Naval Research Laboratory , Chemistry Division, Bio/Analytical Chemistry Section, Code 6112, 4555 Overlook Avenue SW, Washington, District of Columbia 20375, United States.
LumaCyte, LLC , 1145 River Road, Suite 16, Charlottesville, Virginia 22901, United States.
Anal Chem. 2017 Oct 3;89(19):10296-10302. doi: 10.1021/acs.analchem.7b01983. Epub 2017 Sep 21.
Understanding the interaction between macrophage cells and Bacillus anthracis spores is of significant importance with respect to both anthrax disease progression, spore detection for biodefense, as well as understanding cell clearance in general. While most detection systems rely on specific molecules, such as nucleic acids or proteins and fluorescent labels to identify the target(s) of interest, label-free methods probe changes in intrinsic properties, such as size, refractive index, and morphology, for correlation with a particular biological event. Optical chromatography is a label free technique that uses the balance between optical and fluidic drag forces within a microfluidic channel to determine the optical force on cells or particles. Here we show an increase in the optical force experienced by RAW264.7 macrophage cells upon the uptake of both microparticles and B. anthracis Sterne 34F2 spores. In the case of spores, the exposure was detected in as little as 1 h without the use of antibodies or fluorescent labels of any kind. An increase in the optical force was also seen in macrophage cells treated with cytochalasin D, both with and without a subsequent exposure to spores, indicating that a portion of the increase in the optical force arises independent of phagocytosis. These results demonstrate the capability of optical chromatography to detect subtle biological differences in a rapid and sensitive manner and suggest future potential in a range of applications, including the detection of biological threat agents for biodefense and pathogens for the prevention of sepsis and other diseases.
理解巨噬细胞与炭疽芽孢杆菌孢子之间的相互作用,对于炭疽病的进展、生物防御中的孢子检测以及一般的细胞清除机制都具有重要意义。虽然大多数检测系统依赖于特定的分子,如核酸或蛋白质和荧光标记物来识别感兴趣的目标,但无标记方法则探测固有特性的变化,如大小、折射率和形态,以与特定的生物事件相关联。光学色谱是一种无标记技术,它利用微流道内的光学和流体阻力之间的平衡来确定细胞或颗粒的光学力。在这里,我们展示了 RAW264.7 巨噬细胞在摄取微颗粒和炭疽芽孢杆菌 Sterne 34F2 孢子后,所经历的光学力的增加。在孢子的情况下,无需使用任何抗体或荧光标记,在 1 小时内即可检测到暴露。在用细胞松弛素 D 处理的巨噬细胞中也观察到光学力的增加,无论是在随后暴露于孢子之前还是之后,这表明光学力的增加有一部分是独立于吞噬作用的。这些结果表明光学色谱法具有快速、灵敏地检测细微生物差异的能力,并表明在包括生物防御中的生物威胁剂检测和预防败血症和其他疾病的病原体检测在内的一系列应用中具有未来的潜力。