2-Aminoethyl diphenylborinate analogues: selective inhibition for store-operated Ca2+ entry |
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Authors: | Zhou Hong Iwasaki Hirohide Nakamura Takeshi Nakamura Kyoko Maruyama Takayuki Hamano Shin-ichi Ozaki Shoichiro Mizutani Akihiro Mikoshiba Katsuhiko |
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Affiliation: | The Division of Molecular Neurobiology, Institute of Medical Sciences, University of Tokyo, 4-6-1 Shirokanedai, Tokyo 108-8639, Japan. |
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Abstract: | Capacitative calcium entry (CCE), the mechanism that replenishes the internal Ca2+ stores with Ca2+ from the extracellular milieu in response to depletion of the store, is mediated by Ca2+ channels in the plasma membrane generally referred to as store-operated channels (SOCs). However, the roles of SOCs in the more physiological context have been fully elucidated. 2-Aminoethyl diphenylborinate (2-APB) strongly inhibits SOCs, as well as inositol-1,4,5 trisphosphate (IP3) receptors. In the present study, we screened a library of 166 2-APB analogues for effects on CCE and IP3-induced Ca2+ release in order to discover specific SOC inhibitors, and found that some blocked both store-operated and receptor-operated Ca2+ influx more strongly and selectively than 2-APB. Indeed, these new compounds ceased the prolonged intracellular Ca2+ oscillations induced by a low concentration of ATP in CHO-K1 cells. These novel SOC inhibitors will be valuable pharmacological and biochemical tools for elucidating the physiological roles. |
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Keywords: | [Ca2+]i, intracellular Ca2+ concentration IP3R, inositol 1,4,5-trisphosphate receptor ER, endoplasmic reticulum CCE, capacitative calcium entry SOC, store-operated channel TRP, transient receptor potential 2-APB, 2-aminoethyl diphenylborinate CHO, Chinese hamster ovary HBSS, Hepes-buffered salt solution TG, thapsigargin SERCA, sarco/endoplasmic reticulum Ca2+-ATPase IICR, IP3-induced Ca2+ release |
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