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纤连蛋白黏附的单核细胞表达组织因子和组织因子途径抑制物,而内毒素刺激的单核细胞主要表达组织因子:生理和病理意义

Fibronectin-adherent monocytes express tissue factor and tissue factor pathway inhibitor whereas endotoxin-stimulated monocytes primarily express tissue factor: physiologic and pathologic implications.

作者信息

Bajaj M S, Ghosh M, Bajaj S P

机构信息

Department of Medicine, David Geffen School of Medicine, and UCLA/Orthopedic Hospital, Los Angeles, CA 90095-1690, USA.

出版信息

J Thromb Haemost. 2007 Jul;5(7):1493-9. doi: 10.1111/j.1538-7836.2007.02604.x. Epub 2007 Apr 27.

Abstract

BACKGROUND

Monocytes are critical cells in initiating physiologic and/or pathologic tissue factor (TF)-induced intravascular and extravascular coagulation. Monocytes constitutively express small amounts of TF and tissue factor pathway inhibitor (TFPI). Non-adherent lipopolysaccharide (LPS)-stimulated monocytes express significant amounts of TF; however, increased expression of TFPI by these cells is controversial. Further, whether fibronectin-adherent monocytes (mimicking conditions in the extravascular space) express sufficient TFPI to inhibit TF-procoagulant activity (PCA) is unknown.

OBJECTIVE

To compare TF and TFPI expression by fibronectin-adherent and LPS-stimulated non-adherent monocytes.

METHODS

Monocytes were isolated from normal peripheral blood, adhered to fibronectin or stimulated with lipopolysaccharide (LPS) under non-adherent conditions and examined for expression of TF and TFPI using quantitative real-time reverse transcription-polymerase chain reaction (RT-PCR), ELISA and factor X (FX) activation.

RESULTS

Under LPS-free conditions, the fibronectin-adherent monocyte TF mRNA, antigen and activity were markedly upregulated. Notably, cell and microparticle (MP)-associated TF and alternatively spliced TF (asTF) were all upregulated. TFPI mRNA and antigen were also upregulated in the fibronectin-adherent monocytes, which significantly inhibited TF-PCA. TFPI mRNAs for both alpha and beta forms were detected. The peak in TFPI activity occurred in tandem with the peak in TF-PCA. In contrast, LPS-stimulated monocytes, which expressed cell and MP-associated TF and asTF, demonstrated only minimal expression of TFPI as determined by mRNA, antigen or inhibition of TF activity.

CONCLUSION

Both LPS-stimulated and fibronectin-adherent monocytes demonstrate a procoagulant phenotype by expressing TF but only fibronectin-adherent monocytes express significant amounts of TFPI to control thrombin generation and fibrin formation in the context of extravascular space.

摘要

背景

单核细胞是启动生理性和/或病理性组织因子(TF)诱导的血管内和血管外凝血的关键细胞。单核细胞组成性表达少量的TF和组织因子途径抑制剂(TFPI)。非黏附的脂多糖(LPS)刺激的单核细胞表达大量的TF;然而,这些细胞中TFPI表达的增加存在争议。此外,纤连蛋白黏附的单核细胞(模拟血管外空间的情况)是否表达足够的TFPI来抑制TF促凝活性(PCA)尚不清楚。

目的

比较纤连蛋白黏附的单核细胞和LPS刺激的非黏附单核细胞中TF和TFPI的表达。

方法

从正常外周血中分离单核细胞,使其黏附于纤连蛋白或在非黏附条件下用脂多糖(LPS)刺激,然后使用定量实时逆转录-聚合酶链反应(RT-PCR)、酶联免疫吸附测定(ELISA)和因子X(FX)激活来检测TF和TFPI的表达。

结果

在无LPS条件下,纤连蛋白黏附的单核细胞TF mRNA、抗原和活性显著上调。值得注意的是,细胞和微粒(MP)相关的TF以及可变剪接的TF(asTF)均上调。TFPI mRNA和抗原在纤连蛋白黏附的单核细胞中也上调,这显著抑制了TF-PCA。检测到α和β两种形式的TFPI mRNA。TFPI活性的峰值与TF-PCA的峰值同时出现。相比之下,LPS刺激的单核细胞表达细胞和MP相关的TF以及asTF,但通过mRNA、抗原或TF活性抑制测定,其TFPI表达仅为最低水平。

结论

LPS刺激的单核细胞和纤连蛋白黏附的单核细胞通过表达TF均表现出促凝表型,但只有纤连蛋白黏附的单核细胞表达大量的TFPI以在血管外空间的情况下控制凝血酶生成和纤维蛋白形成。

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