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DNAzyme-Based Lithium-Selective Imaging Reveals Higher Lithium Accumulation in Bipolar Disorder Patient-Derived Neurons

[Image: see text] Lithium has been a drug for bipolar disorders (BD) for over 70 years; however, its usage has been limited by its narrow therapeutic window (between 0.6 and 1.2 mM). Understanding the cellular distribution of lithium ions (Li(+)) in patient cells will offer deep insight into this li...

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Detalles Bibliográficos
Autores principales: McGhee, Claire E., Yang, Zhenglin, Guo, Weijie, Wu, Yuting, Lyu, Mingkuan, DeLong, Cynthia J., Hong, Shanni, Ma, Yuan, McInnis, Melvin G., O’Shea, K. Sue, Lu, Yi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2021
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8614110/
https://www.ncbi.nlm.nih.gov/pubmed/34841055
http://dx.doi.org/10.1021/acscentsci.1c00843
Descripción
Sumario:[Image: see text] Lithium has been a drug for bipolar disorders (BD) for over 70 years; however, its usage has been limited by its narrow therapeutic window (between 0.6 and 1.2 mM). Understanding the cellular distribution of lithium ions (Li(+)) in patient cells will offer deep insight into this limitation, but selective imaging of Li(+) in living cells under biomedically relevant concentration ranges has not been achieved. Herein, we report in vitro selection and development of a Li(+)-specific DNAzyme fluorescent sensor with >100-fold selectivity over other biorelevant metal ions. This sensor allows comparative Li(+) visualization in HeLa cells, human neuronal progenitor cells (NPCs), and neurons derived from BD patients and healthy controls. Strikingly, we detected enhanced accumulation of Li(+) in cells derived from BD patients compared with healthy controls in differentiated neurons but not NPCs. These results establish the DNAzyme-based sensor as a novel platform for biomedical research into BD and related areas using lithium drugs.