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Phosphatidylserine synthesis at membrane contact sites promotes its transport out of the ER

机译:膜接触位点的磷脂酰丝氨酸合成促进其转运出ER

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摘要

Close contacts between organelles, often called membrane contact sites (MCSs), are regions where lipids are exchanged between organelles. Here, we identify a novel mechanism by which cells promote phospholipid exchange at MCSs. Previous studies have shown that phosphatidylserine (PS) synthase activity is highly enriched in portions of the endoplasmic reticulum (ER) in contact with mitochondria. The objective of this study was to determine whether this enrichment promotes PS transport out of the ER. We found that PS transport to mitochondria was more efficient when PS synthase was fused to a protein in the ER at ER-mitochondria contacts than when it was fused to a protein in all portions of the ER. Inefficient PS transport to mitochondria was corrected by increasing tethering between these organelles. PS transport to endosomes was similarly enhanced by PS production in regions of the ER in contact with endosomes. Together, these findings indicate that PS production at MCSs promotes PS transport out of the ER and suggest that phospholipid production at MCSs may be a general mechanism of channeling lipids to specific cellular compartments.
机译:细胞器之间的紧密接触(通常称为膜接触位点(MCS))是细胞器之间脂质交换的区域。在这里,我们确定了一种新的机制,通过该机制细胞可以促进MCS处的磷脂交换。先前的研究表明,磷脂酰丝氨酸(PS)合酶活性在与线粒体接触的内质网(ER)部分中高度富集。这项研究的目的是确定这种富集是否促进PS转运出ER。我们发现,当PS合酶在ER-线粒体接触处融合到ER中的蛋白质时,PS转运到线粒体比融合到ER所有部分中的蛋白质时更有效。通过增加这些细胞器之间的束缚,纠正了PS向线粒体的低效率转运。通过在与内体接触的ER区域中产生PS,类似地增强了向内体的PS运输。总之,这些发现表明,MCS处的PS产生促进PS转运出ER,并表明MCS处的磷脂产生可能是将脂质引导至特定细胞区室的一般机制。

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