| Literature DB >> 32223138 |
Zheng-Min Yang1,2, Qing-Yuan Mo1, Ji-Man He1, Dong-Liang Mo1, Jun Li1, Hua Chen1, Shu-Lin Zhao1, Jiang-Ke Qin1.
Abstract
Monoamine oxidase A (MAO-A) is a promising diagnostic marker for cancer, depression, Parkinson's disease, and liver disease. The fluorescence detection of MAO-A in living animals is of extreme importance for the early diagnosis of related diseases. However, the development of specific and mitochondrial-targeted and near-infrared (NIR) fluorescence MAO-A probes is still inadequate. Here, we designed and synthesized four NIR fluorescence probes containing a dihydroxanthene (DH) skeleton to detect MAO-A in complex biological systems. The specificity of our representative probe DHMP2 displays a 31-fold fluorescence turn-on in vitro, and it can effectively accumulate in the mitochondria and specifically detect the endogenous MAO-A concentrations in PC-3 and SH-SY5Y cell lines. Furthermore, the probe DHMP2 can be used to visualize the endogenous MAO-A activity in zebrafish and tumor-bearing mice. More importantly, it is the first time that the MAO-A activity of hepatic fibrosis tissues is detected through the probe DHMP2. The present study shows that the synthesized DHMP2 might serve as a potential tool for monitoring MAO-A activity in vivo and diagnosing related diseases.Entities:
Keywords: bioimaging; hepatic fibrosis; mitochondrial-targeted; monoamine oxidase A; near-infrared fluorescence probe
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Year: 2020 PMID: 32223138 DOI: 10.1021/acssensors.9b02116
Source DB: PubMed Journal: ACS Sens ISSN: 2379-3694 Impact factor: 7.711