Regulation of Angiogenesis by Aminoacyl-tRNA Synthetases

被引:29
|
作者
Mirando, Adam C. [1 ]
Francklyn, Christopher S. [1 ]
Lounsbury, Karen M. [2 ]
机构
[1] Univ Vermont, Dept Biochem, Coll Med, Burlington, VT 05405 USA
[2] Univ Vermont, Coll Med, Dept Pharmacol, Burlington, VT 05405 USA
来源
关键词
angiogenesis; aminoacyl-tRNA synthetase; endothelial cells; non-canonical functions; ENDOTHELIAL GROWTH-FACTOR; NECROSIS-FACTOR-ALPHA; TRANSLATIONAL CONTROL; VASCULAR DEVELOPMENT; NONCANONICAL FUNCTION; FUNCTIONAL RECEPTOR; GAMMA-INTERFERON; CELL APOPTOSIS; CXC CHEMOKINES; ACTIVE-SITE;
D O I
10.3390/ijms151223725
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
In addition to their canonical roles in translation the aminoacyl-tRNA synthetases (ARSs) have developed secondary functions over the course of evolution. Many of these activities are associated with cellular survival and nutritional stress responses essential for homeostatic processes in higher eukaryotes. In particular, six ARSs and one associated factor have documented functions in angiogenesis. However, despite their connection to this process, the ARSs are mechanistically distinct and exhibit a range of positive or negative effects on aspects of endothelial cell migration, proliferation, and survival. This variability is achieved through the appearance of appended domains and interplay with inflammatory pathways not found in prokaryotic systems. Complete knowledge of the non-canonical functions of ARSs is necessary to understand the mechanisms underlying the physiological regulation of angiogenesis.
引用
收藏
页码:23725 / 23748
页数:24
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