Department of Molecular, Cellular, and Developmental Biology, University of Michigan, Ann Arbor, MI, USA.
Bioessays. 2011 Jun;33(6):448-57. doi: 10.1002/bies.201000152. Epub 2011 Apr 28.
The direction and specificity of endolysosomal membrane trafficking is tightly regulated by various cytosolic and membrane-bound factors, including soluble NSF attachment protein receptors (SNAREs), Rab GTPases, and phosphoinositides. Another trafficking regulatory factor is juxta-organellar Ca(2+) , which is hypothesized to be released from the lumen of endolysosomes and to be present at higher concentrations near fusion/fission sites. The recent identification and characterization of several Ca(2+) channel proteins from endolysosomal membranes has provided a unique opportunity to examine the roles of Ca(2+) and Ca(2+) channels in the membrane trafficking of endolysosomes. SNAREs, Rab GTPases, and phosphoinositides have been reported to regulate plasma membrane ion channels, thereby suggesting that these trafficking regulators may also modulate endolysosomal dynamics by controlling Ca(2+) flux across endolysosomal membranes. In this paper, we discuss the roles of phosphoinositides, Ca(2+) , and potential interactions between endolysosomal Ca(2+) channels and phosphoinositides in endolysosomal dynamics.
内溶酶体膜运输的方向和特异性受到各种细胞质和膜结合因子的严格调节,包括可溶性 NSF 附着蛋白受体 (SNAREs)、Rab GTPases 和磷酸肌醇。另一个运输调节因子是邻近细胞器的 Ca(2+),它被假设从内溶酶体的腔中释放出来,并在融合/裂变部位附近以更高的浓度存在。最近从内溶酶体膜中鉴定和表征了几种 Ca(2+)通道蛋白,为研究 Ca(2+)和 Ca(2+)通道在内溶酶体膜运输中的作用提供了独特的机会。已经报道 SNAREs、Rab GTPases 和磷酸肌醇调节质膜离子通道,这表明这些运输调节剂也可以通过控制内溶酶体膜的 Ca(2+)通量来调节内溶酶体的动态。在本文中,我们讨论了磷酸肌醇、Ca(2+)以及内溶酶体 Ca(2+)通道和磷酸肌醇之间潜在相互作用在内溶酶体动力学中的作用。