乙二胺四乙酸
EGTA公司
螯合作用
化学
受体
细胞外
生物化学
分子生物学
细胞生物学
钙
生物
有机化学
作者
Masahito Deai,Rin Oya,Naosi Saso,Asahi Tanaka,Izumi Uchida,Yuta Miyake,Ryo Tachihara,Miku Otsugu,Ayumi Mine,Kōichi Sato,Hideaki Tomura
标识
DOI:10.1016/j.bbrc.2022.07.110
摘要
Ethylenediaminetetraacetic acid (EDTA) is a chelating agent that binds tightly to metal ions. We found that cAMP response element (CRE)-driven promoter activity by protons was enhanced by EDTA in human T-cell death-associated gene 8 (TDAG8)-overexpressed HEK293T cells. The enhancing action by EDTA was also detected by proton-induced cAMP production that is located upstream from the CRE-driven promoter activity even at physiological proton concentration pH7.4. The proton-induced CRE-driven promoter activity was not enhanced by other chelating agents, ethylene glycol tetraacetic acid (EGTA) and sodium citrate. The enhanced CRE-driven promoter activity by EDTA was not attenuated by increasing the extracellular calcium ion concentration. These results indicate that the EDTA-enhancing action may not be due to its chelating action but might rather be another EDTA-specific effect. Enhanced cAMP production by EDTA was also detected in a human leukemia cell line HL-60, in which TDAG8 and OGR1 (ovarian cancer G-protein-coupled receptor 1) were endogenously expressed, suggesting that the medical use of EDTA would influence the physiological and pathophysiological functions of hematopoietic cells.
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