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Leukocyte recruitment in the airways: an intravital microscopic study of rat tracheal microcirculation.

机译:气道中白细胞募集:大鼠气管微循环的活体内显微镜研究。

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摘要

Because of its relative inaccessibility, inflammatory cell extravasation within the airway circulation in vivo has been difficult to investigate in real time. A new method has been established using intravital microscopy in the anesthetized rat to visualize leukocytes in superficial postcapillary venules of the trachea. This technique has been validated using local superfusion of lipopolysaccharide (LPS) and N-formyl-methionyl-leucyl-phenylalanine (FMLP). Basal leukocyte rolling velocity (55.4 +/- 9.3 microm/s) and adhesion (1.4 +/- 0.3 cells/100 microm) were monitored in postcapillary venules (33.9 +/- 1.3 microm diameter). At all time points up to 90 min, these parameters were unaltered in control rats (n = 7). In contrast, vessels exposed to 1 microg/ml of LPS (n = 6) exhibited a 57% reduction in leukocyte rolling velocity and an increase in the number of adherent cells (4.7 +/- 1 cells/100 microm, P < 0.05). Superfusion with 0.1 microM of FMLP (n = 6) also resulted in a 45% reduction in rolling velocity and an increase in adherent cells (4 +/- 0.7 cells/100 microm, P < 0.05). Histological evaluation confirmed local stimulus-induced leukocyte extravasation. These results demonstrate leukocyte recruitment in the airway microvasculature and provide an important new method to study airway inflammation in real time.
机译:由于其相对不可及,因此难以实时调查体内气道循环内的炎性细胞外渗。已经建立了一种使用活体显微镜在麻醉的大鼠中可视化气管浅毛细血管后小静脉中白细胞的新方法。该技术已通过使用脂多糖(LPS)和N-甲酰基-甲硫酰基-亮氨酰-苯丙氨酸(FMLP)的局部超融合进行了验证。在毛细血管后小静脉(直径33.9 +/- 1.3微米)中监测基底白细胞滚动速度(55.4 +/- 9.3微米/秒)和粘附(1.4 +/- 0.3细胞/ 100微米)。在直至90分钟的所有时间点,这些参数在对照组大鼠中均未改变(n = 7)。相反,暴露于1微克/毫升LPS(n = 6)的血管的白细胞滚动速度降低了57%,贴壁细胞数量增加了(4.7 +/- 1个细胞/ 100微米,P <0.05) 。用0.1 microM FMLP(n = 6)进行的超融合也导致滚动速度降低了45%,粘附细胞增加(4 +/- 0.7细胞/ 100微米,P <0.05)。组织学评估证实了局部刺激引起的白细胞外渗。这些结果表明白细胞募集在气道微脉管系统中,并提供了一种重要的新方法来实时研究气道炎症。

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