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不同来源间充质干细胞治疗小鼠放射性肺损伤的研究 被引量:2

Comparison of Mesenchymal Stem Cells Derived from Different Tis sues on Moderating Irradiation Induced Lung Injury
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摘要 目的:观察小鼠骨髓、肺及胚胎背主动脉区来源的间充质干细胞(MSC)对小鼠肺损伤的治疗作用。方法:将小鼠随机分为5组,即正常组、单纯照射组、OP9细胞治疗组、胚肺MSC治疗组、胚胎背主动脉区来源MSC治疗组(DA组),分别将OP9细胞、胚肺和DA区MSC移植入受体小鼠,4、9、13、17、23周后观察各组小鼠外观、肺组织的病理变化。结果:小鼠外观评分均值由高到低顺序为正常组、DA组、胚肺MSC组、OP9组、单纯照射组,正常组明显好于各组(均为P<0.01),单纯照射组明显差于DA组、胚肺MSC组(均为P<0.01);DA组、胚肺MSC组及OP9组的两两配对t检验均为P>0.05。肺病理镜检肺损伤评分均值由高到低顺序为正常组、胚肺MSC组、OP9组、DA组、单纯照射组。肺病理图像分析肺泡情况由好到差顺序为正常组、胚肺MSC组、DA组、OP9组、单纯照射组。外观评分与病理镜检的相关性检验P=0.040,与图像分析的相关性检验P=0.039。结论:不同来源的MSC均有减轻放射性肺损伤的作用,其作用强度相似。 Objective: To compare the role of mesenchymal stem cells (MSC) derived from mouse embryonic lung, bone marrow and embryonic dorsal aorta(DA) area in the treatment of irradiation induced mouse model of lung injury. Methods: The mice were divided randomly into five groups: normal control group(A), irradiation with- out MSC group(B), embryonic lung MSC treatment group(C), OP9 treatment group(D) and DA MSC treatment group(E). Four, nine, thirteen, seventeen and twenty-three weeks after MSC engraftment, the change in appear- ance of the mice in each group was observed, and then their lungs were harvested after the mice were sacrificed. The pathology of the lung structure was observed by HE stalling. Results: The mean score of mice appearance was the highest in group A and the lowest in group B. There were no significant difference in the mean appear- ance score between group C, D and E. The mean alveolitis score was related to the mean appearance score, P= 0.040.The image analysis of alveoli area was related to the mean appearance score, P=0.039. Conclusion: The ex- tent of irradiation induced lung injury could be moderated through the treatment of MSC derived from embryonic lung, OP9 and embryonic dorsal aorta area. The treatment of MSC derived from different tissue is similar.
出处 《生物技术通讯》 CAS 2012年第2期171-175,共5页 Letters in Biotechnology
基金 国家自然科学基金(30972974) 国家重点实验室开放课题(RLO200801)
关键词 放射性肺损伤 间充质干细胞 骨髓 胚肺 胚胎背主动脉区 irradiation induced lung injury mesenchymal stem cells mouse embryonic lung OP9 mouse embry-onic dorsal aorta area
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  • 1Watt FM, Hogan BL. Out of Eden: stem cells and their niches. Science 2000;287(5457):1427-1430.
  • 2Griffiths M J, Bonnet D, Janes SM. Stem cells of the alveolar epithelium. Lancet 2005;366(9481):249-260.
  • 3Neuringer IP, Randell SH. Stem cells and repair of lung injuries. Respir Res 2004;5:6.
  • 4Kotton DN, Summer R, Fine A. Lung stem cells: new paradigms. Exp Hematol 2004;32(4):340-343.
  • 5Hong KU, Reynolds SD, Giangreco A, et al. Clara cell secretory protein-expressing cells of the airway neuroepithelial body microenvironmeat include a label-retaining subset and are critical for epithelial renewal after progenitor cell depletion. Am J Respir Cell Mol Biol 2001 ;24(6):671-681.
  • 6Reynolds SD, Giangreco A, Power JH, et al. Neuroepithelial bodies of pulmonary airways serve as a reservoir of progenitor cells capable of epithelial regeneration. Am J Pathol 2000;156(1):269-278.
  • 7Giangreco A, Reynolds SD, Stripp BR. Terminal bronchioles harbor a unique airway stem cell population that localizes to the bronchoal veolar duct j unction. Am J Pathol 2002; 161 (1): 173 - 182.
  • 8Kim CF, Jackson EL, Woolfenden AE, et al. Identification of bronchioalveolar stem cells in normal lung and lung cancer. Cell 2005; 121 (6): 823-835.
  • 9Ling TY, Kuo MD, Li CL, et al. Identification of pulmonary Oct-4+ stem/progenitor cells and demonstration of their susceptibility to SARS coronavirus (SARS-CoV) infection in vitro. Proc Natl Acad Sci U S A 2006;103(25):9530-9535.
  • 10Giangreco A, Shen H, Reynolds SD, et al. Molecular phenotype of airway side population ceils. Am J Physiol Lung Cell Mol Physiol 2004;286(4):L624-L630.

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  • 1Madani I,De Ruyck K,Goeminne H,et al. Predicting risk ofradiation - induced lung injuryf J]. J Thorac Oncol,2007,2(9) :864-874.
  • 2Anscher MS, raurase T, Prescott DM. Changes in plasmaTGF - pi levels during pulmonary radiotherapy as a predic-tor of risk of developing radiation pneumonitis [ J ]. Int Ra-dial Oncol Biol Phys,2006,30(3) :671 -676.
  • 3Chen Y, Hyrien 0, Williams J, et al. Interleukin( IL) - 1Aand IL - 6 : applications to the predictive diagnostic testingof radiation pneumonitis [ J ]. Int Radial Oncol Biol Phys,2005,62(1):260-266.
  • 4Yuan X,Liao Z,Liu Z,et al. Single nucleotide polymorphismat rsl982073 :T869C of the TGFpl gene is associated withthe risk of radiation pneumonitis in patients with non - small—cell lung cancer treated with definitive radiotherapy[ J].Clin Oncol,2009,27(20) :3370-3378.
  • 5Yang M,Zhang L,Bi N,et al. Association of P53 and ATMpolymorphisms with risk of radiation 一 induced pneumonitisin lung cancer patients treated with radiotherapy [ J ]. IntRadiat Oncol Biol Phys,2011,79(5) :1402 — 1407.
  • 6张健,李宝生,周涛,等.NOS2A和NOS3基因单核苷酸多态性在预测放射性肺损伤中的价值[A]. 2012济南国际放射肿瘤学论坛论文汇编,2012,12(1)=11-19.
  • 7Amalinei C, Caruntu ID, Giusca SE,et al. Matrix metallo-proteinases involvement in pathologic conditions [ J ]. RomJ Morphol Embryol,2010,51(2) :215 -228.
  • 8Cai Y,Zhu L,Zhang F, et al. Non - invasive monitoring ofpulmonary fibrosis by targeting matrix metalloproteinase(MMPs) [ J]. Molecular pharmaceutics, 2013 ,21 ( 3 ) : 23-28.
  • 9爱德华.海普林,卡洛斯.佩雷姿,路德.布莱迪,等.放射肿瘤学原理和实践[M].第5版.天津:天津科技翻译公司出版,2012:1218.
  • 10Flanders KC. Smad3 as a mediator of the fibrotic response[J ]. International Journal of Experimental Pathology,2004,85(2) :47 -64.

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