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登革2型病毒抑制体外巨核细胞集落形成,并诱导脐带血CD34+细胞在血小板生成素诱导下的巨核细胞分化过程发生凋亡。

Dengue 2 virus inhibits in vitro megakaryocytic colony formation and induces apoptosis in thrombopoietin-inducible megakaryocytic differentiation from cord blood CD34+ cells.

作者信息

Basu Atanu, Jain Preksha, Gangodkar Shobha V, Shetty Shrimati, Ghosh Kanjaksha

机构信息

National Institute of Virology ICMR, Pune, India.

出版信息

FEMS Immunol Med Microbiol. 2008 Jun;53(1):46-51. doi: 10.1111/j.1574-695X.2008.00399.x. Epub 2008 Mar 25.

Abstract

Thrombocytopenia is frequently associated with dengue virus infection in humans. Although antiplatelet immunopathogenic processes have been implicated in the origin of dengue-associated thrombocytopenia, the effect of dengue viruses on megakaryocyte differentiation remains incompletely understood. In this study, we examined the effect of human dengue 2 virus isolates on the in vitro growth and differentiation of thrombopoietin-induced megakaryopoiesis of cord blood CD34+ cells. Dengue 2 viruses, but not Japanese encephalitis virus, showed a dose-dependent inhibition of CFU-Mk. Viral antigens could be detected by an immunohistochemical technique in 3-5% of the early megakaryocytic progenitors by the 5th postexposure day in liquid cultures with cell loss, increased annexin V binding and active caspase-3 expression. In summary, dengue 2 viruses can inhibit in vitro megakaryopoiesis, as well as infect and induce apoptotic cell death in a subpopulation of early megakaryocytic progenitors. These events might contribute towards the origin of thrombocytopenia in dengue disease.

摘要

血小板减少症在人类中常与登革热病毒感染相关。尽管抗血小板免疫致病过程被认为与登革热相关血小板减少症的发病机制有关,但登革热病毒对巨核细胞分化的影响仍未完全明确。在本研究中,我们检测了人登革热2型病毒分离株对血小板生成素诱导的脐血CD34+细胞巨核细胞生成的体外生长和分化的影响。登革热2型病毒,而非日本脑炎病毒,对巨核细胞集落形成单位(CFU-Mk)呈现剂量依赖性抑制作用。在液体培养中,暴露后第5天,通过免疫组化技术可在3%-5%的早期巨核细胞祖细胞中检测到病毒抗原,同时伴有细胞丢失、膜联蛋白V结合增加和活性半胱天冬酶-3表达。总之,登革热2型病毒可抑制体外巨核细胞生成,并感染早期巨核细胞祖细胞亚群并诱导其凋亡性细胞死亡。这些事件可能是登革热疾病中血小板减少症的发病原因。

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