Sphingosine kinase 1 catalyzes the formation of sphingosine-1-phosphate, a lipid mediator involved in the regulation of angiogenesis. Sphingosine kinase 1 is constitutively released from cells, even though it lacks a classical signal peptide sequence. Because copper-dependent non-classical stress-induced release of FGF1 also regulates angiogenesis, we questioned whether sphingosine kinase 1 is involved in the FGF1 release pathway. We report that (i) the coexpression of sphingosine kinase 1 with FGF1 inhibited the release of sphingosine kinase 1 at 37 degrees C; (ii) sphingosine kinase 1 was released at 42 degrees C in complex with FGF1; (iii) sphingosine kinase 1 null cells failed to release FGF1 at stress; (iv) sphingosine kinase 1 is a high affinity copper-binding protein which formed a complex with FGF1 in a cell-free system, and (v) sphingosine kinase 1 over expression rescued the release of FGF1 from inhibition by the copper chelator, tetrathiomolybdate. We propose that sphingosine kinase 1 is a component of the copper-dependent FGF1 release pathway.

译文

:鞘氨醇激酶1催化鞘氨醇-1-磷酸的形成,一种参与调节血管生成的脂质介体。鞘氨醇激酶1从细胞组成性释放,即使它缺乏经典的信号肽序列。因为铜依赖性非经典应激诱导的FGF1释放也调节血管生成,所以我们质疑鞘氨醇激酶1是否参与FGF1释放途径。我们报告(i)鞘氨醇激酶1与FGF1的共表达抑制鞘氨醇激酶1在37摄氏度的释放; (ii)鞘氨醇激酶1在42℃下与FGF1复合释放; (iii)鞘氨醇激酶1无效细胞在压力下不能释放FGF1; (iv)鞘氨醇激酶1是一种高亲和力的铜结合蛋白,可在无细胞系统中与FGF1形成复合物;并且(v)鞘氨醇激酶1的过表达从铜螯合剂四硫代钼酸盐的抑制作用中拯救了FGF1的释放。我们建议鞘氨醇激酶1是铜依赖性FGF1释放途径的一个组成部分。

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