磁共振成像
磁共振成像
자공진성상
CHINESE JOURNAL OF MAGNETIC RESONANCE IMAGING
2014年
2期
138-143
,共6页
赵江民%刘佳%林雁冰%宗根林%吴利忠%钱海珊%游建雄
趙江民%劉佳%林雁冰%宗根林%吳利忠%錢海珊%遊建雄
조강민%류가%림안빙%종근림%오리충%전해산%유건웅
超顺磁性氧化铁%间质干细胞%生物学标记%磁共振成像
超順磁性氧化鐵%間質榦細胞%生物學標記%磁共振成像
초순자성양화철%간질간세포%생물학표기%자공진성상
Superparamagnetic iron oxides%Mesenchymal stem cells%Biological markers%Magnetic resonance image
目的:观察不同浓度超顺磁性氧化铁(SPIO)标记对干细胞生物学特性的影响及SPIO标记后BMSCs体外的MRI特征。材料与方法分离、培养SD大鼠的BMSCs,取第四代的BMSCs,通过流式细胞仪检测表面抗原。不同浓度的SPIO标记液标记BMSCs,通过普鲁士兰染色检测标记效率,台盼兰活细胞计数检测细胞活力,MTT法检测细胞增殖活性。通过MRI检查,观察体外不同浓度SPIO标记细胞的信号变化情况。结果 SPIO在25~50μg/ml的浓度范围可以安全、高效地标记BMSCs,不会影响BMSCs的表型、活力和增殖等生物学特性;当SPIO浓度在75μg/ml以上时,BMSCs活性及增殖能力逐渐降低。随着SPIO标记浓度的增加,细胞内摄入的铁逐渐增多,而T2信号强度则逐渐降低;当SPIO浓度≥50μg/ml,标记细胞的T2信号强度与普通BMSCs相比较均有明显差异(P<0.05)。结论适当浓度的SPIO标记BMSCs对其生物学活性没有明显影响,且MRI扫描能够有效检测其信号变化。
目的:觀察不同濃度超順磁性氧化鐵(SPIO)標記對榦細胞生物學特性的影響及SPIO標記後BMSCs體外的MRI特徵。材料與方法分離、培養SD大鼠的BMSCs,取第四代的BMSCs,通過流式細胞儀檢測錶麵抗原。不同濃度的SPIO標記液標記BMSCs,通過普魯士蘭染色檢測標記效率,檯盼蘭活細胞計數檢測細胞活力,MTT法檢測細胞增殖活性。通過MRI檢查,觀察體外不同濃度SPIO標記細胞的信號變化情況。結果 SPIO在25~50μg/ml的濃度範圍可以安全、高效地標記BMSCs,不會影響BMSCs的錶型、活力和增殖等生物學特性;噹SPIO濃度在75μg/ml以上時,BMSCs活性及增殖能力逐漸降低。隨著SPIO標記濃度的增加,細胞內攝入的鐵逐漸增多,而T2信號彊度則逐漸降低;噹SPIO濃度≥50μg/ml,標記細胞的T2信號彊度與普通BMSCs相比較均有明顯差異(P<0.05)。結論適噹濃度的SPIO標記BMSCs對其生物學活性沒有明顯影響,且MRI掃描能夠有效檢測其信號變化。
목적:관찰불동농도초순자성양화철(SPIO)표기대간세포생물학특성적영향급SPIO표기후BMSCs체외적MRI특정。재료여방법분리、배양SD대서적BMSCs,취제사대적BMSCs,통과류식세포의검측표면항원。불동농도적SPIO표기액표기BMSCs,통과보로사란염색검측표기효솔,태반란활세포계수검측세포활력,MTT법검측세포증식활성。통과MRI검사,관찰체외불동농도SPIO표기세포적신호변화정황。결과 SPIO재25~50μg/ml적농도범위가이안전、고효지표기BMSCs,불회영향BMSCs적표형、활력화증식등생물학특성;당SPIO농도재75μg/ml이상시,BMSCs활성급증식능력축점강저。수착SPIO표기농도적증가,세포내섭입적철축점증다,이T2신호강도칙축점강저;당SPIO농도≥50μg/ml,표기세포적T2신호강도여보통BMSCs상비교균유명현차이(P<0.05)。결론괄당농도적SPIO표기BMSCs대기생물학활성몰유명현영향,차MRI소묘능구유효검측기신호변화。
Objective:To observe the biological characteristics of rat bone marrow mesenchymal stem cells (BMSCs) labeled by superparamagnetic iron oxide (SPIO) in vitro, and to observe the magnetic resonance imaging (MRI) features of labeled BMSCs in vitro. Materials and Methods: BMSCs were isolated and cultured by plastic adherence method. The BMSCs of the fourth passage were identiifed by speciifc surface antigens by flow cytometr. BMSCs were labeled with SPIO of different concentrations. Trypan blue staining and MTT test to evaluate the effects of SPIO on cell labeling efficiency, cell viability and cell proliferation. The MRI imaging features of labeled BMSCs were observed by MRI scanning. Results:The labeling efifciency of all SPIO groups was about 99%. BMSCs labeled with SPIO-PLL at the concentrations (25, 50 μg/ml SPIO, and 0.75 μg/ml PLL), Cell viability rates were about 95%. While at the concentration of SPIO (75, 100μg/ml), cell viability rate was 92.7%and cell proliferation was significantly inhibited (P<0.05). On MRI imaging, with the concentration of SPIO increasing, signal intensity decreased gradually. When SPIO concentration ≥50 μg/ml, T2 signal intensity of labeled cells compared with normal BMSCs were significantly different (P<0.05). Conclusions:The appropriate concentration of SPIO could not influence on cells biological characteristics. MRI scanning can show the SPIO nanoparticles labeled rat BMSCs significantly and effectively.