Phosphatidylinositol-Phosphatidic Acid Exchange by Nir2 at ER-PM Contact Sites Maintains Phosphoinositide Signaling Competence

被引:178
作者
Kim, Yeun Ju [1 ]
Guzman-Hernandez, Maria-Luisa [1 ]
Wisniewski, Eva [1 ]
Balla, Tamas [1 ]
机构
[1] Eunice Kennedy Shriver Natl Inst Child Hlth & Hum, Sect Mol Signal Transduct, Program Dev Neurosci, NIH, Bethesda, MD 20892 USA
关键词
RETINAL-DEGENERATION-B; TRANSFER PROTEIN; ENDOPLASMIC-RETICULUM; ERYTHROCYTE-MEMBRANES; LIPID TRANSFER; INOSITOL; CELLS; DOMAINS; BRAIN; RDGB;
D O I
10.1016/j.devcel.2015.04.028
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Sustained agonist-induced production of the second messengers InsP(3) and diacylglycerol requires steady delivery of phosphatidylinositol (PtdIns) from its site of synthesis in the ER to the plasma membrane (PM) to maintain PtdIns(4,5)P-2 levels. Similarly, phosphatidic acid (PtdOH), generated from diacylglycerol in the PM, has to reach the ER for PtdIns resynthesis. Here, we show that the Drosophila RdgB homolog, Nir2, a presumed PtdIns transfer protein, not only transfers PtdIns from the ER to the PM but also transfers PtdOH to the opposite direction at ER-PM contact sites. PtdOH delivery to the ER is impaired in Nir2-depleted cells, leading to limited PtdIns synthesis and ultimately to loss of signaling from phospholipase C-coupled receptors. These studies reveal a unique feature of Nir2, namely its ability to serve as a highly localized lipid exchanger that ensures that PtdIns synthesis is matched with PtdIns(4,5)P-2 utilization so that cells maintain their signaling competence.
引用
收藏
页码:549 / 561
页数:13
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