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新生和成年牛中性粒细胞在体外的跨内皮迁移

Transendothelial migration of neonatal and adult bovine neutrophils in vitro.

作者信息

Bochsler P N, Neilsen N R, Slauson D O

机构信息

Department of Pathobiology, College of Veterinary Medicine, University of Tennessee, Knoxville.

出版信息

J Leukoc Biol. 1994 Jan;55(1):43-9. doi: 10.1002/jlb.55.1.43.

Abstract

We have compared and quantitated transendothelial migration of neonatal neutrophils (N-PMNs) and adult bovine peripheral-blood PMNs (A-PMNs) in vitro using monolayers of endothelium and a two-chamber apparatus. Bovine aortic endothelial cells were cultured to confluence on polycarbonate filters perforated with 3.0-micron-diameter pores. 51Cr-labeled PMNs were added to the upper chamber, with or without an anti-CD18 antibody (monoclonal antibody 60.3). Chemotactic stimuli in the lower chambers included recombinant human interleukin-8 (rhIL-8; 75 ng/ml), rhC5a (10(-7) M), and zymosan-activated bovine serum (ZAS; 10%). At 60 min incubation with rhIL-8, greater numbers (P < .01) of N-PMNs (24.70 +/- 5.95%) than of A-PMNs (15.77 +/- 3.66%) had migrated across the endothelial barrier, and a similar difference was present at 90 min. Migration rates of N-PMNs and A-PMNs were similar (P > .05) at all time points when using rhC5a and ZAS as stimuli. Anti-CD18 monoclonal antibody significantly decreased migration (P < .01) of both N-PMNs and A-PMNs to low levels when IL-8 and ZAS were used as stimuli. Because leukocyte integrin expression on PMNs affects transendothelial migration, we also compared surface expression of CD18, CD11a, and CD11c on PMNs from the two age groups. We found no significant quantitative differences in integrin expression between PMNs from the two age groups, regardless of whether the PMNs were incubated with buffer alone or with chemotaxins (rhIL-8, rhC5a, ZAS).

摘要

我们使用内皮细胞单层和双室装置在体外比较并定量了新生中性粒细胞(N-PMNs)和成年牛外周血中性粒细胞(A-PMNs)的跨内皮迁移。将牛主动脉内皮细胞培养至汇合于孔径为3.0微米的聚碳酸酯滤膜上。将51Cr标记的中性粒细胞添加到上室,添加或不添加抗CD18抗体(单克隆抗体60.3)。下室中的趋化刺激物包括重组人白细胞介素-8(rhIL-8;75 ng/ml)、rhC5a(10(-7) M)和酵母聚糖激活的牛血清(ZAS;10%)。与rhIL-8孵育60分钟时,迁移穿过内皮屏障的N-PMNs数量(24.70 +/- 5.95%)多于A-PMNs(15.77 +/- 3.66%)(P <.01),90分钟时也存在类似差异。当使用rhC5a和ZAS作为刺激物时,N-PMNs和A-PMNs在所有时间点的迁移率相似(P >.05)。当使用IL-8和ZAS作为刺激物时,抗CD18单克隆抗体显著降低了N-PMNs和A-PMNs的迁移率(P <.01)至低水平。由于中性粒细胞上白细胞整合素的表达影响跨内皮迁移,我们还比较了两个年龄组中性粒细胞上CD18、CD11a和CD11c的表面表达。我们发现,无论中性粒细胞是单独与缓冲液孵育还是与趋化因子(rhIL-8、rhC5a、ZAS)孵育,两个年龄组中性粒细胞的整合素表达在数量上均无显著差异。

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