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免疫抑制剂FTY720由2型鞘氨醇激酶磷酸化。

The immunosuppressant FTY720 is phosphorylated by sphingosine kinase type 2.

作者信息

Paugh Steven W, Payne Shawn G, Barbour Suzanne E, Milstien Sheldon, Spiegel Sarah

机构信息

Department of Biochemistry, Virginia Commonwealth University School of Medicine, Richmond, VA 23298, USA.

出版信息

FEBS Lett. 2003 Nov 6;554(1-2):189-93. doi: 10.1016/s0014-5793(03)01168-2.

Abstract

The potent immunosuppressive drug FTY720, a sphingosine analog, induces redistribution of lymphocytes from circulation to secondary lymphoid tissues. FTY720 is phosphorylated in vivo and functions as an agonist for four G-protein-coupled sphingosine-1-phosphate receptors. The identity of the kinase that phosphorylates FTY720 is still not known. Here we report that although both sphingosine kinase type 1 (SphK1) and type 2 (SphK2) can phosphorylate FTY720 with low efficiency, SphK2 is much more effective than SphK1. FTY720 inhibited phosphorylation of sphingosine catalyzed by SphK2 to a greater extent than it inhibits SphK1. Thus, SphK2 may be the relevant enzyme that is responsible for in vivo phosphorylation of FTY720.

摘要

强效免疫抑制药物FTY720是一种鞘氨醇类似物,可诱导淋巴细胞从循环系统重新分布至二级淋巴组织。FTY720在体内被磷酸化,并作为四种G蛋白偶联鞘氨醇-1-磷酸受体的激动剂发挥作用。使FTY720磷酸化的激酶的身份仍不清楚。在此我们报告,虽然1型鞘氨醇激酶(SphK1)和2型鞘氨醇激酶(SphK2)都能低效地使FTY720磷酸化,但SphK2比SphK1有效得多。FTY720对SphK2催化的鞘氨醇磷酸化的抑制程度大于对SphK1的抑制。因此,SphK2可能是负责FTY720体内磷酸化的相关酶。

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