Nelson R D, McCormack R T, Fiegel V D, Simmons R L
Infect Immun. 1978 Nov;22(2):441-4. doi: 10.1128/iai.22.2.441-444.1978.
Human polymorphonuclear neutrophils have been preexposed to activated complement as zymosan-activated serum (ZAS) or to the chemotactic oligopeptide N-formyl methionylphenylalanine (F-Met-Phe). Spontaneous migration and chemotactic responses toward the deactivating and other cytotaxins were monitored after washing and resuspension of cells in cytotaxin-free medium. Two patterns of deactivation were observed. Preexposure of the leukocytes to high doses of ZAS or F-Met-Phe decreased all subsequent migratory responses. Preexposure of the leukocytes to lower doses of ZAS or F-Met-Phe decreased only a subsequent chemotactic response to the deactivating cytotaxin. These results suggest two mechanisms, or components, of chemotactic deactivation.
人类多形核中性粒细胞已预先暴露于经酵母聚糖激活的血清(ZAS)激活的补体或趋化寡肽N-甲酰甲硫氨酰苯丙氨酸(F-Met-Phe)中。在将细胞洗涤并重悬于无趋化因子的培养基后,监测其对失活趋化因子和其他细胞趋化素的自发迁移和趋化反应。观察到两种失活模式。白细胞预先暴露于高剂量的ZAS或F-Met-Phe会降低所有随后的迁移反应。白细胞预先暴露于较低剂量的ZAS或F-Met-Phe只会降低随后对失活趋化因子的趋化反应。这些结果提示了趋化失活的两种机制或成分。