Promotion of the uptake of PS liposomes and apoptotic cells by a product of growth arrest-specific gene, gas6

被引:179
作者
Ishimoto, Y
Ohashi, K
Mizuno, K
Nakano, T
机构
[1] Shionogi & Co Ltd, Discovery Res Labs, Fukushima Ku, Osaka 5530002, Japan
[2] Tohoku Univ, Grad Sch Sci, Inst Biol, Aoba Ku, Sendai, Miyagi 9808578, Japan
关键词
Axl; Gas6; macrophage; phagocytosis; phosphatidylserine;
D O I
10.1093/oxfordjournals.jbchem.a022622
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
Gas6, a ligand of receptor tyrosine kinases Axl, Sky, and Mer, potentiates cell proliferation and prevents cell death, It also contains gamma-carboxylglutamic acid residues that mediate the interaction of some blood coagulation factors with negatively charged phospholipids, In our previous study, we demonstrated that Gas6 specifically binds to phosphatidylserine (PS) and links Art-expressing cells to the PS-coated surface, In this study, to further understand the biological role of the interaction of Gas6 with PS, we examined the effect of Grass on the uptake of PS liposomes by macrophages, In vitro phagocytosis studies showed that Gas6 enhanced the uptake of PS liposomes approximately threefold and that the interaction of Gas6 with the surface of macrophages was essential for this enhancement, Analyses of the mechanism of the uptake of PS liposome suggested that Gas6 interacts with PS liposome via its N-terminal Gla domain and with macrophages via its C-terminal domain, Like that of PS liposomes, the uptake of apoptotic cells by macrophages was also enhanced, approximately twofold, in the presence of Gas6, These findings suggest that Gas6 may help phagocytic cells recognize cells with PS exposed on their surfaces, which is considered to be one of the mechanisms for clearing away dying cells, Thus, Gas6 may play a critical role in homeostasis by facilitating the clearance of PS-expressing cells.
引用
收藏
页码:411 / 417
页数:7
相关论文
共 31 条
[1]  
ARITA H, 1991, J BIOL CHEM, V266, P19139
[2]   Immune clearance of phosphatidylserine-expressing cells by phagocytes -: The role of β2-glycoprotein I in macrophage recognition [J].
Balasubramanian, K ;
Chandra, J ;
Schroit, AJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (49) :31113-31117
[3]  
CONNOR J, 1994, J BIOL CHEM, V269, P2399
[4]   Human CD14 mediates recognition and phagocytosis of apoptotic cells [J].
Devitt, A ;
Moffatt, OD ;
Raykundalia, C ;
Capra, JD ;
Simmons, DL ;
Gregory, CD .
NATURE, 1998, 392 (6675) :505-509
[5]  
FADOK VA, 1992, J IMMUNOL, V148, P2207
[6]   RECOGNITION OF APOPTOTIC CELLS BY HUMAN MACROPHAGES - INHIBITION BY A MONOCYTE/MACROPHAGE-SPECIFIC MONOCLONAL-ANTIBODY [J].
FLORA, PK ;
GREGORY, CD .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1994, 24 (11) :2625-2632
[7]   SRB1, a class B scavenger receptor, recognizes both negatively charged liposomes and apoptotic cells [J].
Fukasawa, M ;
Adachi, H ;
Hirota, K ;
Tsujimoto, M ;
Arai, H ;
Inoue, K .
EXPERIMENTAL CELL RESEARCH, 1996, 222 (01) :246-250
[8]   THE MOLECULAR-BASIS OF BLOOD-COAGULATION [J].
FURIE, B ;
FURIE, BC .
CELL, 1988, 53 (04) :505-518
[9]   REEVALUATION OF THE ROLES OF PROTEIN-S AND GAS6 AS LIGANDS FOR THE RECEPTOR TYROSINE KINASE RSE/TYRO-3 [J].
GODOWSKI, PJ ;
MARK, MR ;
CHEN, JA ;
SADICK, MD ;
RAAB, H ;
HAMMOND, RG .
CELL, 1995, 82 (03) :355-358
[10]  
Goruppi S, 1996, ONCOGENE, V12, P471