Neuronal Trafficking Laboratory, Queensland Brain Institute and School of Biomedical Sciences, The University of Queensland, Queensland 4072, Australia.
Prog Lipid Res. 2011 Jan;50(1):52-61. doi: 10.1016/j.plipres.2010.08.001. Epub 2010 Aug 10.
Phosphoinositides are a group of phospholipids whose inositol headgroups can be phosphorylated at three distinct positions thereby generating seven different isotypes. The conversion between these lipid species depends on the activity of specific sets of phosphoinositide kinases and phosphatases whose targeting and activity is critical to establish the landscape of phosphoinositides on the cytosol-facing hemi-membrane of all organelles and plasmalemma. Phosphoinositides play pleiotropic roles ranging from signalling and membrane trafficking to modulation of ion channels and survival. In neurons and neurosecretory cells, whose main function is to communicate through the release of neurotransmitter, most of the work has focused on the role played by phosphatidylinositol (4,5) bisphosphate in controlling the mechanism underpinning neurotransmitter release through the fusion of secretory vesicles with the plasmalemma. Emerging evidence supports a multi-faceted regulation of neuroexocytosis by 3-phosphorylated phosphoinositides. In this review, we summarise the molecular mechanism by which these lipids control exocytosis and how minute changes in their metabolism can have devastating effects in the nervous system and lead to neurodegeneration.
磷脂酰肌醇是一类磷脂,其肌醇头部可在三个不同位置磷酸化,从而产生七种不同的异构体。这些脂质种类之间的转化取决于特定的磷脂酰肌醇激酶和磷酸酶的活性,其靶向和活性对于在所有细胞器和质膜的质膜面向半膜上建立磷脂酰肌醇景观至关重要。磷脂酰肌醇发挥着多种作用,从信号传递和膜运输到调节离子通道和存活。在神经元和神经分泌细胞中,其主要功能是通过释放神经递质进行通信,大多数工作都集中在磷脂酰肌醇(4,5)双磷酸在通过与质膜融合控制神经递质释放的机制中的作用。新出现的证据支持 3 位磷酸化的磷脂酰肌醇对神经胞吐作用的多方面调节。在这篇综述中,我们总结了这些脂质控制胞吐作用的分子机制,以及它们代谢的微小变化如何对神经系统产生破坏性影响并导致神经退行性变。