Otsuka Hirotada, Takito Jiro, Endo Yasuo, Yagi Hideki, Soeta Satoshi, Yanagisawa Nobuaki, Nonaka Naoko, Nakamura Masanori
Department of Oral Anatomy and Developmental Biology, School of Dentistry, Showa University, 1-5-8 Hatanodai, Shinagawa-ku, Tokyo, 142-8555 Japan.
Division of Molecular Regulation, Graduate School of Dentistry, Tohoku University, 4-1 Seiryo-machi, Aoba-ku, Sendai, 980-8575 Japan.
BMC Hematol. 2016 Feb 11;16:4. doi: 10.1186/s12878-016-0041-0. eCollection 2016.
Mammalian erythropoiesis can be divided into two distinct types, primitive and definitive, in which new cells are derived from the yolk sac and hematopoietic stem cells, respectively. Primitive erythropoiesis occurs within a restricted period during embryogenesis. Primitive erythrocytes remain nucleated, and their hemoglobins are different from those in definitive erythrocytes. Embryonic type hemoglobin is expressed in adult animals under genetically abnormal condition, but its later expression has not been reported in genetically normal adult animals, even under anemic conditions. We previously reported that injecting animals with nitrogen-containing bisphosphonate (NBP) decreased erythropoiesis in bone marrow (BM). Here, we induced severe anemia in a mouse model by injecting NBP injection in combination with phenylhydrazine (PHZ), and then we analyzed erythropoiesis and the levels of different types of hemoglobin.
Splenectomized mice were treated with NBP to inhibit erythropoiesis in BM, and with PHZ to induce hemolytic anemia. We analyzed hematopoietic sites and peripheral blood using morphological and molecular biological methods.
Combined treatment of splenectomized mice with NBP and PHZ induced critical anemia compared to treatment with PHZ alone, and numerous nucleated erythrocytes appeared in the peripheral blood. In the BM, immature CD71-positive erythroblasts were increased, and extramedullary erythropoiesis occurred in the liver. Furthermore, embryonic type globin mRNA was detected in both the BM and the liver. In peripheral blood, spots that did not correspond to control hemoglobin were observed in 2D electrophoresis. ChIP analyses showed that KLF1 and KLF2 bind to the promoter regions of β-like globin. Wine-colored capsuled structures were unexpectedly observed in the abdominal cavity, and active erythropoiesis was also observed in these structures.
These results indicate that primitive erythropoiesis occurs in adult mice to rescue critical anemia because primitive erythropoiesis does not require macrophages as stroma whereas macrophages play a pivotal role in definitive erythropoiesis even outside the medulla. The cells expressing embryonic hemoglobin in this study were similar to primitive erythrocytes, indicating the possibility that yolk sac-derived primitive erythroid cells may persist into adulthood in mice.
哺乳动物的红细胞生成可分为两种不同类型,即原始型和定型型,新细胞分别来源于卵黄囊和造血干细胞。原始红细胞生成发生在胚胎发育的特定时期内。原始红细胞保留细胞核,其血红蛋白与定型红细胞中的血红蛋白不同。胚胎型血红蛋白在基因异常的成年动物中表达,但在基因正常的成年动物中,即使在贫血条件下,也未报道其后期表达情况。我们之前报道过,给动物注射含氮双膦酸盐(NBP)会减少骨髓(BM)中的红细胞生成。在此,我们通过联合注射NBP和苯肼(PHZ)在小鼠模型中诱导严重贫血,然后分析红细胞生成及不同类型血红蛋白的水平。
对脾切除的小鼠用NBP抑制骨髓中的红细胞生成,并用PHZ诱导溶血性贫血。我们使用形态学和分子生物学方法分析造血部位和外周血。
与单独使用PHZ治疗相比,联合使用NBP和PHZ治疗脾切除的小鼠会诱导严重贫血,外周血中出现大量有核红细胞。在骨髓中,未成熟的CD71阳性成红细胞增加,肝脏中发生了髓外红细胞生成。此外,在骨髓和肝脏中均检测到胚胎型珠蛋白mRNA。在外周血的二维电泳中观察到与对照血红蛋白不对应的斑点。染色质免疫沉淀分析表明,KLF1和KLF2与β样珠蛋白的启动子区域结合。在腹腔中意外观察到酒红色胶囊状结构,在这些结构中也观察到了活跃的红细胞生成。
这些结果表明,成年小鼠会发生原始红细胞生成以挽救严重贫血,因为原始红细胞生成不需要巨噬细胞作为基质,而定型红细胞生成即使在骨髓外巨噬细胞也起着关键作用。本研究中表达胚胎型血红蛋白的细胞类似于原始红细胞,这表明卵黄囊来源的原始红细胞可能在小鼠成年后持续存在。