机构:
CSIC, IIBB IDIBAPS, Inst Biomed Res Barcelona, Dept Cell Death & Proliferat, Barcelona 08036, SpainCSIC, IIBB IDIBAPS, Inst Biomed Res Barcelona, Dept Cell Death & Proliferat, Barcelona 08036, Spain
Bellido-Martin, Lola
[1
]
de Frutos, Pablo Garcia
论文数: 0引用数: 0
h-index: 0
机构:
CSIC, IIBB IDIBAPS, Inst Biomed Res Barcelona, Dept Cell Death & Proliferat, Barcelona 08036, SpainCSIC, IIBB IDIBAPS, Inst Biomed Res Barcelona, Dept Cell Death & Proliferat, Barcelona 08036, Spain
de Frutos, Pablo Garcia
[1
]
机构:
[1] CSIC, IIBB IDIBAPS, Inst Biomed Res Barcelona, Dept Cell Death & Proliferat, Barcelona 08036, Spain
来源:
VITAMIN K
|
2008年
/
78卷
关键词:
D O I:
10.1016/S0083-6729(07)00009-X
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 (growth arrest-specific gene 6) is the last addition to the family of plasma vitamin K-dependent proteins. Gas6 was cloned and characterized in 1993 and found to be similar to the plasma anticoagulant protein S. Soon after it was recognized as a growth factor-like molecule, as it interacted with receptor tyrosine kinases (RTKs) of the TAM family; Tyro3, Axl, and MerTK. Since then, the role of Gas6, protein S, and the TAM receptors has been found to be important in inflammation, hemostasis, and cancer, making this system an interesting target in biomedicine. Gas6 employs a unique mechanism of action, interacting through its vitamin K-dependent Gla module with phosphatidylserine-containing membranes and through its carboxy-terminal LG domains with the TAM membrane receptors. The fact that these proteins are affected by anti-vitamin K therapy is discussed in detail. (C) 2008 Elsevier Inc.