Tumstatin, an endothelial cell-specific inhibitor of protein synthesis

被引:348
作者
Maeshima, Y
Sudhakar, A
Lively, JC
Ueki, K
Kharbanda, S
Kahn, CR
Sonenberg, N
Hynes, RO
Kalluri, R [1 ]
机构
[1] Beth Israel Deaconess Med Ctr, Dept Med, Program Matrix Biol, Boston, MA 02215 USA
[2] Beth Israel Deaconess Med Ctr, Ctr Canc, Boston, MA 02215 USA
[3] Harvard Univ, Sch Med, Boston, MA 02215 USA
[4] MIT, Ctr Canc Res, Howard Hughes Med Inst, Dept Biol, Cambridge, MA 02139 USA
[5] Joslin Diabet Ctr, Boston, MA 02215 USA
[6] Harvard Univ, Sch Med, Dana Farber Canc Inst, Div Canc Pharmacol, Boston, MA 02215 USA
[7] McGill Univ, Dept Biochem, Montreal, PQ H3G 1V6, Canada
[8] McGill Univ, McGill Canc Ctr, Montreal, PQ H3G 1V6, Canada
关键词
D O I
10.1126/science.1065298
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
Tumstatin is a 28-kilodalton fragment of type IV collagen that displays both anti-angiogenic and proapoptotic activity. Here we show that tumstatin functions as an endothelial cell-specific inhibitor of protein synthesis. Through a requisite interaction with alphaV beta3 integrin, tumstatin inhibits activation of focal adhesion kinase (FAK), phosphatidylinositol 3-kinase (PI3-kinase), protein kinase B (PKB/Akt), and mammalian target of rapamycin (mTOR), and it prevents the dissociation of eukaryotic initiation factor 4E protein (eIF4E) from 4E-binding protein 1. These results establish a rote for integrins in mediating ceti-specific inhibition of cap-dependent protein synthesis and suggest a potential mechanism for tumstatin's selective effects on endothelial cells.
引用
收藏
页码:140 / 143
页数:4
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