Sawada Keisuke, Echigo Noriko, Juge Narinobu, Miyaji Takaaki, Otsuka Masato, Omote Hiroshi, Yamamoto Akitsugu, Moriyama Yoshinori
Department of Membrane Biochemistry, Okayama University Graduate School of Medicine, Dentistry, and Pharmaceutical Sciences, Okayama University, Okayama 700-8530, Japan.
Proc Natl Acad Sci U S A. 2008 Apr 15;105(15):5683-6. doi: 10.1073/pnas.0800141105. Epub 2008 Mar 28.
ATP is a major chemical transmitter in purinergic signal transmission. Before secretion, ATP is stored in secretory vesicles found in purinergic cells. Although the presence of active transport mechanisms for ATP has been postulated for a long time, the proteins responsible for its vesicular accumulation remains unknown. The transporter encoded by the human and mouse SLC17A9 gene, a novel member of an anion transporter family, was predominantly expressed in the brain and adrenal gland. The mouse and bovine counterparts were associated with adrenal chromaffin granules. Proteoliposomes containing purified transporter actively took up ATP, ADP, and GTP by using membrane potential as the driving force. The uptake properties of the reconstituted transporter were similar to that of the ATP uptake by synaptic vesicles and chromaffin granules. Suppression of endogenous SLC17A9 expression in PC12 cells decreased exocytosis of ATP. These findings strongly suggest that SLC17A9 protein is a vesicular nucleotide transporter and should lead to the elucidation of the molecular mechanism of ATP secretion in purinergic signal transmission.
三磷酸腺苷(ATP)是嘌呤能信号传递中的一种主要化学递质。在分泌之前,ATP储存在嘌呤能细胞中的分泌囊泡内。尽管长期以来一直假定存在ATP的主动转运机制,但负责其在囊泡内积聚的蛋白质仍不清楚。人及小鼠SLC17A9基因编码的转运体是阴离子转运体家族的一个新成员,主要在脑和肾上腺中表达。小鼠和牛的相应转运体与肾上腺嗜铬颗粒相关。含有纯化转运体的蛋白脂质体以膜电位为驱动力,主动摄取ATP、二磷酸腺苷(ADP)和三磷酸鸟苷(GTP)。重组转运体的摄取特性与突触囊泡和嗜铬颗粒摄取ATP的特性相似。PC12细胞中内源性SLC17A9表达的抑制降低了ATP的胞吐作用。这些发现有力地表明,SLC17A9蛋白是一种囊泡核苷酸转运体,应该有助于阐明嘌呤能信号传递中ATP分泌的分子机制。