CAS Key Laboratory for Biomedical Effects of Nanomaterials and Nanosafety and CAS Center for Excellence in Nanoscience, National Center for Nanoscience and Technology, Beijing, China.
College of Materials Science and Optoelectronic Technology, University of Chinese Academy of Sciences, Beijing, China.
Nat Biomed Eng. 2022 Sep;6(9):1074-1084. doi: 10.1038/s41551-022-00932-z. Epub 2022 Sep 1.
The in vivo optical imaging of RNA biomarkers of inflammation is hindered by low signal-to-background ratios, owing to non-specific signal amplification in healthy tissues. Here we report the design and in vivo applicability, for the imaging of inflammation-associated messenger RNAs (mRNAs), of a molecular beacon bearing apurinic/apyrimidinic sites, whose amplification of fluorescence is triggered by human apurinic/apyrimidinic endonuclease 1 on translocation from the nucleus into the cytoplasm specifically in inflammatory cells. We assessed the sensitivity and tissue specificity of an engineered molecular beacon targeting interleukin-6 (IL-6) mRNA in live mice, by detecting acute inflammation in their paws and drug-induced inflammation in their livers. This enzymatic-amplification strategy may enable the specific and sensitive imaging of other disease-relevant RNAs in vivo.
体内炎症 RNA 生物标志物的光学成像受到低信号背景比的限制,这是由于健康组织中的非特异性信号放大。在这里,我们报告了一种分子信标的设计和体内适用性,该分子信标带有无嘌呤/无嘧啶位点,其荧光的放大是由人无嘌呤/无嘧啶内切核酸酶 1 在核内易位到细胞质中特异性触发的,仅在炎症细胞中。我们通过检测活鼠爪子中的急性炎症和肝脏中的药物诱导性炎症,评估了针对白细胞介素 6 (IL-6) mRNA 的工程分子信标的灵敏度和组织特异性。这种酶促扩增策略可能使其他与疾病相关的 RNA 在体内的特异性和敏感成像成为可能。