Department of Biological Sciences, Louisiana State University, Baton Rouge, LA 70803, USA.
J Neurophysiol. 2009 Dec;102(6):3295-309. doi: 10.1152/jn.00119.2009. Epub 2009 Sep 23.
Evidence is emerging indicating that sphingosine-1-phosphate (S1P) participates in signaling in the retina. To determine whether S1P might be involved in signaling in the inner retina specifically, we examine the effects of this sphingolipid on cultured retinal amacrine cells. Whole cell voltage-clamp recordings reveal that S1P activates a cation current that is dependent on signaling through G(i) and phospholipase C. These observations are consistent with the involvement of members of the S1P receptor family of G-protein-coupled receptors in the production of the current. Immunocytochemistry and PCR amplification provide evidence for the expression of S1P1R and S1P3R in amacrine cells. The receptor-mediated channel activity is shown to be highly sensitive to blockade by lanthanides consistent with the behavior of transient receptor potential canonical (TRPC) channels. PCR products amplified from amacrine cells reveal that TRPCs 1 and 3-7 channel subunits have the potential to be expressed. Because TRPC channels provide a Ca(2+) entry pathway, we asked whether S1P caused cytosolic Ca(2+) elevations in amacrine cells. We show that S1P-dependent Ca(2+) elevations do occur in these cells and that they might be mediated by S1P1R and S1P3R. The Ca(2+) elevations are partially due to release from internal stores, but the largest contribution is from influx across the plasma membrane. The effect of inhibition of sphingosine kinase suggests that the production of cytosolic S1P underlies the sustained nature of the Ca(2+) elevations. Elucidation of the downstream effects of these signals will provide clues to the role of S1P in regulating inner retinal function.
有证据表明,鞘氨醇-1-磷酸(S1P)参与视网膜信号转导。为了确定 S1P 是否可能参与特定的内视网膜信号转导,我们研究了这种鞘脂对内培养的视网膜无长突细胞的作用。全细胞膜片钳记录显示,S1P 激活依赖于 G(i)和磷脂酶 C 信号转导的阳离子电流。这些观察结果与 S1P 受体家族的 G 蛋白偶联受体成员参与电流产生一致。免疫细胞化学和 PCR 扩增为无长突细胞中 S1P1R 和 S1P3R 的表达提供了证据。受体介导的通道活性对镧系元素的阻断高度敏感,与瞬时受体电位经典(TRPC)通道的行为一致。从无长突细胞扩增的 PCR 产物表明,TRPCs 1 和 3-7 通道亚基有可能表达。由于 TRPC 通道提供了 Ca(2+)进入途径,我们询问 S1P 是否会导致无长突细胞中的细胞质 Ca(2+)升高。我们表明,S1P 依赖性 Ca(2+)升高确实发生在这些细胞中,并且它们可能由 S1P1R 和 S1P3R 介导。Ca(2+)升高部分是由于内部储存库的释放引起的,但最大的贡献来自质膜的流入。鞘氨醇激酶抑制的作用表明,细胞质 S1P 的产生是 Ca(2+)升高持续性质的基础。阐明这些信号的下游效应将为 S1P 在调节内视网膜功能中的作用提供线索。