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首页> 外文期刊>Journal of Pathology: Journal of the Pathological Society of Great Britain and Ireland >Thrombospondin-1 inhibits Kaposi's sarcoma (KS) cell and HIV-1 Tat-induced angiogenesis and is poorly expressed in KS lesions.
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Thrombospondin-1 inhibits Kaposi's sarcoma (KS) cell and HIV-1 Tat-induced angiogenesis and is poorly expressed in KS lesions.

机译:血小板反应蛋白-1抑制卡波济肉瘤(KS)细胞和HIV-1 Tat诱导的血管生成,在KS病变中表达较差。

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摘要

Kaposi's sarcoma (KS), a neoplasm often associated with iatrogenic and acquired immunosuppression, is characterized by prominent angiogenesis. Angiogenic factors released by both KS and host cells, as well as HHV-8 and HIV viral products, have been implicated in the pathogenesis of this lesion. Angiogenesis is the result of imbalance among angiogenesis promoters and inhibitors, which disrupts homeostasis. The aim of this study was to investigate the expression and mechanism of KS control of thrombospondin-1 (TSP), a physiological inhibitor of angiogenesis. Immunohistochemical analysis of four KS lesions showed only spotty reactivity for TSP in the stroma and in less than 10 per cent of lesional blood vessels. In addition, the typical KS spindle cells were not stained. In agreement with these findings, decreased levels of TSP were measured with an ELISA assay in the supernatants of cultured KS cells, compared with endothelial cells. In vitro, TSP inhibited the endothelial cell proliferation and motility induced by KS cell supernatants. TSP also prevented endothelial cell motility induced by Tat, a product of HIV-1 endowed with angiogenic potential and implicated in the pathogenesis of AIDS-KS. In vivo, TSP inhibited the angiogenic activity exerted by Tat in the Matrigel sponge model. These results suggest that TSP down-regulation might be permissive for the development of KS-associated angiogenesis. Copyright 1999 John Wiley & Sons, Ltd.
机译:卡波西氏肉瘤(KS)是一种经常与医源性和获得性免疫抑制相关的肿瘤,其特征是血管生成显着。 KS和宿主细胞以及HHV-8和HIV病毒产物释放的血管生成因子均与该病变的发病机制有关。血管生成是血管生成促进剂和抑制剂之间失衡的结果,破坏了体内稳态。这项研究的目的是研究KS调节血小板生成素-1(TSP),一种血管生成的生理抑制剂的表达和机制。对四个KS病变的免疫组织化学分析显示,基质中以及不到10%的病变血管中TSP仅具有斑点反应性。另外,典型的KS纺锤体细胞未染色。与这些发现相一致,与内皮细胞相比,在培养的KS细胞的上清液中通过ELISA测定法测量了TSP水平降低。在体外,TSP抑制了KS细胞上清液诱导的内皮细胞增殖和运动。 TSP还阻止了由Tat诱导的内皮细胞运动,Tat是一种具有血管生成潜力并与AIDS-KS发病有关的HIV-1产物。在体内,TSP抑制了Tat在Matrigel海绵模型中发挥的血管生成活性。这些结果表明,TSP下调可能是与KS相关的血管生成发展的原因。版权所有1999 John Wiley&Sons,Ltd.

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