Store-Operated Calcium Entry in Mouse Cardiomyocytes


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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.

作者简介

K. Gusev

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

编辑信件的主要联系方式.
Email: k.o.gusev@gmail.com
俄罗斯联邦, St. Petersburg

V. Vigont

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

Email: k.o.gusev@gmail.com
俄罗斯联邦, St. Petersburg

D. Grekhnev

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

Email: k.o.gusev@gmail.com
俄罗斯联邦, St. Petersburg

A. Shalygin

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

Email: k.o.gusev@gmail.com
俄罗斯联邦, St. Petersburg

L. Glushankova

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

Email: k.o.gusev@gmail.com
俄罗斯联邦, St. Petersburg

E. Kaznacheeva

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

Email: k.o.gusev@gmail.com
俄罗斯联邦, St. Petersburg


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