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补体蛋白的非特异性吸附会影响金纳米材料的补体激活途径。

Non-specific adsorption of complement proteins affects complement activation pathways of gold nanomaterials.

作者信息

Quach Quang Huy, Kah James Chen Yong

机构信息

a Department of Biomedical Engineering , National University of Singapore , Singapore , Singapore.

b NUS Graduate School for Integrative Sciences and Engineering, National University of Singapore , Singapore , Singapore.

出版信息

Nanotoxicology. 2017 Apr;11(3):382-394. doi: 10.1080/17435390.2017.1306131. Epub 2017 Apr 3.

Abstract

The complement system is a key humoral component of innate immunity, serving as the first line of defense against intruders, including foreign synthetic nanomaterials. Although gold nanomaterials (AuNMs) are widely used in nanomedicine, their immunological response is not well understood. Using AuNMs of three shapes commonly used in biomedical applications: spherical gold nanoparticles, gold nanostars and gold nanorods, we demonstrated that AuNMs activated whole complement system, leading to the formation of SC5b-9 complex. All three complement pathways were simultaneously activated by all the AuNMs. Recognition molecules of the complement system interacted with all AuNMs in vitro, except for l-ficolin, but the correlation between these interactions and corresponding complement pathway activation was only observed in the classical and alternative pathways. We also observed the mediating role of complement activation in cellular uptake of all AuNMs by human U937 promonocytic cells, which expresses complement receptors. Taken together, our results highlighted the potential immunological challenges for clinical applications of AuNMs that were often overlooked.

摘要

补体系统是固有免疫的关键体液成分,作为抵御入侵者(包括外来合成纳米材料)的第一道防线。尽管金纳米材料(AuNMs)在纳米医学中广泛应用,但其免疫反应尚未得到充分了解。我们使用生物医学应用中常用的三种形状的AuNMs:球形金纳米颗粒、金纳米星和金纳米棒,证明AuNMs激活了整个补体系统,导致SC5b-9复合物的形成。所有三种补体途径均被所有AuNMs同时激活。补体系统的识别分子在体外与所有AuNMs相互作用,除了L-纤维胶凝蛋白,但这些相互作用与相应补体途径激活之间的相关性仅在经典途径和替代途径中观察到。我们还观察到补体激活在表达补体受体的人U937前单核细胞对所有AuNMs的细胞摄取中的介导作用。综上所述,我们的结果突出了AuNMs临床应用中常被忽视的潜在免疫挑战。

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