Ikeda Mika, Kihara Akio, Denpoh Aki, Igarashi Yasuyuki
Laboratory of Biomembrane and Biofunctional Chemistry, Faculty of Pharmaceutical Sciences, Hokkaido University, Sapporo 060-0812, Japan.
Mol Biol Cell. 2008 May;19(5):1922-31. doi: 10.1091/mbc.e07-08-0806. Epub 2008 Feb 20.
Biological membranes consist of lipid bilayers. The lipid compositions between the two leaflets of the plasma membrane differ, generating lipid asymmetry. Maintenance of proper lipid asymmetry is physiologically quite important, and its collapse induces several cellular responses including apoptosis and platelet coagulation. Thus, a change in lipid asymmetry must be restored to maintain "lipid asymmetry homeostasis." However, to date no lipid asymmetry-sensing proteins or any related downstream signaling pathways have been identified. We recently demonstrated that expression of the putative yeast sphingoid long-chain base transporter/translocase Rsb1 is induced when glycerophospholipid asymmetry is altered. Using mutant screening, we determined that the pH-responsive Rim101 pathway, the protein kinase Mck1, and the transcription factor Mot3 all act in lipid asymmetry signaling, and that the Rim101 pathway was activated in response to a change in lipid asymmetry. The activated transcription factor Rim101 induces Rsb1 expression via repression of another transcription repressor, Nrg1. Changes in lipid asymmetry are accompanied by cell surface exposure of negatively charged phospholipids; we speculate that the Rim101 pathway recognizes the surface charges.
生物膜由脂质双层组成。质膜的两个小叶之间的脂质组成不同,产生脂质不对称性。维持适当的脂质不对称性在生理上非常重要,其崩溃会引发包括细胞凋亡和血小板凝血在内的多种细胞反应。因此,脂质不对称性的变化必须得到恢复以维持“脂质不对称性稳态”。然而,迄今为止,尚未鉴定出脂质不对称性传感蛋白或任何相关的下游信号通路。我们最近证明,当甘油磷脂不对称性改变时,推定的酵母鞘脂长链碱转运体/转位酶Rsb1的表达会被诱导。通过突变体筛选,我们确定pH响应性Rim101途径、蛋白激酶Mck1和转录因子Mot3都参与脂质不对称性信号传导,并且Rim101途径在脂质不对称性变化时被激活。活化的转录因子Rim101通过抑制另一种转录阻遏物Nrg1来诱导Rsb1表达。脂质不对称性的变化伴随着带负电荷的磷脂在细胞表面的暴露;我们推测Rim101途径识别表面电荷。