McKay D A, Kusel J R, Wilkinson P C
Department of Immunology, University of Glasgow, Western Infirmary, UK.
J Cell Sci. 1991 Nov;100 ( Pt 3):473-9. doi: 10.1242/jcs.100.3.473.
Differences in membrane composition between the anterior and posterior poles of human blood neutrophils on exposure to chemoattractant were studied using a laser microscope, and the effects of attractant concentration and time on the ability of neutrophils to polarize were determined. The findings were as follows. (1) The fluorescein-labelled chemotactic hexapeptide fLeu-Norleu-Phe-Norleu-Tyr-Lys was asymmetrically distributed on polarized cells with the highest concentration at the anterior pole of the cell. (2) Differences in membrane lipid behaviour were studied by fluorescence recovery after photobleaching (FRAP) using the probe 5-N-(octadecanoyl)-aminofluorescein. Recovery curves suggested that the proportion of mobile lipid probe at the anterior pole of the cell was higher than at the posterior. However, no difference was found in the rate of recovery between the two poles. (3) Studies of the time-course of polarization were undertaken using neutrophils in suspension exposed to different isotropic concentrations of fMet-Leu-Phe (fMLP). At low concentrations (less than or equal to 10(-9) M), the cells polarized immediately on exposure to the attractant. At a high concentration (10(-7) M) they assumed multipolar morphologies and polarized very poorly, suggesting that ligand binding was too rapid for the cells to form a dominant pole. At the optimal concentration, 10(-8) M fMLP, the cells assumed irregular, ruffled, morphologies after 30s, but showed an increasing proportion of polarized forms over the next 30 min.(ABSTRACT TRUNCATED AT 250 WORDS)
利用激光显微镜研究了人类血液中性粒细胞前后极在接触趋化因子时膜成分的差异,并确定了趋化因子浓度和时间对中性粒细胞极化能力的影响。研究结果如下:(1)荧光素标记的趋化六肽fLeu-Norleu-Phe-Norleu-Tyr-Lys在极化细胞上呈不对称分布,细胞前极浓度最高。(2)使用探针5-N-(十八烷酰基)-氨基荧光素通过光漂白后荧光恢复(FRAP)研究膜脂行为差异。恢复曲线表明,细胞前极的可移动脂质探针比例高于后极。然而,两极之间的恢复速率没有差异。(3)使用悬浮在不同各向同性浓度的fMet-Leu-Phe(fMLP)中的中性粒细胞进行极化时间进程研究。在低浓度(小于或等于10^-9 M)下,细胞在接触趋化因子后立即极化。在高浓度(10^-7 M)下,它们呈现多极形态且极化很差,这表明配体结合太快,细胞无法形成主导极。在最佳浓度10^-8 M fMLP下,细胞在30秒后呈现不规则、有褶皱的形态,但在接下来的30分钟内极化形式的比例不断增加。(摘要截短于250字)