Store-Operated Calcium Entry in Mouse Cardiomyocytes


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Аннотация

The fluorescent dye fura-2 AM was employed to record activation of Ca2+ entry in response to a decrease in Ca2+ concentration in the endoplasmic reticulum. Using whole-cell voltage clamp technique, we revealed Ca2+ currents with an amplitude of 0.46±0.13 pA/pF that passed through selective channels with current-voltage characteristics similar to those of classical store-operated CRAC channels. These currents were sensitive to 2-APB (50 μM), an inhibitor of store-operated channels. The data suggest that store-operated calcium entry is a characteristic feature of mature ventricular cardiomyocytes. Pathological alterations in store-operated Ca2+ entry can be implicated in the development of heart diseases.

Авторлар туралы

K. Gusev

Department of Ion Channels of Cell Membranes, Institute of Cytology, Russian Academy of Science

Хат алмасуға жауапты Автор.
Email: k.o.gusev@gmail.com
Ресей, St. Petersburg

V. Vigont

Department of Ion Channels of Cell Membranes, Institute of Cytology, Russian Academy of Science

Email: k.o.gusev@gmail.com
Ресей, St. Petersburg

D. Grekhnev

Department of Ion Channels of Cell Membranes, Institute of Cytology, Russian Academy of Science

Email: k.o.gusev@gmail.com
Ресей, St. Petersburg

A. Shalygin

Department of Ion Channels of Cell Membranes, Institute of Cytology, Russian Academy of Science

Email: k.o.gusev@gmail.com
Ресей, St. Petersburg

L. Glushankova

Department of Ion Channels of Cell Membranes, Institute of Cytology, Russian Academy of Science

Email: k.o.gusev@gmail.com
Ресей, St. Petersburg

E. Kaznacheeva

Department of Ion Channels of Cell Membranes, Institute of Cytology, Russian Academy of Science

Email: k.o.gusev@gmail.com
Ресей, St. Petersburg


© Springer Science+Business Media, LLC, part of Springer Nature, 2019

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