Mojzisová A, Krizanová O, Záciková L, Komínková V, Ondrias K
Institute of Molecular Physiology and Genetics, Slovak Academy of Sciences, Bratislava, Slovak Republic.
Pflugers Arch. 2001 Feb;441(5):674-7. doi: 10.1007/s004240000465.
Nicotinic acid adenine dinucleotide phosphate (NAADP), a molecule derived from nicotinamide adenine dinucleotide phosphate (NADP+), is a recently identified nucleotide that activates Ca2+ release from intracellular stores in invertebrate eggs and in mammalian cells. NAADP could function as an intracellular messenger for mobilizing internal Ca2+ stores, however the targets and nature of NAADP-induced Ca2+ release are unknown. We report here that NAADP (3-10 microM) induces Ca2+ release from rat heart microsomes and that NAADP (1-10 microM) activates single ryanodine receptor/calcium release channels (RyR2) from dog heart incorporated into bilayer lipid membranes. The results indicate that NAADP may play a role in cardiac excitation-contraction coupling by acting on RyR2 channels.
烟酰胺腺嘌呤二核苷酸磷酸(NAADP)是一种由烟酰胺腺嘌呤二核苷酸磷酸(NADP+)衍生而来的分子,是最近发现的一种核苷酸,可激活无脊椎动物卵和哺乳动物细胞内储存库中的Ca2+释放。NAADP可能作为一种细胞内信使来动员细胞内的Ca2+储存库,然而,NAADP诱导Ca2+释放的靶点和性质尚不清楚。我们在此报告,NAADP(3-10 microM)可诱导大鼠心脏微粒体释放Ca2+,且NAADP(1-10 microM)可激活整合到双层脂质膜中的犬心脏单个兰尼碱受体/钙释放通道(RyR2)。结果表明,NAADP可能通过作用于RyR2通道在心脏兴奋-收缩偶联中发挥作用。