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Sub-nanomolar sensitive GZnP3 reveals TRPML1-mediated neuronal Zn(2+) signals

Although numerous fluorescent Zn(2+) sensors have been reported, it is unclear whether and how Zn(2+) can be released from the intracellular compartments into the cytosol due to a lack of probes that can detect physiological dynamics of cytosolic Zn(2+). Here, we create a genetically encoded sensor,...

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Detalles Bibliográficos
Autores principales: Minckley, Taylor F., Zhang, Chen, Fudge, Dylan H., Dischler, Anna M., LeJeune, Kate D., Xu, Haoxing, Qin, Yan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6805855/
https://www.ncbi.nlm.nih.gov/pubmed/31641116
http://dx.doi.org/10.1038/s41467-019-12761-x
Descripción
Sumario:Although numerous fluorescent Zn(2+) sensors have been reported, it is unclear whether and how Zn(2+) can be released from the intracellular compartments into the cytosol due to a lack of probes that can detect physiological dynamics of cytosolic Zn(2+). Here, we create a genetically encoded sensor, GZnP3, which demonstrates unprecedented sensitivity for Zn(2+) at sub-nanomolar concentrations. Using GZnP3 as well as GZnP3-derived vesicular targeted probes, we provide the first direct evidence that Zn(2+) can be released from endolysosomal vesicles to the cytosol in primary hippocampal neurons through the TRPML1 channel. Such TRPML1-mediated Zn(2+) signals are distinct from Ca(2+) in that they are selectively present in neurons, sustain longer, and are significantly higher in neurites as compared to the soma. Together, our work not only creates highly sensitive probes for investigating sub-nanomolar Zn(2+) dynamics, but also reveals new pools of Zn(2+) signals that can play critical roles in neuronal function.