Galione A, Parrington J, Dowden J
Department of Pharmacology, University of Oxford, Mansfield Road, Oxford OX1 3QT.
Br J Pharmacol. 2004 Aug;142(8):1203-7. doi: 10.1038/sj.bjp.0705888. Epub 2004 Jul 20.
NAADP is a recently described calcium-mobilizing messenger. First discovered as a potent calcium-releasing molecule in sea urchin eggs, its actions have now been reported in several mammalian cell types. In the sea urchin egg, NAADP-sensitive calcium release channels appear distinct from inositol trisphosphate or ryanodine receptors, and are mainly localized to acidic compartments. In this study, Billington et al. extend the pharmacology of the putative NAADP receptor utilizing molecules unrelated to NAADP itself. This work may provide an important step in developing selective NAADP receptor modulators that will help define the role of NAADP in cell signalling.
NAADP是一种最近被描述的钙动员信使分子。它最初作为一种在海胆卵中具有强大钙释放能力的分子被发现,现在其作用已在多种哺乳动物细胞类型中被报道。在海胆卵中,对NAADP敏感的钙释放通道似乎与肌醇三磷酸或兰尼碱受体不同,并且主要定位于酸性区室。在这项研究中,比林顿等人利用与NAADP本身无关的分子扩展了假定的NAADP受体的药理学研究。这项工作可能为开发选择性NAADP受体调节剂迈出重要一步,这将有助于明确NAADP在细胞信号传导中的作用。