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核素锝[^(99m)Tc]对维甲酸诱导骨髓间充质干细胞的干预研究

Intervention Study of Retinoic Acid Induced Bone Mesenchymal Stem Cell Differentiated into Neuron with Nuclide Technetium[^(99m)Tc]
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摘要 目的研究核素锝[^(99m)Tc]对大鼠骨髓间充质干细胞诱导分化为神经元样细胞的影响。方法采用密度梯度离心法结合贴壁培养法分离、纯化大鼠骨髓间充质干细胞,以30μmol·L^(-1)维甲酸诱导其向神经元样细胞分化,并测定核素锝[^(99m)Tc]干预骨髓间充质干细胞分化后的生物学影响。结果活度为740、1 110 MBq·mL^(-1)锝[^(99m)Tc]干预骨髓间充质干细胞6 h后,细胞存活率分别为(96.03±2.21)%、(94.47±2.12)%,锝[^(99m)Tc]干预的骨髓间充质干细胞在维甲酸诱导下可表达神经元的特异性标记物Nestin和NSE。结论常规剂量下锝[^(99m)Tc]不影响骨髓间充质干细胞的细胞活力和分化。 Objective To study the impact of [^99m Tc]to bone mesenchymal stem cells (MSCs)induced by retinoic acid to differentiate into neuron-like cell. Methods MSCs were isolated and purified by density gradient centrifugation and adherent culture,and then induced into neuron-like cell by 30 μmol·L ^-1 retinoic acid.Biologcial effects of neuron-like cell were determined after [^99m Tc]interfered in the differentiation of MSCs. Results After the interference of 740、1 1 10 MBq·mL ^-1 [^99m Tc]for 6 hours,cell survival rate was(96.03 ±2.21 )% and (94.47 ±2.12 )% respectively,and Nestin and NSE were expressed in the progress of 740 MBq · mL^ -1 [^99m Tc ] interfering in the differentiation of MSCs. Conclusion The cell viability and differentiation of MSCs were not affected by the conventional dose of [99m Tc]in vitro.
作者 李玮
出处 《河南科技大学学报(医学版)》 2016年第2期84-86,共3页 Journal of Henan University of Science & Technology:Medical Science
关键词 ^99MTC 骨髓间充质干细胞 神经前体细胞 神经元 ^99Tc bone mesenchymal stem cell nerve precursor cell neuron
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  • 1HE Xu,LI Yu-lin,WANG Xin-rui,GUO Xin,NIU Yun.Mesenchymal stem cells transduced by PLEGFP-N1 retroviral vector maintain their biological features and differentiation[J].Chinese Medical Journal,2005(20):1728-1734. 被引量:20
  • 2谢英林,王欣.间充质干细胞制备类人工真皮修复全层皮肤缺损的实验研究[J].中国实验诊断学,2006,10(7):748-749. 被引量:1
  • 3叶千春,王淑侠,乔穗宪,唐安戊,何建军.^(99)Tc^m-MIBI甲状腺显像鉴别甲状腺结节良恶性再认识[J].中华核医学杂志,2006,26(4):209-210. 被引量:16
  • 4YAMAZAKI M, NAKAJIMA F, OGASAWARA A, et al. Spatial and temporal distribution of CD44 and osteopontin in fracture callus [J]. J Bone Joint Surg Br, 1999, 81 (3): 508.
  • 5COLTER D C, CLASS R, DIGIROLA MO C M, et al. Rapid expansion of recycling stem cells in culture of plastic- adherent cells form human bone marrow [J].Proc Natl Acad Sci USA, 2000, 97 (7) : 3213.
  • 6QIU Q, DUCHEYNE P, GAO H, et al. Fonntion and differentiation of three- dimensional rat marrow stromal cell culture on microcarriers in a rotating - wall vessel [J]. Tissue Eng, 1998, 4 (1): 19.
  • 7GLOWACKI J, MIZUNO S, GREENBERGER J S.Perfusion enchances functions of bone marrow stromalcells in three- dimensional culture [ J ]. Cell Transplant. 1998, 7 (3): 319.
  • 8MAKINO S, FUKUDA K, MIYOSHI S, et al.Cardiomyocytes can be generated from marrow stromal cells in vitro [J]. J Cli Invest, 1999, 103 (5):697.
  • 9TOMITA S, LI R K, WEISEL R D, et al. Autologous transplantation of bone marrow cells improves damaged heart function [J]. Circulation, 1999, 100(19Suppl) : Ⅱ247.
  • 10WANG J S, SHUM TIM, D, CHEDRAWY E, et al. The coronary delivery of marrow stromal cells for myocardial regeneration: Pathophysiologic and therapentic implications [J ]. J Thorac Cardiovasc Surg,2001, 122 (4): 699.

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