Tedeschi Giulia, Navarro Mariana X, Scipioni Lorenzo, Sondhi Tanvi K, Prescher Jennifer A, Digman Michelle A
Laboratory for Fluorescence Dynamics, Biomedical Engineering Department, University of California, Irvine, Irvine, California 92617, United States.
Department of Chemistry, University of California Irvine, Irvine, California 92617, United States.
Chem Biomed Imaging. 2024 Oct 3;2(11):765-774. doi: 10.1021/cbmi.4c00049. eCollection 2024 Nov 25.
Macrophages exhibit a spectrum of behaviors upon activation and are generally classified as one of two types: inflammatory (M1) or anti-inflammatory (M2). Tracking these phenotypes in living cells can provide insight into immune function but remains a challenging pursuit. Existing methods are mostly limited to static readouts or are difficult to employ for multiplexed imaging in complex 3D environments while maintaining cellular resolution. We aimed to fill this void using bioluminescent technologies. Here we report genetically engineered luciferase reporters for the long-term monitoring of macrophage polarization via spectral phasor analysis. M1- and M2-specific promoters were used to drive the expression of bioluminescent enzymes in macrophage cell lines. The readouts were multiplexed and discernible in both 2D and 3D formats with single-cell resolution in living samples. Collectively, this work expands the toolbox of methods for monitoring macrophage polarization and provides a blueprint for monitoring other multifaceted networks in heterogeneous environments.
巨噬细胞在激活后表现出一系列行为,通常分为两种类型之一:炎症性(M1)或抗炎性(M2)。在活细胞中追踪这些表型可以深入了解免疫功能,但仍然是一项具有挑战性的工作。现有方法大多限于静态读数,或者在复杂的3D环境中进行多重成像时难以应用,同时还要保持细胞分辨率。我们旨在利用生物发光技术填补这一空白。在此,我们报告了通过光谱相量分析对巨噬细胞极化进行长期监测的基因工程荧光素酶报告基因。M1和M2特异性启动子用于驱动巨噬细胞系中生物发光酶的表达。读数以2D和3D格式进行多重化,并且在活样本中具有单细胞分辨率时可辨别。总的来说,这项工作扩展了监测巨噬细胞极化的方法工具箱,并为监测异质环境中的其他多方面网络提供了蓝图。