Sun Kaiqi, Zhang Yujin, Bogdanov Mikhail V, Wu Hongyu, Song Anren, Li Jessica, Dowhan William, Idowu Modupe, Juneja Harinder S, Molina Jose G, Blackburn Michael R, Kellems Rodney E, Xia Yang
Department of Biochemistry and Molecular Biology, Graduate School of Biomedical Science, and.
Department of Biochemistry and Molecular Biology.
Blood. 2015 Mar 5;125(10):1643-52. doi: 10.1182/blood-2014-08-595751. Epub 2015 Jan 13.
Erythrocyte possesses high sphingosine kinase 1 (SphK1) activity and is the major cell type supplying plasma sphingosine-1-phosphate, a signaling lipid regulating multiple physiological and pathological functions. Recent studies revealed that erythrocyte SphK1 activity is upregulated in sickle cell disease (SCD) and contributes to sickling and disease progression. However, how erythrocyte SphK1 activity is regulated remains unknown. Here we report that adenosine induces SphK1 activity in human and mouse sickle and normal erythrocytes in vitro. Next, using 4 adenosine receptor-deficient mice and pharmacological approaches, we determined that the A2B adenosine receptor (ADORA2B) is essential for adenosine-induced SphK1 activity in human and mouse normal and sickle erythrocytes in vitro. Subsequently, we provide in vivo genetic evidence that adenosine deaminase (ADA) deficiency leads to excess plasma adenosine and elevated erythrocyte SphK1 activity. Lowering adenosine by ADA enzyme therapy or genetic deletion of ADORA2B significantly reduced excess adenosine-induced erythrocyte SphK1 activity in ADA-deficient mice. Finally, we revealed that protein kinase A-mediated extracellular signal-regulated kinase 1/2 activation functioning downstream of ADORA2B underlies adenosine-induced erythrocyte SphK1 activity. Overall, our findings reveal a novel signaling network regulating erythrocyte SphK1 and highlight innovative mechanisms regulating SphK1 activity in normal and SCD.
红细胞具有较高的鞘氨醇激酶1(SphK1)活性,是提供血浆1-磷酸鞘氨醇的主要细胞类型,1-磷酸鞘氨醇是一种调节多种生理和病理功能的信号脂质。最近的研究表明,镰状细胞病(SCD)中红细胞SphK1活性上调,并促进镰状化和疾病进展。然而,红细胞SphK1活性是如何被调节的仍不清楚。在此我们报告,腺苷在体外可诱导人和小鼠镰状及正常红细胞中的SphK1活性。接下来,我们使用4种腺苷受体缺陷小鼠和药理学方法,确定A2B腺苷受体(ADORA2B)对于腺苷在体外诱导人和小鼠正常及镰状红细胞中的SphK1活性至关重要。随后,我们提供了体内遗传学证据,表明腺苷脱氨酶(ADA)缺乏会导致血浆腺苷过多和红细胞SphK1活性升高。通过ADA酶疗法或ADORA2B基因缺失降低腺苷,可显著降低ADA缺陷小鼠中过量腺苷诱导的红细胞SphK1活性。最后,我们揭示了ADORA2B下游的蛋白激酶A介导的细胞外信号调节激酶1/2激活是腺苷诱导红细胞SphK1活性的基础。总体而言,我们的研究结果揭示了一个调节红细胞SphK1的新型信号网络,并突出了在正常和SCD中调节SphK1活性的创新机制。