Stem and Progenitor Cell Biology Program, Maine Medical Center Research Institute, Scarborough, ME, USA.
Blood. 2012 Jun 7;119(23):5522-31. doi: 10.1182/blood-2011-11-392571. Epub 2012 Apr 16.
Sprouty proteins are established modifiers of receptor tyrosine kinase (RTK) signaling and play important roles in vasculogenesis, bone morphogenesis, and renal uteric branching. Little is understood, however, concerning possible roles for these molecular adaptors during hematopoiesis. Within erythroid lineage, Spry1 was observed to be selectively and highly expressed at CFU-e to erythroblast stages. In analyses of possible functional roles, an Mx1-Cre approach was applied to conditionally delete Spry1. At steady state, Spry1 deletion selectively perturbed erythroid development and led to reticulocytosis plus heightened splenic erythropoiesis. When challenged by hemolysis, Spry1-null mice exhibited worsened anemia and delayed recovery. During short-term marrow transplantation, Spry1-null donor marrow also failed to efficiently rescue the erythron. In each anemia model, however, hyperexpansion of erythroid progenitors was observed. Spry function depends on phosphorylation of a conserved N-terminal PY motif. Through an LC-MS/MS approach, Spry1 was discovered to be regulated via the erythropoietin receptor (EPOR), with marked EPO-induced Spry1-PY53 phosphorylation observed. When EPOR signaling pathways were analyzed within Spry1-deficient erythroid progenitors, hyperactivation of not only Erk1,2 but also Jak2 was observed. Studies implicate Spry1 as a novel regulator of erythropoiesis during anemia, transducer of EPOR signals, and candidate suppressor of Jak2 activity.
芽蛋白是受体酪氨酸激酶 (RTK) 信号的既定调节剂,在血管生成、骨形态发生和肾输尿管分支中发挥重要作用。然而,对于这些分子接头在造血过程中可能发挥的作用,人们知之甚少。在红细胞谱系中,观察到 Spry1 在 CFU-e 到成红细胞阶段选择性和高度表达。在分析可能的功能作用时,应用 Mx1-Cre 方法条件性删除 Spry1。在稳定状态下,Spry1 的缺失选择性地扰乱了红细胞的发育,并导致网织红细胞增多和脾脏红细胞生成增加。当受到溶血的挑战时,Spry1 缺失的小鼠表现出更严重的贫血和恢复延迟。在短期骨髓移植中,Spry1 缺失的供体骨髓也未能有效地挽救红细胞系。然而,在每种贫血模型中,都观察到红细胞祖细胞的过度扩张。Spry 的功能依赖于保守的 N 端 PY 基序的磷酸化。通过 LC-MS/MS 方法,发现 Spry1 通过促红细胞生成素受体 (EPOR) 进行调节,观察到 EPO 诱导的 Spry1-PY53 磷酸化显著增加。当分析 Spry1 缺陷的红细胞祖细胞中的 EPOR 信号通路时,不仅观察到 Erk1,2 的过度激活,而且还观察到 Jak2 的过度激活。研究表明 Spry1 是贫血期间红细胞生成的新型调节剂、EPOR 信号的转导子和 Jak2 活性的候选抑制剂。