Doyle Colleen P, Rectenwald Andrew, Timple Liz, Hammond Gerald R V
Department of Cell Biology, University of Pittsburgh School of Medicine, Pittsburgh, PA 15261.
bioRxiv. 2024 Jan 11:2023.08.28.555163. doi: 10.1101/2023.08.28.555163.
Oxysterol binding protein (OSBP)-related proteins (ORPs) 5 and 8 have been shown to deplete the lipid phosphatidylinositol 4-phosphate (PI4P) at sites of membrane contact between the endoplasmic reticulum (ER) and plasma membrane (PM). This is believed to be caused by transport of PI4P from the PM to the ER, where PI4P is degraded by an ER-localized SAC1 phosphatase. This is proposed to power the anti-port of phosphatidylserine (PS) lipids from ER to PM, up their concentration gradient. Alternatively, ORPs have been proposed to sequester PI4P, dependent on the concentration of their alternative lipid ligand. Here, we aimed to distinguish these possibilities in living cells by orthogonal targeting of PI4P transfer and degradation to PM-mitochondria contact sites. Surprisingly, we found that orthogonal targeting of SAC1 to mitochondria enhanced PM PI4P turnover independent of targeting to contact sites with the PM. This turnover could be slowed by knock-down of soluble ORP2, which also has a major impact on PM PI4P levels even without SAC1 over-expression. The data reveal a role for contact site-independent modulation of PM PI4P levels and lipid antiport.
氧化甾醇结合蛋白(OSBP)相关蛋白(ORPs)5和8已被证明在内质网(ER)与质膜(PM)之间的膜接触位点消耗脂质磷脂酰肌醇4-磷酸(PI4P)。据信这是由于PI4P从质膜转运到内质网所致,在内质网中PI4P被内质网定位的SAC1磷酸酶降解。这被认为是驱动磷脂酰丝氨酸(PS)脂质从内质网到质膜的反向转运,逆其浓度梯度进行。另外,有人提出ORPs会根据其替代脂质配体的浓度螯合PI4P。在这里,我们旨在通过将PI4P转移和降解正交靶向到质膜 - 线粒体接触位点来区分活细胞中的这些可能性。令人惊讶的是,我们发现将SAC1正交靶向到线粒体可增强质膜PI4P的周转,而与靶向到与质膜的接触位点无关。这种周转可以通过敲低可溶性ORP2来减缓,即使没有SAC1过表达,ORP2对质膜PI4P水平也有重大影响。数据揭示了接触位点非依赖性调节质膜PI4P水平和脂质反向转运的作用。