Adamiak Mateusz, Chelvarajan Lakshman, Lynch Kevin R, Santos Webster L, Abdel-Latif Ahmed, Ratajczak Mariusz Z
Stem Cell Institute at James Graham Brown Cancer Center, University of Louisville, Louisville, KY, USA.
Department of Regenerative Medicine, Warsaw Medical University, Warsaw, Poland.
Oncotarget. 2017 Jul 24;8(39):65588-65600. doi: 10.18632/oncotarget.19514. eCollection 2017 Sep 12.
Sphingosine-1-phosphate (S1P) is a bioactive lipid involved in cell signaling and, if released from cells, also plays a crucial role in regulating the trafficking of lympho-hematopoietic cells, including primitive hematopoietic stem/progenitor cells (HSPCs). It has been demonstrated that S1P chemoattracts HSPCs, and its level in peripheral blood creates a gradient directing egress of these cells during mobilization. In this paper we analyzed hematopoiesis in mice deficient in sphingosine kinase 2 (Sphk2-KO mice) and studied the effect of this mutation on plasma S1P levels. We found that Sphk2-KO mice have normal hematopoiesis, and, in contrast to Sphk1-KO mice, the circulating S1P level is highly elevated in these animals and correlates with the fact that HSPCs in Sphk2-KO animals, also in contrast to Sphk1-KO animals, show enhanced mobilization. These results were recapitulated in wild type (WT) animals employing an Sphk2 inhibitor. We also administered an inhibitor of the S1P-degrading enzyme S1P lyase, known as tetrahydroxybutylimidazole (THI), to WT mice and observed that this resulted in an increase in S1P level in PB and enhanced mobilization of HSPCs. In sum, our results support a crucial role for S1P gradients in blood plasma in the mobilization process and indicate that small-molecule inhibitors of Sphk2 and Sgpl1 could be employed as mobilization-facilitating compounds. At the same time, further studies are needed to explain the unexpected effect of Sphk2 inhibition on increasing S1P levels in plasma.
鞘氨醇-1-磷酸(S1P)是一种参与细胞信号传导的生物活性脂质,如果从细胞中释放出来,它在调节淋巴细胞和造血细胞(包括原始造血干细胞/祖细胞(HSPCs))的运输过程中也起着至关重要的作用。已经证明,S1P对HSPCs具有化学趋化作用,其在外周血中的水平会形成一个梯度,在动员过程中引导这些细胞流出。在本文中,我们分析了鞘氨醇激酶2缺陷小鼠(Sphk2基因敲除小鼠)的造血情况,并研究了这种突变对血浆S1P水平的影响。我们发现,Sphk2基因敲除小鼠具有正常的造血功能,与Sphk1基因敲除小鼠不同的是,这些动物的循环S1P水平显著升高,这与Sphk2基因敲除动物中的HSPCs(同样与Sphk1基因敲除动物不同)表现出增强的动员能力这一事实相关。在使用Sphk2抑制剂的野生型(WT)动物中也重现了这些结果。我们还向WT小鼠施用了一种名为四羟基丁基咪唑(THI)的S1P降解酶S1P裂解酶的抑制剂,并观察到这导致外周血中S1P水平升高以及HSPCs的动员增强。总之,我们的结果支持血浆中S1P梯度在动员过程中起关键作用,并表明Sphk2和Sgpl1的小分子抑制剂可作为促进动员的化合物。同时,需要进一步研究来解释Sphk2抑制对血浆中S1P水平升高的意外影响。