Sequential breakdown of 3-phosphorylated phosphoinositides is essential for the completion of macropinocytosis

被引:87
作者
Maekawa, Masashi [1 ,6 ]
Terasaka, Shimpei [1 ]
Mochizuki, Yasuhiro [3 ,5 ]
Kawai, Katsuhisa [4 ]
Ikeda, Yuka [4 ]
Araki, Nobukazu [4 ]
Skolnik, Edward Y.
Taguchi, Tomohiko [1 ,2 ]
Arai, Hiroyuki [1 ,2 ]
机构
[1] Univ Tokyo, Dept Hlth Chem, Grad Sch Pharmaceut Sci, Tokyo 1130033, Japan
[2] Univ Tokyo, Pathol Cell Biol Lab, Grad Sch Pharmaceut Sci, Tokyo 1130033, Japan
[3] Univ Tokyo, Dept Mol Biol & Med, Res Ctr Adv Sci & Technol, Tokyo 1538904, Japan
[4] Kagawa Univ, Dept Histol & Cell Biol, Sch Med, Miki, Kagawa 7610793, Japan
[5] NYU, Dept Pharmacol, Div Nephrol,Lagone Med Ctr, Helen L & Martin S Kimmel Ctr Biol & Med,Skirball, New York, NY 10016 USA
[6] St Michaels Hosp, Li Ka Shing Knowledge Inst, Keenan Res Ctr, Toronto, ON M5B 1W8, Canada
基金
日本科学技术振兴机构; 美国国家卫生研究院;
关键词
CLATHRIN-MEDIATED ENDOCYTOSIS; PLECKSTRIN-HOMOLOGY-DOMAIN; CA2+-ACTIVATED K+ CHANNEL; 4-PHOSPHATASE TYPE-II; PHOSPHATIDYLINOSITOL; 3-PHOSPHATE; PLASMA-MEMBRANE; MACROPINOSOME FORMATION; CAENORHABDITIS-ELEGANS; CELLULAR FUNCTIONS; CELLS;
D O I
10.1073/pnas.1311029111
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Macropinocytosis is a highly conserved endocytic process by which extracellular fluid and solutes are internalized into cells. Macropinocytosis starts with the formation of membrane ruffles at the plasma membrane and ends with their closure. The transient and sequential emergence of phosphoinositides PI(3,4,5)P-3 and PI(3,4)P-2 in the membrane ruffles is essential for macropinocytosis. By making use of information in the Caenorhabditis elegans mutants defective in fluid-phase endocytosis, we found that mammalian phosphoinositide phosphatase MTMR6 that dephosphorylates PI(3)P to PI, and its binding partner MTMR9, are required for macropinocytosis. INPP4B, which dephosphorylates PI(3,4)P-2 to PI(3)P, was also found to be essential for macropinocytosis. These phosphatases operate after the formation of membrane ruffles to complete macropinocytosis. Finally, we showed that KCa3.1, a Ca2+-activated K+ channel that is activated by PI(3)P, is required for macropinocytosis. We propose that the sequential breakdown of PI(3,4,5)P-3 -> PI(3,4)P-2 -> PI(3)P -> PI controls macropinocytosis through specific effectors of the intermediate phosphoinositides.
引用
收藏
页码:E978 / E987
页数:10
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