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铁过载对骨髓损伤小鼠造血功能的作用及机制研究 被引量:5

Effects and mechanism of iron overload on hematopoiesis in mice with bone marrow injury
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摘要 目的 探讨铁过载对骨髓损伤小鼠造血功能的作用及可能机制.方法 将20只C57BL/6雄性小鼠随机分为对照组、铁剂组、照射组、照射+铁剂组,每组5只.通过给予小鼠4Gyγ射线照射及腹腔注射右旋糖酐铁建立骨髓损伤小鼠铁过载模型,观察各组小鼠铁负荷情况及骨髓单个核细胞(BMMNC)内可变铁池水平,检测各组小鼠外周血常规的改变;检测BMMNC数,红系、粒-单核系细胞比例及造血干/祖细胞功能改变;分析骨髓细胞,红系和粒-单核系细胞活性氧物质(ROS)水平.结果 ①骨髓活检及流式细胞术检测均显示发生铁过载.②与对照组相比,照射组小鼠血小板计数显著降低[(801.9±81.2)×10^9/L对(926.0±28.2)×10^9/L],BMMNC数及红系、粒-单核系细胞比例明显降低,骨髓造血集落形成单位(CFU)数和造血干细胞单克隆培养数明显减少(P值均<0.05).③与照射组相比,照射+铁剂组小鼠血小板计数显著降低[(619.0±60.9)×10^9/L对(801.9±81.2)×10^9/L],红系、粒-单核系细胞比例明显降低,骨髓造血CFU数和造血干细胞单克隆形成数明显减少(P值均<0.05).④照射+铁剂组BMMNC、红系和粒-单核系细胞ROS水平较照射组分别升高1.94、1.93和2.70倍(P值均< 0.05).结论 4Gyγ射线照射可造成小鼠骨髓损伤,在骨髓损伤基础上发生铁过载会加重损伤造血干/祖细胞功能,进一步研究发现可能由铁过载引起BMMNC内ROS水平升高所致. Objective To explore effects of iron overload on hematopoiesis in mice with bone marrow injury and its possible mechanism(s).Methods C57BL/6 mice were divided into control,iron,irradiation,irradiation+iron groups.The iron-overloaded model of bone marrow injury was set up after mice were exposed to the dose of 4 Gy total body irradiation and (or) were injected iron dextran intraperitoneally.Iron overload was confirmed by observing iron deposits in mice and bone marrow labile iron pool.Additionally,the number of peripheral blood and bone marrow mononuclear cells and the frequency of erythroid cells and myeloid cells were counted and hematopoietic function was assessed.Results ①Iron overload occurred by bone marrow biopsy and flow cytometry analysis.②Compared with control group,the number ofplatelets [(801.9±81.2) × 10^9/L vs (926.0±28.2) × 10^9/L] and BMMNC and the frequency of erythroid cells and myeloid cells decreased.Moreover,hematopoietic colony forming units and single-cell cloning counts decreased significantly in irradiation group (P 〈 0.05).③Compared with irradiation group,the number of platelets [(619.0±60.9) × 10^9/L vs (801.9±81.2) × 10^9/L] and the frequency of erythroid cells and myeloid cells decreased; moreover,hematopoietic colony forming units and singlecell cloning counts decreased significantly in irradiation + iron group (P〈0.05).④Compared with irradiation group,ROS level increased by 1.94 fold in BMMNC,1.93 fold in erythroid cells and 2.70 fold in myeloid cells,respectively (P 〈 0.05).Conclusions The dose of 4 Gy total body irradiation caused bone marrow damage and iron overload based on this injury model,which could damage bone marrow hematopoietic function aggravatingly.And further study found that iron overload was closely related to increased ROS level in BMMNC.The findings would be helpful to further study the injury mechanism of iron overload on the hematopoiesis of bone marrow.
出处 《中华血液学杂志》 CAS CSCD 北大核心 2014年第11期1000-1004,共5页 Chinese Journal of Hematology
基金 国家自然科学基金(81041043) 天津市自然科学基金(13JCYBJC23400) 天津市卫生局科技基金攻关项目及重点项目(13KG106、2013KR07) 天津市“131”创新型人才基金
关键词 铁超负荷 活性氧 造血干细胞 可变铁池 骨髓损伤 Iron overload Reactive oxygen species Hematopoietic stem cell Labile iron pool Bone marrow injury
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参考文献9

  • 1柴笑,赵明峰,李德冠,孟娟霞,卢文艺,穆娟,孟爱民.小鼠铁过载模型的建立及其对骨髓造血功能的影响[J].中国医学科学院学报,2013,35(5):547-552. 被引量:14
  • 2柴笑,赵明峰.铁过载在血液系统疾病中的危害及治疗进展[J].中华内科杂志,2013,52(5):431-433. 被引量:12
  • 3Lu W, Zhao M, Rajbhandary S, et al. Free iron catalyzes oxidative damage to hematopoietic cells/mesenchymal stem cells in vitro and suppresses hematopoiesis in iron overload patients[J]. Eur J Haematol, 2013, 91 (3):249-261.
  • 4Oliva EN, Ronco F, Marino A, et al. Iron chelation therapy asso- ciated with improvement of hematopoiesis in transfusion-depen- dent patients [ J ] .Transfusion, 2010, 50 ( 7 ): 1568-1570.
  • 5Hartmann J, Braulke F, Sinzig U, et al. Iron overload impairs proliferation of erythroid progenitors cells (BFU-E) from patients with myelodysplastic syndromes [J]. Leuk Res, 2013, 37 (3): 327-332.
  • 6Li D, Wang Y, Wu H, et al. Mitigation of ionizing radiation- induced bone marrow suppression by p38 inhibition and G-CSF administration[J]. J Radiat Res, 2011, 52(6):712-716.
  • 7Prus E, Fibach E. Flow cytometry measurement of the labile iron pool in human hematopoietic cells [J].Cytometry A, 2008, 73 ( 1 ):22-27.
  • 8谢芳,赵明峰,朱海波,卢文艺,徐新女,肖霞,穆娟,刘鹏江,李玉明.氧化应激对铁过载造血干祖细胞造血功能的影响[J].中华医学杂志,2011,91(46):3284-3288. 被引量:12
  • 9Taoka K, Kumano K, Nakamura F, et al. The effect of iron over- load and chelation on erythroid differentiation[ J ]. Int J Hematol, 2012, 95(2):149-159.

