| Literature DB >> 25244053 |
Liang He1, Cai-Ping Tan, Rui-Rong Ye, Yi-Zhi Zhao, Ya-Hong Liu, Qiang Zhao, Liang-Nian Ji, Zong-Wan Mao.
Abstract
During autophagy, the intracellular components are captured in autophagosomes and delivered to lysosomes for degradation and recycling. Changes in lysosomal trafficking and contents are key events in the regulation of autophagy, which has been implicated in many physiological and pathological processes. In this work, two iridium(III) complexes (LysoIr1 and LysoIr2) are developed as theranostic agents to monitor autophagic lysosomes. These complexes display lysosome-activated phosphorescence and can specifically label lysosomes with high photostability. Simultaneously, they can induce autophagy potently without initiating an apoptosis response. We demonstrate that LysoIr2 can effectively implement two functions, namely autophagy induction and lysosomal tracking, in the visualization of autophagosomal-lysosomal fusion. More importantly, they display strong two-photon excited fluorescence (TPEF), which is favorable for live cell imaging and in vivo applications.Entities:
Keywords: autophagy; bioinorganic chemistry; iridium; probe; theranostic
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Year: 2014 PMID: 25244053 DOI: 10.1002/anie.201407468
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336