Carter C D, Schultz T W, McDonald T P
Department of Animal Science, College of Veterinary Medicine, University of Tennessee, Knoxville 37901-1071.
Radiat Res. 1993 Jul;135(1):32-9.
Previous work showed that treatment of irradiated mice with a thrombocytopoiesis-stimulating factor (TSF or thrombopoietin) decreased the degree and duration of thrombocytopenia in the period after irradiation. In an attempt to elucidate the radio-protective effects of TSF, femoral megakaryocyte sizes and numbers were measured in mice treated with 3.0 Gy of 137Cs gamma rays and TSF. For controls, other irradiated mice were given human serum albumin (HSA), the carrier protein for TSF, rabbit anti-mouse platelet serum (RAMPS), or normal rabbit serum (NRS); megakaryocyte sizes and numbers were studied on Days 7-14. The results showed that irradiated, TSF-treated mice had significantly larger megakaryocytes on all days assessed compared to HSA-treated control mice. Likewise, RAMPS-treated mice had significantly larger megakaryocytes 14 days after irradiation compared to NRS-treated mice. Megakaryocyte numbers were significantly depressed in TSF-treated mice on Days 7-10 and 14 and on Day 10 in RAMPS-treated mice, compared to their respective controls. Therefore, irradiated mice treated with TSF yielded results similar to RAMPS-treated mice. Megakaryocyte sizes and numbers were also determined for mice treated with 40,000 U/mouse of interleukin-6 (IL-6), 227 U/mouse of granulocyte-macrophage colony-stimulating factor (GM-CSF), or a combination of both cytokines; bovine serum albumin (BSA) was used as a control for these cytokine treatments. Unlike TSF treatment, GM-CSF significantly increased megakaryocyte numbers on both Days 10 and 14; the combination of both growth factors also increased megakaryocyte numbers on Day 14 compared to BSA-treated control mice. However, megakaryocyte size was decreased in GM-CSF-treated mice and in mice treated with both growth factors on Day 10. High levels of IL-6 failed to affect megakaryocyte size or number significantly on any day evaluated. The data of the present report, showing that TSF significantly increases megakaryocyte sizes and platelet counts of sublethally irradiated mice, indicate that thrombopoietin will be useful in treating patients undergoing bone marrow transplantation and/or patients with platelet production problems.
先前的研究表明,用血小板生成刺激因子(TSF或血小板生成素)治疗受辐照小鼠,可减轻辐照后一段时间内血小板减少的程度并缩短其持续时间。为了阐明TSF的辐射防护作用,对接受3.0 Gy 137Csγ射线和TSF治疗的小鼠测量了股骨巨核细胞的大小和数量。作为对照,给其他受辐照小鼠注射人血清白蛋白(HSA,TSF的载体蛋白)、兔抗小鼠血小板血清(RAMPS)或正常兔血清(NRS);在第7至14天研究巨核细胞的大小和数量。结果显示,与接受HSA治疗的对照小鼠相比,接受辐照并经TSF治疗的小鼠在所有评估天数的巨核细胞都明显更大。同样,与接受NRS治疗的小鼠相比,接受RAMPS治疗的小鼠在辐照后14天的巨核细胞明显更大。与各自的对照相比,接受TSF治疗的小鼠在第7至10天和第14天以及接受RAMPS治疗的小鼠在第10天的巨核细胞数量显著减少。因此,接受TSF治疗的辐照小鼠产生的结果与接受RAMPS治疗的小鼠相似。还对接受40,000 U/小鼠白细胞介素-6(IL-6)、227 U/小鼠粒细胞-巨噬细胞集落刺激因子(GM-CSF)或两种细胞因子联合治疗的小鼠测定了巨核细胞的大小和数量;牛血清白蛋白(BSA)用作这些细胞因子治疗的对照。与TSF治疗不同,GM-CSF在第10天和第14天都显著增加了巨核细胞数量;与接受BSA治疗的对照小鼠相比,两种生长因子联合使用在第14天也增加了巨核细胞数量。然而,接受GM-CSF治疗的小鼠以及在第10天接受两种生长因子治疗的小鼠的巨核细胞大小减小。在任何评估天数,高水平的IL-6均未显著影响巨核细胞的大小或数量。本报告的数据表明,TSF可显著增加亚致死剂量辐照小鼠的巨核细胞大小和血小板计数,这表明血小板生成素将有助于治疗接受骨髓移植的患者和/或有血小板生成问题的患者。