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肿瘤坏死因子-α诱导的白细胞黏附和微血管通透性。

Tumor necrosis factor-alpha-induced leukocyte adhesion and microvessel permeability.

作者信息

Zeng Min, Zhang Hong, Lowell Clifford, He Pingnian

机构信息

Department of Physiology and Pharmacology, School of Medicine, West Virginia University, Morgantown 26506-9229, USA.

出版信息

Am J Physiol Heart Circ Physiol. 2002 Dec;283(6):H2420-30. doi: 10.1152/ajpheart.00787.2001. Epub 2002 Aug 8.

Abstract

The objective of this study was to investigate whether leukocyte adhesion and/or emigration are critical steps in increased microvessel permeability during acute inflammation. To conduct this study, we combined autologous blood perfusion with a single microvessel perfusion technique, which allows microvessel permeability to be measured precisely after the endothelium has interacted with blood-borne stimuli. Experiments were carried out in intact venular microvessels in rat mesenteries. Firm attachment of leukocytes to endothelial cells was induced by intravenous injection of TNF-alpha (3.5 microg/kg) and resuming autoperfusion in a precannulated microvessel. Leukocyte emigration was facilitated by superfusion of formyl-Met-Leu-Phe-OH. Microvessel permeability was measured as hydraulic conductivity (L(p)) or the solute permeability coefficient to tetramethylrhodamine isothiocyanate-labeled alpha-lactalbumin before and after leukocyte adhesion and emigration in individually perfused microvessels. We found that perfusion of a microvessel with TNF-alpha did not affect basal microvessel permeability, but intravenous injection of TNF-alpha caused significant leukocyte adhesion. However, the significant leukocyte adhesion and emigration did not cause corresponding increases in either L(p) or solute permeability. Thus our results suggest that leukocyte adhesion and emigration do not necessarily increase microvessel permeability and the mechanisms that regulate the adhesion process act independently from mechanisms that regulate permeability. In addition, silver staining of endothelial boundaries demonstrated that leukocytes preferentially adhere at the junctions of endothelial cells. The appearance of the silver lines indicates that the TNF-alpha-induced firm adhesion of leukocyte to microvessel walls did not involve apparent changes in the junctional structure of endothelial cells, which is consistent with the results of permeability measurements.

摘要

本研究的目的是调查白细胞黏附及/或游出是否为急性炎症期间微血管通透性增加的关键步骤。为开展本研究,我们将自体血液灌注与单一微血管灌注技术相结合,该技术可在内皮细胞与血源性刺激相互作用后精确测量微血管通透性。实验在大鼠肠系膜完整的微静脉血管中进行。通过静脉注射TNF-α(3.5微克/千克)并在预先插管的微血管中恢复自身灌注来诱导白细胞与内皮细胞的牢固黏附。通过灌注甲酰甲硫氨酰亮氨酰苯丙氨酸-OH促进白细胞游出。在单独灌注的微血管中,于白细胞黏附及游出前后,将微血管通透性测量为水力传导率(L(p))或对异硫氰酸四甲基罗丹明标记的α-乳白蛋白的溶质渗透系数。我们发现,用TNF-α灌注微血管并不影响基础微血管通透性,但静脉注射TNF-α会导致显著的白细胞黏附。然而,显著的白细胞黏附及游出并未导致L(p)或溶质通透性相应增加。因此,我们的结果表明,白细胞黏附及游出不一定会增加微血管通透性,且调节黏附过程的机制与调节通透性的机制独立发挥作用。此外,内皮边界的银染显示白细胞优先在内皮细胞连接处黏附。银线的出现表明TNF-α诱导的白细胞与微血管壁的牢固黏附并不涉及内皮细胞连接结构的明显变化,这与通透性测量结果一致。

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