首页> 外文期刊>Veterinary Research Communications >Bluetongue virus – 23 stimulates inducible nitric oxide synthase expression and nitric oxide production in mononuclear cells of blood and/or regional lymphoid organs
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Bluetongue virus – 23 stimulates inducible nitric oxide synthase expression and nitric oxide production in mononuclear cells of blood and/or regional lymphoid organs

机译:蓝舌病毒– 23刺激血液和/或局部淋巴器官的单核细胞中诱导型一氧化氮合酶的表达和一氧化氮的产生

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摘要

Mononuclear leukocytes of peripheral blood mononuclear cells (PBMCs) and regional lymphoid organs (RLOs) play a critical role in primary BTV replication and subsequent viral dissemination to distant systemic organs. The lesions in animals develop primarily as a result of vascular insult, presumably induced by the activity of viral and/or proinflammatory vasoactive mediators. Hence, the current study was designed in sheep to investigate the responses of potent vasoactivators, inducible nitric oxide synthase (iNOS) and/or nitric oxide (NO) in mononuclear leukocytes of PBMCs and RLOs. The results show that BTV infection of sheep led to enhanced transcription of iNOS in PBMCs and in particular RLOs. The BTV RNAs and/or antigens were readily demonstrable in these mononuclear leukocytes, suggesting the possible role of BTV in iNOS induction. Moreover, upon in vitro infection of PBMCs with BTV-23, iNOS was up-regulated in time-dependent fashion and correlated with increased NO production. The results from these in vivo and in vitro studies thus suggest iNOS and NO produced by mononuclear leukocytes may potentially contribute to vascular-related pathology of BT.
机译:外周血单核细胞(PBMC)和区域淋巴器官(RLO)的单核白细胞在原发性BTV复制以及随后的病毒传播至远距离的全身器官中起关键作用。动物的病变主要是由于血管损伤导致的,据推测是由病毒和/或促炎性血管活性介质的活性诱导的。因此,目前的研究是在绵羊中进行的,旨在研究PBMC和RLO的单核白细胞中有效的血管活化剂,诱导型一氧化氮合酶(iNOS)和/或一氧化氮(NO)的反应。结果表明,绵羊的BTV感染导致PBMC(尤其是RLO)中iNOS的转录增强。在这些单核白细胞中很容易证明BTV RNA和/或抗原,这表明BTV在iNOS诱导中的可能作用。此外,在体外用PBV-23感染PBMC时,iNOS以时间依赖性方式上调,并与NO产生增加相关。这些体内和体外研究的结果表明,单核白细胞产生的iNOS和NO可能与BT的血管相关病理有关。

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