Division of Hematology, Oncology and Transplantation, Vascular Biology Center, University of Minnesota, Minneapolis, MN;
Blood. 2014 Jan 16;123(3):377-90. doi: 10.1182/blood-2013-04-495887. Epub 2013 Nov 25.
Treatment of sickle cell disease (SCD) is hampered by incomplete understanding of pathways linking hemolysis to vaso-occlusion. We investigated these pathways in transgenic sickle mice. Infusion of hemoglobin or heme triggered vaso-occlusion in sickle, but not normal, mice. Methemoglobin, but not heme-stabilized cyanomethemoglobin, induced vaso-occlusion, indicating heme liberation is necessary. In corroboration, hemoglobin-induced vaso-occlusion was blocked by the methemoglobin reducing agent methylene blue, haptoglobin, or the heme-binding protein hemopexin. Untreated HbSS mice, but not HbAA mice, exhibited ∼10% vaso-occlusion in steady state that was inhibited by haptoglobin or hemopexin infusion. Antibody blockade of adhesion molecules P-selectin, von Willebrand factor (VWF), E-selectin, vascular cell adhesion molecule 1, intercellular adhesion molecule 1, platelet endothelial cell (EC) adhesion molecule 1, α4β1, or αVβ3 integrin prevented vaso-occlusion. Heme rapidly (5 minutes) mobilized Weibel-Palade body (WPB) P-selectin and VWF onto EC and vessel wall surfaces and activated EC nuclear factor κB (NF-κB). This was mediated by TLR4 as TAK-242 blocked WPB degranulation, NF-κB activation, vaso-occlusion, leukocyte rolling/adhesion, and heme lethality. TLR4(-/-) mice transplanted with TLR4(+/+) sickle bone marrow exhibited no heme-induced vaso-occlusion. The TLR4 agonist lipopolysaccharide (LPS) activated ECs and triggered vaso-occlusion that was inhibited by TAK-242, linking hemolysis- and infection-induced vaso-occlusive crises to TLR4 signaling. Heme and LPS failed to activate VWF and NF-κB in TLR4(-/-) ECs. Anti-LPS immunoglobulin G blocked LPS-induced, but not heme-induced, vaso-occlusion, illustrating LPS-independent TLR4 signaling by heme. Inhibition of protein kinase C, NADPH oxidase, or antioxidant treatment blocked heme-mediated stasis, WPB degranulation, and oxidant production. We conclude that intravascular hemolysis in SCD releases heme that activates endothelial TLR4 signaling leading to WPB degranulation, NF-κB activation, and vaso-occlusion.
镰状细胞病(SCD)的治疗受到对将溶血与血管阻塞联系起来的途径的不完全理解的阻碍。我们在转基因镰状细胞小鼠中研究了这些途径。血红蛋白或血红素的输注在镰状细胞但不在正常小鼠中引发血管阻塞。高铁血红蛋白,但不是血红素稳定的氰高铁血红蛋白,诱导血管阻塞,表明血红素释放是必要的。作为佐证,高铁血红蛋白还原剂亚甲蓝、触珠蛋白或血红素结合蛋白转铁蛋白阻断了血红蛋白诱导的血管阻塞。未经处理的 HbSS 小鼠,但不是 HbAA 小鼠,在稳态下表现出约 10%的血管阻塞,该阻塞被触珠蛋白或转铁蛋白输注抑制。粘附分子 P-选择素、血管性血友病因子 (VWF)、E-选择素、血管细胞粘附分子 1、细胞间粘附分子 1、血小板内皮细胞 (EC) 粘附分子 1、α4β1 或 αVβ3 整联蛋白的抗体阻断防止了血管阻塞。血红素迅速(5 分钟)将 Weibel-Palade 体 (WPB) P-选择素和 VWF 动员到 EC 和血管壁表面,并激活 EC 核因子 κB (NF-κB)。这是由 TLR4 介导的,因为 TAK-242 阻断了 WPB 脱颗粒、NF-κB 激活、血管阻塞、白细胞滚动/粘附和血红素致死。移植有 TLR4(+/+)镰状骨髓的 TLR4(-/-)小鼠没有表现出血红素诱导的血管阻塞。TLR4 激动剂脂多糖 (LPS) 激活 EC 并引发血管阻塞,该阻塞被 TAK-242 抑制,将溶血和感染引起的血管阻塞性危象与 TLR4 信号联系起来。血红素和 LPS 未能激活 TLR4(-/-)EC 中的 VWF 和 NF-κB。抗 LPS 免疫球蛋白 G 阻断了 LPS 诱导的,但不是血红素诱导的血管阻塞,说明了血红素通过 TLR4 信号诱导的 LPS 独立信号。蛋白激酶 C、NADPH 氧化酶或抗氧化剂治疗的抑制阻断了血红素介导的停滞、WPB 脱颗粒和氧化剂的产生。我们得出的结论是,SCD 中的血管内溶血释放血红素,血红素激活内皮 TLR4 信号导致 WPB 脱颗粒、NF-κB 激活和血管阻塞。