Data on cytotoxicity in HeLa and SU-DHL-4 cells exposed to DPB162-AE compound

DPB162-AE is a valuable tool to study store-operated Ca(2+) entry (SOCE), as this compound was developed as a 2-APB analog that inhibits SOCE more potently and more selectively than 2-APB itself. In addition to this, we showed that, in some conditions, DPB162-AE can deplete the endoplasmic reticulum...

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Detalles Bibliográficos
Autores principales: Bittremieux, Mart, Mikoshiba, Katsuhiko, Bultynck, Geert
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2017
Materias:
Data Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5377240/
https://www.ncbi.nlm.nih.gov/pubmed/28393091
http://dx.doi.org/10.1016/j.dib.2017.03.034
Descripción
Sumario:DPB162-AE is a valuable tool to study store-operated Ca(2+) entry (SOCE), as this compound was developed as a 2-APB analog that inhibits SOCE more potently and more selectively than 2-APB itself. In addition to this, we showed that, in some conditions, DPB162-AE can deplete the endoplasmic reticulum Ca(2+) stores in intact cells, including the cervical carcinoma HeLa cell line and the diffuse large B-cell lymphoma SU-DHL-4 cell line. Here, we present data regarding the toxicity of DPB162-AE in HeLa and SU-DHL-4 cells. For further interpretation of the data presented in this article, please see the research article ‘DPB162-AE, an inhibitor of store-operated Ca(2+) entry, can deplete the endoplasmic reticulum Ca(2+) store’ (M. Bittremieux, J. V. Gerasimenko, M. Schuermans, T. Luyten, E. Stapleton, K.J. Alzayady, et al., 2017) [1].

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