中国比较医学杂志
中國比較醫學雜誌
중국비교의학잡지
CHINESE JOURNAL OF COMPARATIVE MEDICINE
2015年
6期
32-35,83
,共5页
秦力维%张宁坤%路平%彭秀军%王桂琴%高原%曹利群%崔蓓%郭建巍
秦力維%張寧坤%路平%彭秀軍%王桂琴%高原%曹利群%崔蓓%郭建巍
진력유%장저곤%로평%팽수군%왕계금%고원%조리군%최배%곽건외
靶向%脐带间充质干细胞%慢病毒%脾脏
靶嚮%臍帶間充質榦細胞%慢病毒%脾髒
파향%제대간충질간세포%만병독%비장
Targeted umbilical cord derived mesenchymal stem cells%Lentivirus%Spleen%Mice
目的:构建含小分子肽P1-GFP融合基因慢病毒载体,用携带P1-GFP融合基因的慢病毒感染MSC,使MSC具有靶向性,将靶向MSC注入小鼠体内后观察MSC在小鼠脾脏的定位及与淋巴细胞的关系。方法用组织片贴壁法培养健康人脐带间充质干细胞,用基因工程技术构建含小分子肽P1-GFP融合基因慢病毒载体并感染人脐带间充质干细胞,通过尾静脉将转入P1-GFP融合基因的MSC注入小鼠体内,18 h后免疫组化染色观察GFP在小鼠脾脏的定位。结果培养的健康人脐带间充质干细胞生长良好, MSC感染含P1-GFP融合基因的慢病毒18 h后MSC开始出现绿色荧光,随着培养时间的延长,荧光强度逐渐增强,72 h达高峰。靶向MSC表达髓系干细胞的表面标记CD105(90.0%)/CD44(98%),CD73(85.0%)/CD90(98.5%)。将靶向MSC经尾静脉注入小鼠体内,18 h后小鼠脾脏出现大量GFP阳性细胞,并与脾脏淋巴细胞密切接触。结论本研究成功构建了含P1-GFP融合基因的靶向MSC,靶向MSC成功定向脾脏,并与脾脏淋巴细胞密切接触,可用于后续的实验研究。
目的:構建含小分子肽P1-GFP融閤基因慢病毒載體,用攜帶P1-GFP融閤基因的慢病毒感染MSC,使MSC具有靶嚮性,將靶嚮MSC註入小鼠體內後觀察MSC在小鼠脾髒的定位及與淋巴細胞的關繫。方法用組織片貼壁法培養健康人臍帶間充質榦細胞,用基因工程技術構建含小分子肽P1-GFP融閤基因慢病毒載體併感染人臍帶間充質榦細胞,通過尾靜脈將轉入P1-GFP融閤基因的MSC註入小鼠體內,18 h後免疫組化染色觀察GFP在小鼠脾髒的定位。結果培養的健康人臍帶間充質榦細胞生長良好, MSC感染含P1-GFP融閤基因的慢病毒18 h後MSC開始齣現綠色熒光,隨著培養時間的延長,熒光彊度逐漸增彊,72 h達高峰。靶嚮MSC錶達髓繫榦細胞的錶麵標記CD105(90.0%)/CD44(98%),CD73(85.0%)/CD90(98.5%)。將靶嚮MSC經尾靜脈註入小鼠體內,18 h後小鼠脾髒齣現大量GFP暘性細胞,併與脾髒淋巴細胞密切接觸。結論本研究成功構建瞭含P1-GFP融閤基因的靶嚮MSC,靶嚮MSC成功定嚮脾髒,併與脾髒淋巴細胞密切接觸,可用于後續的實驗研究。
목적:구건함소분자태P1-GFP융합기인만병독재체,용휴대P1-GFP융합기인적만병독감염MSC,사MSC구유파향성,장파향MSC주입소서체내후관찰MSC재소서비장적정위급여림파세포적관계。방법용조직편첩벽법배양건강인제대간충질간세포,용기인공정기술구건함소분자태P1-GFP융합기인만병독재체병감염인제대간충질간세포,통과미정맥장전입P1-GFP융합기인적MSC주입소서체내,18 h후면역조화염색관찰GFP재소서비장적정위。결과배양적건강인제대간충질간세포생장량호, MSC감염함P1-GFP융합기인적만병독18 h후MSC개시출현록색형광,수착배양시간적연장,형광강도축점증강,72 h체고봉。파향MSC표체수계간세포적표면표기CD105(90.0%)/CD44(98%),CD73(85.0%)/CD90(98.5%)。장파향MSC경미정맥주입소서체내,18 h후소서비장출현대량GFP양성세포,병여비장림파세포밀절접촉。결론본연구성공구건료함P1-GFP융합기인적파향MSC,파향MSC성공정향비장,병여비장림파세포밀절접촉,가용우후속적실험연구。
Objective To construct lentiviral vectors containing peptide P1-GFP fusion genes.Umbilical cord derived mesenchymal stem cells were infected with lentivirus carrying peptide P1 and GFP fusion genes.To inject the targeted umbilical cord derived mesenchymal stem cells into mice and to detect GFP expression in the spleen.Methods Umbilical cord derived mesenchymal stem cells were cultured with adhered tissues of umbilical cord smaller than 1 mm3 . Lentiviral vector containing P1-GFP fusion genes with engineering technology was constructed and infected the umbilical cord derive mesenchymal stem cells.Targeted umbilical cord derived mesenchymal stem cells were intravenously injected in the mouse tail vein and after 18 hours GFP expression was detected with immunohistochamical staining of the spleen tissues.Results Harvested umbilical cord derived mesenchymal stem cells grew well in culture medium. Green fluorescence on umbilical cord derived mesenchymal stem cells were observed under fluorescence microscope at 18 hours after infected with lentivirus.Green fluorescence intensity of umbilical cord derived mesenchymal stem cells was increasing over time and reached a peak at 72 hours.Umbilical cord derived mesenchymal stem cells highly expressed CD105 (90.0%)/CD44 (98%) and CD73 (85.0%)/CD90 (98.5%) molecules.GFP expression was detected in the spleen after intravenous injection of targeted umbilical cord derived mesenchymal stem cells in the mice 18 hours later.GFP expressing cells intimately contacted with lymphocytes.Conclusions Targeted umbilical cord derived mesenchymal stem cells contain P1-GFP fusion genes are constructed.Targeted umbilical cord derived mesenchymal stem cells can be targeted to mouse spleen and intimately contact with lymphocytes after intravenous injection.Our results lay the groundwork for further studies.