Dawson A P, Comerford J G
School of Biological Sciences, University of East Anglia, Norwich, UK.
Cell Calcium. 1989 Jul;10(5):343-50. doi: 10.1016/0143-4160(89)90060-2.
Our initial observation that GTP could, under some experimental conditions, have profound effects on Ca2+ movements across endoplasmic reticulum membranes arose from attempts to increase the sensitivity of rat liver microsomes to inositol 1,4,5 trisphosphate (IP3). Most preparations of microsomal fractions from rat liver release only a very small percentage of accumulated Ca2+ on addition of IP3. We found, rather empirically, that the addition of microM concentrations of GTP greatly enhanced the amount of Ca2+ releasable by IP3. The initial, very appealing, hypothesis was to postulate a direct effect of GTP on the IP3-sensitive Ca2+ channel. This idea is no longer tenable, as will be described below. The more likely explanation, that GTP has its effect by either fusing small microsomal vesicles together or by allowing some form of communication between adjacent membranes is considerably more complex mechanistically and also possibly has far reaching implications for the mechanisms by which cells organise and maintain their reticular structures.
我们最初的观察结果是,在某些实验条件下,GTP可能会对钙离子跨内质网膜的移动产生深远影响,这一观察源于我们试图提高大鼠肝脏微粒体对肌醇1,4,5-三磷酸(IP3)的敏感性。大多数从大鼠肝脏制备的微粒体组分在添加IP3后,仅释放出极少量积累的钙离子。我们通过经验发现,添加微摩尔浓度的GTP可极大地增强IP3可释放的钙离子量。最初,一个非常吸引人的假设是假定GTP对IP3敏感的钙离子通道有直接作用。如下所述,这个想法已不再成立。更有可能的解释是,GTP通过将小的微粒体囊泡融合在一起,或者通过允许相邻膜之间某种形式的通讯来发挥作用,这在机制上要复杂得多,而且可能对细胞组织和维持其网状结构的机制也有深远影响。