂糖技术(LMAT)下的人白细胞迁移。通用天冬氨酸蛋白酶抑制剂胃蛋白酶抑制剂和高特异性竞争性组织蛋白酶D抑制剂N-甘氨酰-谷氨酸-甘氨酸-苯丙氨酸-亮氨酸-甘氨酸-D-苯丙氨酸-亮氨酸分别在20-200μmol/L和30-59μmol/L的浓度下抑制白细胞迁移。巯基酶失活剂N-乙基马来酰亚胺在100-200μmol/L的浓度下抑制白细胞迁移。测试了几种丝氨酸和金属酶抑制剂,但均对白细胞迁移没有任何影响,尽管金属螯合剂8-羟基喹啉对细胞迁移有强烈抑制作用,本文对此的意义进行了讨论。