Shaw Stanley Y, Westly Elizabeth C, Pittet Mikael J, Subramanian Aravind, Schreiber Stuart L, Weissleder Ralph
Broad Institute of Harvard and MIT, 7 Cambridge Center, Cambridge, MA 02142, USA.
Proc Natl Acad Sci U S A. 2008 May 27;105(21):7387-92. doi: 10.1073/pnas.0802878105. Epub 2008 May 20.
Our understanding of the biologic effects (including toxicity) of nanomaterials is incomplete. In vivo animal studies remain the gold standard; however, widespread testing remains impractical, and the development of in vitro assays that correlate with in vivo activity has proven challenging. Here, we demonstrate the feasibility of analyzing in vitro nanomaterial activity in a generalizable, systematic fashion. We assessed nanoparticle effects in a multidimensional manner, using multiple cell types and multiple assays that reflect different aspects of cellular physiology. Hierarchical clustering of these data identifies nanomaterials with similar patterns of biologic activity across a broad sampling of cellular contexts, as opposed to extrapolating from results of a single in vitro assay. We show that this approach yields robust and detailed structure-activity relationships. Furthermore, a subset of nanoparticles were tested in mice, and nanoparticles with similar activity profiles in vitro exert similar effects on monocyte number in vivo. These data suggest a strategy of multidimensional characterization of nanomaterials in vitro that can inform the design of novel nanomaterials and guide studies of in vivo activity.
我们对纳米材料的生物学效应(包括毒性)的理解并不完整。体内动物研究仍然是金标准;然而,广泛的测试仍然不切实际,并且与体内活性相关的体外分析方法的开发已被证明具有挑战性。在此,我们展示了以可推广、系统的方式分析体外纳米材料活性的可行性。我们使用多种细胞类型和反映细胞生理学不同方面的多种分析方法,以多维方式评估纳米颗粒的效应。这些数据的层次聚类识别出在广泛的细胞环境样本中具有相似生物活性模式的纳米材料,而不是从单一体外分析的结果进行推断。我们表明,这种方法产生了稳健且详细的构效关系。此外,对一部分纳米颗粒在小鼠中进行了测试,体外具有相似活性谱的纳米颗粒在体内对单核细胞数量产生相似的影响。这些数据表明了一种体外纳米材料多维表征策略,可为新型纳米材料的设计提供信息并指导体内活性研究。
Proc Natl Acad Sci U S A. 2008-5-27
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