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

被引:50
|
作者
Kannan, Muthukumar [1 ]
Lahiri, Sujoy [2 ]
Liu, Li-Ka [1 ]
Choudhary, Vineet [1 ]
Prinz, William A. [1 ]
机构
[1] NIDDK, Lab Cell & Mol Biol, NIH, Bethesda, MD 20892 USA
[2] Univ Virginia, Sch Med, Dept Pharmacol, Charlottesville, VA 22908 USA
关键词
endoplasmic reticulum; lipid transfer pro-teins; lipid biochemistry; mitochondria phospholipids/trafficking; lipid transport; phosphatidylethanolamine; phosphatidylserine synthase; MITOCHONDRIA-ASSOCIATED MEMBRANES; YEAST SACCHAROMYCES-CEREVISIAE; HAMSTER OVARY CELLS; ENDOPLASMIC-RETICULUM; PHOSPHOLIPID-SYNTHESIS; ESCHERICHIA-COLI; MAMMALIAN-CELLS; PLASMA-MEMBRANE; LIPID TRANSPORT; TRITON X-100;
D O I
10.1194/jlr.M072959
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
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.
引用
收藏
页码:553 / 562
页数:10
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