期刊文献+

MRI体外定量测定SPIO标记兔骨髓间充质干细胞 被引量:2

MRI Quantitatively Measurement of SPIO-Labeled Mesenchymal Stem Cells in Experimental Rabbits in Vitro
原文传递
导出
摘要 目的测定MRI监测SPIO标记兔骨髓间充质干细胞(r-MSC)的最低SPIO浓度,寻找MRI体外定量测定SPIO标记r-MSC的方法。方法分离、培养r-MSC,不同浓度SPIO标记r-MSC 24 h后采用3.0 T MRI T2*WGRE、T1W-GRE、T2W-PROPELLER序列扫描标本。结果 3种序列中,T2*W-GRE序列体外监测SPIO标记干细胞的能力最佳,1×105/ml、1×106/ml细胞浓度下,T2*W-GRE序列测定的平均MR信号衰减率(△SI)与SPIO浓度之间具有强相关。结论适宜细胞浓度下,T2*W-GRE序列可用于定量近似预测SPIO标记浓度。 Objective To determine the lowest SPIO concentration necessary for MRI monitoring of SPIO-labeled mesenchymal stem cells (r-MSC) in experimental rabbits, and to find out the method for MRI quantitative measurement of r- MSC in vitro. Methods The r-MSC were purified by adherent culture and amplified in vitro. The r-MSC labeled with different concentrations of SPIO was incubated for 24 hour. 3.0 T MR scanning by using T2 * W-GRE, T1W-GRE and T2W-PROPELLER sequences were used to scan these specimens. Results Among the three sequences, T2 * W-GRE sequence was the best sequence in monitoring the SPIO labeled r-MSC. In the situation of cell concentration of 1×10^5/ml and 1 ×10^6/ml, the average MR signal attenuation rate (ASI) hail a close correlation with SPIO concentration. Conclusion In the situation of appropriate cell concentration, i.e. cell concentration of 1×10^5/ml and 1 x 106/ml, T2 * W-GRE sequence can be used to quantitatively measure the approximately SPIO eoncentration.
出处 《临床放射学杂志》 CSCD 北大核心 2015年第4期647-651,共5页 Journal of Clinical Radiology
关键词 兔骨髓间充质干细胞 磁共振成像 超顺磁性氧化铁粒子 T2*W-GRE序列 Rabbit bone marrow mesenehyma| stem cells Magnetic resonance imaging Superparmagnetic iron oxide particles T2 * W-GRE sequence
  • 相关文献

参考文献19

  • 1Sandu N, Schaller B. Molecular imaging of stem cell therapy in brain tumors: a step towards personalized medicine [ J ]. Arch Med Sci, 2012,8:601-605.
  • 2Song F, Tian M, Zhang H. Molecular imaging in stem cell therapy for spinal cord injury[ J]. Biomed Res Int, 2014,2014:759514.
  • 3Kinoshita M, Yoshioka Y, Okita Y, et al. MR molecular imaging of HER-2 in a murine tumor xenograft by SPIO labeling of anti-HER-2 affibody [ J ]. Contrast Media Mol Imaging,2010,5 : 18-22.
  • 4Addicott B, Willman M, Rodriguez J, et al. Mesenchymal stem cell labeling and in vitro MR characterization at 1.5 T of new SPIO con- trast agent: Molday ION Rhodamine-B [ J ]. Contrast Media Mol Ima- ging,2011,6:7-18.
  • 5Rosenberg JT, Sachi-Kocher A, Davidson MW, et al. Intracellular SPIO labeling of microglia: high field considerations and limitations for MR microscopy [ J ]. Contrast Media Mol Imaging, 2012,7 : 121 - 129. .
  • 6Shichinohe H, Kuroda S, Kudo K, et al. Visualization of the Super- paramagnetic Iron Oxide (SPIO)-Labeled Bone Marrow Stromal Cells Using a 3.0-T MRI-a Pilot Study for Clinical Testing of Neuro- transplantation[ J]. Transl Stroke Res, 2012,3:99-106.
  • 7Ramaswamy S, Sehornack PA, Smelko AG, et al. Superparamagnetie iron oxide (SPIO) labeling efficiency and subsequent MRI tracking of native cell populations pertinent to pulmonary heart valve tissue engineering studies[ J]. NMR Biomed,2012,25:410-417.
  • 8Yi T, Lee HJ, Cho YK, et al. Molecular Characterization of Neurally Differentiated Human Bone Marrow-derived Clonal MescnchymalStem Cells[ J ]. Immune Netw ,2014,14:54-65.
  • 9Barberini D J, Freitas NP, Magnon MSi, et al. Equine mesenchymal stem cells from bone marrow, adipose tissue and umbilical cord: im- munophenotypic characterization and differentiation potential [ J ]. Stem Cell Res Ther, 2014,5:25.
  • 10刘康,白亦光,陈竹,韩小伟,杨泽龙,赵明,宋桂芹,冯刚.兔骨髓间充质干细胞的分离培养及鉴定[J].川北医学院学报,2013,28(2):103-106. 被引量:12

二级参考文献25

  • 1师长宏,王晓武,王文勇,施新猷,朱德生,李六金.人肝癌原位移植转移模型特性实验研究[J].中国实验动物学报,2001,9(1):55-61. 被引量:7
  • 2Reynolds BA, Weiss S. Generation of neurons and astrocytes from isolated cells of the adult mammalian central nervous system [ J].Science, 1992, 255(5052) :1707 - 1710
  • 3Davis AA, Temple S. A self-renewing muhipotential stem cells in embryonic rat cerebral cortex[ J]. Nature, 1994,372 ( 6503 ) : 263- 266
  • 4Doetsch F, Garcia-Verdugo JM, Alvarez-Buylla A. Cellular composition and three-dimensional organization of the subventricular germinal zone in the adult mammalian brain [J]. J Neurosci,1997,17 (3) :5046 - 5061
  • 5Gottlieb DI. Large-scale sources of neural stem cells[J]. Annu Bey Neurosci, 2002,25:381 -407
  • 6Lendahl U, Zimmerman LB, Mckay RD. CNS stem cells express a new class of intermediate filament protein [ J ]. Cell, 1990,60 (4) :585 - 595
  • 7Zulewski H, Abraham EJ, Gerlach MJ, et al. Muhipotential nestin-positive stem ceils isolated from adult pancreatic islets differentiate ex vivo into pancreatic endocrine, exocrine, and hepatic phenotypes[ J]. Diabetes ,2001,50 ( 3 ) :521 - 533
  • 8Vescovi AL, Parati EA, Gritti A, et al. Isolation and cloning of multipotentlal stem cells from the embryonic human CNS and establishment of transplantable human neural stem cell lines by epigenetic stlmulation[J]. Exp Neurol,1999,156( 1 ) :71 -83
  • 9Boo L,Selvaratnam L,Tai CC, et al. Expansion and preservation of muhipotentiality of rabbit bone-marrow derived mesenchymal stem cells in dextran -based microcarrier spin culture [ J]. J Mater Sci Mater Med,2011,22(5) :1343 - 1356.
  • 10Seong JM,Kim BC,Park JH,et al. Stem cells in bone tissue engi- neering [ J ]. Biomed Mater, 2010,5 ( 6 ) : 11 - 33.

共引文献14

同被引文献3

引证文献2

二级引证文献1

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部