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硫酸酯酶2型基因体内表达促进5-氟脲嘧啶诱发的小鼠骨髓抑制恢复作用研究

Protective Effect of Sulfatase 2 Gene Expression on Mice Myelodepression Induced by 5-Fluorouracil Injection

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【作者】 毛文伟王霞梁迁何慧娟魏兆莲林小娟黄薇薇吴明媛朱顺英路慧丽王群韩伟

【Author】 MAO Wen-wei1 WANG Xia1 LIANG Qian1 HE Hui-juan1 WEI Zhao-lian2 LIN Xiao-juan1 HUANG Wei-wei1 WU Ming-yuan1 ZHU Shun-ying1 LU Hui-li1 WANG Qun1 HAN Wei1(1 Lab of Regenerative Medicine, School of Pharmacy, Shanghai Jiaotong University, Shanghai 200240,China)(2 Department of Obstetrics and Gynecology,the First Affiliated Hospital, Anhui Medical University,Hefei 230022, China)

【机构】 上海交通大学药学院再生医药学实验室安徽医科大学第一附属医院妇产科

【摘要】 采用半定量RT-PCR和重组基因体内表达法观察了硫酸酯酶2基因(Sulfatase 2,Sulf2)在5-氟脲嘧啶(5-Fluorouracil,5-Fu)诱发的小鼠骨髓抑制和再生过程中作用。结果表明:Sulf2在小鼠骨髓抑制和再生过程中呈现先上升,后下降的动态表达;电转pcDNA3.1-Sulf2基因实验组外周血白细胞数和血小板数在5-Fu注射后第7天分别为(1216.7±457.9)/μl和(8.1±5.4)万/μl,明显低于对照组[分别为(1691.7±228.9)/μl和(14.7±2.1)万/μl],实验组单条腿骨髓细胞总数在第7天为(94.2±21.1)万,显著低于对照组(173±59.9)万,但在第11天为(585±337.9)万,又显著地高于对照组(255±65.3)万,实验组第7天10000个骨髓细胞总集落形成数为(9±8.4),显著低于对照组(39±12.2),统计均有显著性差异(p<0.05)。这些结果提示Sulf2可能对5-Fu诱发的小鼠骨髓抑制后的再生具有促进作用。

【Abstract】 The aim of the study is to observe the regulation role of sulfatase 2 gene fragment in vivo expression on mouse myelodepression induced by 5-fluorouracil injection. The recombinant pcDNA3.1-Sulf2 eukaryotic expression vector was constructed using gene cloning method,mice bone marrow depression and regeneration model was established by injection of 5-fluorouracil (250mg/kg) via mice tail vein. 50μg of pcDNA3.1-Sulf2 recombinant eukaryotic expression vector (experimental group) was injected into the tibial muscle of each mouse, then introduced into muscle cells for expression by electroporation on the first day after 5-fluorouracil injection, so did the control group which injected and electroporated with the same quantity of pcDNA3.1 blank plasmid . Mice peripheral blood cells and platelets were calculated via automatic blood cells analyzer, and bone marrow cells per leg of each mouse was counted by hemacytometer on day 0 before injection of 5-fluorouracil and on day 3, day 7,day 11,day 14 after injection of 5-fluorouracil respectively. Colony forming test were carried out between the experimental group and control group on day 7 and day 14. The numbers of peripheral blood cells and platelets in experimental group on day 7 were significantly lower than those in the control group respectively [(1216.7±457.9)μl, n=6 versus(1691.7±228.9)μl, n=6; and (8.1±5.4)×104/μl, n=6 versus (14.7±2.1)×104/μl, n=6, respectively, p<0.05].The total bone marrow cells per single leg on day 7 in experimental group were (94.2±21.1)×104 (n=6),and significantly lower than the control group (173±59.9)×104(n=6, p<0.05), but there was a significantly higher numbers of bone marrow cells per leg on day 11 in experimental group (585±337.9)×104(n=6) than in the control group (255±65.3)×104(n=6, p<0.05). Colony forming tests showed that the total colonies per 10000 of bone marrow cells on day 7 of experimental group was at 9±8.4 (n=4), significantly lower than that in control group 39±12.2(n=4, p<0.05), while there was no statistical significance between experimental group (23.3±7.6) per 1000 of bone marrow cells(n=4) and control group (28±6.1) per 1000 of bone marrow cells (n=3, p>0.05) on day 14. The results indicated that there is a protective effect of sulfatase 2 gene expression on the regeneration of mouse bone marrow depressed by 5-fluorouracil.

【基金】 国家“863”计划(2007AA02Z149);国家自然科学基金(30570787,30572214);上海市科学技术委员会生物医药重大科技攻关(05DZ19319)资助项目
  • 【文献出处】 中国生物工程杂志 ,China Biotechnology , 编辑部邮箱 ,2008年11期
  • 【分类号】Q3
  • 【下载频次】148
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