二级参考文献34

  • 1朱航,罗海吉,邓红,雷蕾,张守华.高铁小鼠模型的构建及铁代谢相关指标的观察(英文)[J].中国组织工程研究与临床康复,2007,11(8):1593-1597. 被引量:6
  • 2Valko M,Morris H,Cronin MT.Metals,toxicity and oxidative stress.Curr Med Chem,2005,12:1161-1208.
  • 3Zhao MF,Xie F,Li YM,et al.Increased intracellular concentration of reactive oxygen species mediated the deficient hematopoiesis of iron overload bone marrow.Blood,2010,116:4247 a.
  • 4Matayatsuk C,Poljak A,Bustamante S,et al.Quantitative determination of ortho-and meta-tyrosine as biomarkers of protein oxidative damage in β-thalassemia.Redox Rep,2007,12:219-228.
  • 5Naka K,Muraguchi T,Hoshii T,et al.Regulation of reactive oxygen species and genomic stability in hematopoietic stem cells.Antioxidants Redox Signal,2008,10:1883-1894.
  • 6Ghoti H,Amer H,Winder A,et al.Oxidative stress in red blood cells,platelets and polymorphonuclear leukocytes from patients with myelodysplastic syndrome.Eur J Haematol,2007,79:463-467.
  • 7Peddie CM,Wolf CR,McLellan LI,et al.Oxidative DNA damage in CD34 + myelodysplastic cells is associated with intracellular redox changes and elevated plasma tumor necrosis factor-alpha concentration.Br J Haematol,1997,99:625-631.
  • 8Kong Y,Zhou S,Kihm AJ,et al.Loss of alpha-hemoglobinstabilizing protein impairs erythropoiesis and exacerbates betathalassemia.J Clin Invest,2004,114:1457-1466.
  • 9Ghaffari S.Oxidative stress in the regulation of normal and neoplastic hematopoiesis.Antioxid Redox Signal,2008,10:1923-1940.
  • 10Johnson RM,Goyette G Jr,Ravindranath Y,et al.Hemoglobin autoxidation and regulation of endogenous H202 levels in erythroeytes.Free Radic Biol Med,2005,39:1407-1417.

共引文献31

同被引文献61

  • 1范慧霞.中药丹参药理作用研究概况[J].新疆中医药,2007,25(5):113-117. 被引量:43
  • 2Lu WY, Zhao MF,Xie F, et al. Free iron catalyzes oxidative dam- age to hematopoietic cells/mesenchymal stem ceils in vitro and sup- presses hematopoiesis in iron overload patients [ J ]. Eur J Haema- tol, 2013,91 (3) : 249-261.
  • 3Hartmann J, Braulke F, Sinzig U, et al. Iron overload impairs pro- liferation of erythrold progenitors cells (BFU-E) from patients with myelodysplastic syndromes [ J 1. Leuk Res, 2013,37 (3) :327-332.
  • 4Oliva EN, Ronco F, Marino A, et al. Iron chelation therapy asso- ciated with improvement of hematopoiesis in transfusion-dependent patients [J]. Transfusion, 2010,50 (7) : 1568-1570.
  • 5S6nehez-GonzOlez PD, L6pez-Hernandez FJ, Morales AI, et al. Effects of deferasirox on renal function and renal epithelial cell death[ J~. Toxicol Lett, 2011,203 (2) : 154-161.
  • 6Chaudhary P, Pullarkat V. Deferasirox appraisal of safety and effi- cacy in long-term therapy[ J~. Blood Med,2013,5 (4) :101-110.
  • 7Zhao MF, Xie F, Li YM, et al. Increased intracellular concentra- tionof reactive oxygen species mediated the deficienthematopoiesis of iron overload bone marrow [ J ]. Blood, 2010,116 ( 11 ) :42 -47.
  • 8Taoka K, Kumano K, Nakamura F, et al. The effect of ironover- load and chelation onerythroid differentiation [ J ]. Int J Hematol, 2012,95 (2) : 149-159.
  • 9Guafiqlia R, Martorelli MC, Villani O, et al. Positive effecton hematopoiesis in patients with myelodysplasticsydromereceiving de- ferasirox as oral iron chelation therapy: a briefreview [ J ]. Leuk Res, 2011,35(5) :566-570.
  • 10ScottB,DeegHJ.Hemopoietic cell transplantation as curative therapy of myelodysplastic syndromes and myeloproliferative disorders[J].Best Pract Res Clin Haematol,2006,19(3):519-533.doi:10.1016/j.beha.2005.07.009.

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