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NKp44受体介导西尼罗河病毒和登革病毒的包膜糖蛋白与自然杀伤细胞的相互作用。

NKp44 receptor mediates interaction of the envelope glycoproteins from the West Nile and dengue viruses with NK cells.

作者信息

Hershkovitz Oren, Rosental Benyamin, Rosenberg Lior Ann, Navarro-Sanchez Martha Erika, Jivov Sergey, Zilka Alon, Gershoni-Yahalom Orly, Brient-Litzler Elodie, Bedouelle Hugues, Ho Joanna W, Campbell Kerry S, Rager-Zisman Bracha, Despres Philippe, Porgador Angel

机构信息

Shraga Segal Department of Microbiology and Immunology and National Institute for Biotechnology in the Negev, Ben Gurion University of the Negev, Beer Sheva, Israel.

出版信息

J Immunol. 2009 Aug 15;183(4):2610-21. doi: 10.4049/jimmunol.0802806. Epub 2009 Jul 27.

Abstract

Dengue virus (DV) and West Nile virus (WNV) have become a global concern due to their widespread distribution and their ability to cause a variety of human diseases. Antiviral immune defenses involve NK cells. In the present study, we investigated the interaction between NK cells and these two flaviviruses. We show that the NK-activating receptor NKp44 is involved in virally mediated NK activation through direct interaction with the flavivirus envelope protein. Recombinant NKp44 directly binds to purified DV and WNV envelope proteins and specifically to domain III of WNV envelope protein; it also binds to WNV virus-like particles. These WNV-virus-like particles and WNV-domain III of WNV envelope protein directly bind NK cells expressing high levels of NKp44. Functionally, interaction of NK cells with infective and inactivated WNV results in NKp44-mediated NK degranulation. Finally, WNV infection of cells results in increased binding of rNKp44 that is specifically inhibited by anti-WNV serum. WNV-infected target cells induce IFN-gamma secretion and augmented lysis by NKp44-expressing primary NK cells that are blocked by anti-NKp44 Abs. Our findings show that triggering of NK cells by flavivirus is mediated by interaction of NKp44 with the flavivirus envelope protein.

摘要

登革病毒(DV)和西尼罗河病毒(WNV)因其广泛传播以及引发多种人类疾病的能力而成为全球关注的焦点。抗病毒免疫防御涉及自然杀伤细胞(NK细胞)。在本研究中,我们调查了NK细胞与这两种黄病毒之间的相互作用。我们发现,NK细胞激活受体NKp44通过与黄病毒包膜蛋白直接相互作用,参与病毒介导的NK细胞激活。重组NKp44直接结合纯化的DV和WNV包膜蛋白,并特异性结合WNV包膜蛋白的结构域III;它还与WNV病毒样颗粒结合。这些WNV病毒样颗粒和WNV包膜蛋白的WNV结构域III直接结合表达高水平NKp44的NK细胞。在功能上,NK细胞与感染性和灭活的WNV相互作用导致NKp44介导的NK细胞脱颗粒。最后,细胞感染WNV导致rNKp44的结合增加,抗WNV血清可特异性抑制这种增加。WNV感染的靶细胞诱导γ干扰素分泌,并增强表达NKp44的原代NK细胞的裂解作用,抗NKp44抗体可阻断这种作用。我们的研究结果表明,黄病毒触发NK细胞是由NKp44与黄病毒包膜蛋白的相互作用介导的。

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