Department of Chemical and Systems Biology, Stanford University, Stanford, CA 94305, USA.
Proc Natl Acad Sci U S A. 2013 May 21;110(21):8567-72. doi: 10.1073/pnas.1218336110. Epub 2013 May 6.
Interactions among neighboring cells underpin many physiological processes ranging from early development to immune responses. When these interactions do not function properly, numerous pathologies, including infection and cancer, can result. Molecular imaging technologies, especially optical imaging, are uniquely suited to illuminate complex cellular interactions within the context of living tissues in the body. However, no tools yet exist that allow the detection of microscopic events, such as two cells coming into close proximity, on a global, whole-animal scale. We report here a broadly applicable, longitudinal strategy for probing interactions among cells in living subjects. This approach relies on the generation of bioluminescent light when two distinct cell populations come into close proximity, with the intensity of the optical signal correlating with relative cellular location. We demonstrate the ability of this reporter strategy to gauge cell-cell proximity in culture models in vitro and then evaluate this approach for imaging tumor-immune cell interactions using a murine breast cancer model. In these studies, our imaging strategy enabled the facile visualization of features that are otherwise difficult to observe with conventional imaging techniques, including detection of micrometastatic lesions and potential sites of tumor immunosurveillance. This proximity reporter will facilitate probing of numerous types of cell-cell interactions and will stimulate the development of similar techniques to detect rare events and pathological processes in live animals.
细胞间的相互作用是许多生理过程的基础,从早期发育到免疫反应。当这些相互作用不能正常发挥作用时,就会导致许多疾病,包括感染和癌症。分子成像技术,特别是光学成像,非常适合在体内活体组织的背景下阐明复杂的细胞相互作用。然而,目前还没有工具可以检测到微观事件,例如两个细胞接近。我们在这里报告了一种广泛适用于探测活体动物中细胞间相互作用的纵向策略。这种方法依赖于当两个不同的细胞群体接近时产生生物发光,光学信号的强度与相对细胞位置相关。我们证明了这种报告基因策略在体外培养模型中测量细胞-细胞接近程度的能力,然后使用小鼠乳腺癌模型评估这种方法用于成像肿瘤-免疫细胞相互作用。在这些研究中,我们的成像策略使我们能够轻松地观察到常规成像技术难以观察到的特征,包括检测微转移病灶和肿瘤免疫监视的潜在部位。这种接近报告基因将促进对多种细胞-细胞相互作用的探测,并将刺激类似技术的发展,以检测活体动物中罕见事件和病理过程。