Induction of Angiogenesis by a Fragment of Human Tyrosyl-tRNA Synthetase

The first step of protein synthesis is catalyzed by aminoacyl-tRNA synthetases. In addition, certain mammalian tRNA synthetases link protein synthesis to cytokine signaling pathways. In particular, human tyrosyl-tRNA synthetase (TyrRS) can be split by proteolysis into two fragments having distinct c...

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Veröffentlicht in:The Journal of biological chemistry 2002-06, Vol.277 (23), p.20124-20126
Hauptverfasser: Wakasugi, Keisuke, Slike, Bonnie M., Hood, John, Ewalt, Karla L., Cheresh, David A., Schimmel, Paul
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Sprache:eng
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Zusammenfassung:The first step of protein synthesis is catalyzed by aminoacyl-tRNA synthetases. In addition, certain mammalian tRNA synthetases link protein synthesis to cytokine signaling pathways. In particular, human tyrosyl-tRNA synthetase (TyrRS) can be split by proteolysis into two fragments having distinct cytokine activities. One of the TyrRS fragments (mini TyrRS) contains features identical to those in CXC chemokines (like interleukin-8) that also act as angiogenic factors. Here mini TyrRS (but not full-length TyrRS) is shown to stimulate chemotaxis of endothelial cells in vitro and stimulate angiogenesis in each of two in vivo animal models. The angiogenic activity of mini TyrRS can be opposed by anti-angiogenic chemokines like IP-10. Thus, a biological fragment of human tyrosyl-tRNA synthetase links protein synthesis to regulation of angiogenesis.
ISSN:0021-9258
1083-351X
DOI:10.1074/jbc.C200126200