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CD44介导多形核白细胞在透明质酸上的运动。

CD44 mediates polymorphonuclear leukocyte motility on hyaluronan.

作者信息

Aziz Khalil A

机构信息

Regional Department of Immunology, Birmingham Heartlands Hospital, Bordesley Green East, Birmingham, B9 5SS, United Kingdom.

出版信息

Saudi Med J. 2003 Aug;24(8):827-31.

Abstract

OBJECTIVE

To investigate the behavior of polymorphonuclear (PMN) leukocytes on the extracellular matrix carbohydrate component, hyaluronan (HA), in the presence and absence of the chemokine, interleukin-8 (IL-8).

METHODS

The present study was conducted at the Department of Hematology, University of Liverpool, United Kingdom, between the period 2000 to 2001. Polymorphonuclear cells were isolated from whole venous blood using Mono-Poly-Resolving Medium. Purified PMN were added alone or with IL-8 to HA-coated plates and the behavior of these cells monitored by time-lapse video microscopy over a period of 40 minutes. For the identification of surface receptor(s) mediating PMN migration on HA, PMN were incubated with blocking and non-blocking antibodies against cluster of differentiation 44 (CD44) and Receptor for Hyaluronan Mediated Motility (RHAMM) prior to addition to HA-coated surfaces.

RESULTS

Approximately 55% of PMN were found to interact and migrate on HA-coated plates with a mean speed of 6.4 +/- 0.7 mm/min. Addition of IL-8 reduced both the percentage moving cells (7.5%) and the average speed of the remaining moving cells (2.0 +/- 0.3 mm/min). The inhibitory effect of IL-8 on PMN migration was associated with reorganization of the cytoplasmic fibrillar form of actin. Anti-CD44 blocking antibody substantially reduced the speed of PMN (2.5 +/-0.9 mm/min), while non-blocking anti-CD44 and anti-RHAMM antibodies had no effect.

CONCLUSION

The present study demonstrates for the first time that PMN are able to interact and migrate on the widely distributed extracellular matrix component, HA, using the cell surface receptor, CD44. Such interaction is modified by the chemokine, IL-8, in a way that optimizes the host defense against invading pathogens.

摘要

目的

研究在有趋化因子白细胞介素-8(IL-8)和无IL-8的情况下,多形核(PMN)白细胞在细胞外基质碳水化合物成分透明质酸(HA)上的行为。

方法

本研究于2000年至2001年在英国利物浦大学血液学系进行。使用单核-多核分离培养基从全静脉血中分离多形核细胞。将纯化的PMN单独或与IL-8一起添加到HA包被的培养板上,并通过延时视频显微镜在40分钟内监测这些细胞的行为。为了鉴定介导PMN在HA上迁移的表面受体,在将PMN添加到HA包被的表面之前,先用抗分化簇44(CD44)和透明质酸介导运动受体(RHAMM)的封闭和非封闭抗体孵育PMN。

结果

发现约55%的PMN在HA包被的培养板上相互作用并迁移,平均速度为6.4±0.7毫米/分钟。添加IL-8降低了移动细胞的百分比(7.5%)和剩余移动细胞的平均速度(2.0±0.3毫米/分钟)。IL-8对PMN迁移的抑制作用与肌动蛋白细胞质纤维形式的重组有关。抗CD44封闭抗体显著降低了PMN的速度(2.5±0.9毫米/分钟),而非封闭抗CD44和抗RHAMM抗体则没有作用。

结论

本研究首次证明PMN能够利用细胞表面受体CD44在广泛分布的细胞外基质成分HA上相互作用并迁移。这种相互作用被趋化因子IL-8以优化宿主抵御入侵病原体防御的方式所改变。

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