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 Ca2+ 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 C...

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التفاصيل البيبلوغرافية
المؤلفون الرئيسيون: Mart Bittremieux, Katsuhiko Mikoshiba, Geert Bultynck
التنسيق: مقال
اللغة:English
منشور في: Elsevier 2017-06-01
سلاسل:Data in Brief
الموضوعات:
الوصول للمادة أونلاين:http://www.sciencedirect.com/science/article/pii/S2352340917301105
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author Mart Bittremieux
Katsuhiko Mikoshiba
Geert Bultynck
author_facet Mart Bittremieux
Katsuhiko Mikoshiba
Geert Bultynck
author_sort Mart Bittremieux
collection DOAJ
description DPB162-AE is a valuable tool to study store-operated Ca2+ 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 Ca2+ 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 Ca2+ entry, can deplete the endoplasmic reticulum Ca2+ store’ (M. Bittremieux, J. V. Gerasimenko, M. Schuermans, T. Luyten, E. Stapleton, K.J. Alzayady, et al., 2017) [1].
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spelling doaj.art-eba1af73fd3e4849b3cbdf376b51a3ba2022-12-21T18:47:58ZengElsevierData in Brief2352-34092017-06-0112C919610.1016/j.dib.2017.03.034Data on cytotoxicity in HeLa and SU-DHL-4 cells exposed to DPB162-AE compoundMart Bittremieux0Katsuhiko Mikoshiba1Geert Bultynck2KU Leuven, Laboratory of Molecular and Cellular Signaling, Department of Cellular and Molecular Medicine & Leuven Kanker Instituut, 3000 Leuven, BelgiumThe Laboratory for Developmental Neurobiology, Brain Science Institute, RIKEN, 2-1 Hirosawa, Wako, Saitama 351-0198, JapanKU Leuven, Laboratory of Molecular and Cellular Signaling, Department of Cellular and Molecular Medicine & Leuven Kanker Instituut, 3000 Leuven, BelgiumDPB162-AE is a valuable tool to study store-operated Ca2+ 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 Ca2+ 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 Ca2+ entry, can deplete the endoplasmic reticulum Ca2+ store’ (M. Bittremieux, J. V. Gerasimenko, M. Schuermans, T. Luyten, E. Stapleton, K.J. Alzayady, et al., 2017) [1].http://www.sciencedirect.com/science/article/pii/S2352340917301105DPB162-AECell toxicityCell linesCalcium
spellingShingle Mart Bittremieux
Katsuhiko Mikoshiba
Geert Bultynck
Data on cytotoxicity in HeLa and SU-DHL-4 cells exposed to DPB162-AE compound
Data in Brief
DPB162-AE
Cell toxicity
Cell lines
Calcium
title Data on cytotoxicity in HeLa and SU-DHL-4 cells exposed to DPB162-AE compound
title_full Data on cytotoxicity in HeLa and SU-DHL-4 cells exposed to DPB162-AE compound
title_fullStr Data on cytotoxicity in HeLa and SU-DHL-4 cells exposed to DPB162-AE compound
title_full_unstemmed Data on cytotoxicity in HeLa and SU-DHL-4 cells exposed to DPB162-AE compound
title_short Data on cytotoxicity in HeLa and SU-DHL-4 cells exposed to DPB162-AE compound
title_sort data on cytotoxicity in hela and su dhl 4 cells exposed to dpb162 ae compound
topic DPB162-AE
Cell toxicity
Cell lines
Calcium
url http://www.sciencedirect.com/science/article/pii/S2352340917301105
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AT geertbultynck dataoncytotoxicityinhelaandsudhl4cellsexposedtodpb162aecompound