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异基因骨髓移植小鼠联合输注IL-3/IL-6双基因转导的骨髓基质细胞促进造血恢复 被引量:2
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作者 蒋激扬 金永柱 +2 位作者 郝洁 张庆殷 谢蜀生 《中国实验血液学杂志》 CAS CSCD 2002年第5期377-382,共6页
探讨用逆转录病毒载体转入IL 3和IL 6双基因的骨髓基质细胞系QXMSC1IL 3/IL 6对异基因骨髓移植小鼠造血功能的促进作用。用逆转录病毒载体 (含小鼠IL 3cDNA ,人IL 6cDNA)分别转导到骨髓基质细胞系QXMSC1(H 2 d) ,构建骨髓基质细胞系QXMS... 探讨用逆转录病毒载体转入IL 3和IL 6双基因的骨髓基质细胞系QXMSC1IL 3/IL 6对异基因骨髓移植小鼠造血功能的促进作用。用逆转录病毒载体 (含小鼠IL 3cDNA ,人IL 6cDNA)分别转导到骨髓基质细胞系QXMSC1(H 2 d) ,构建骨髓基质细胞系QXMSC1IL 3/IL 6。供体小鼠BALB/c(H 2 d)骨髓去除骨髓中T细胞 ,受体小鼠C57BL/6(H 2 b)经γ射线致死量照射后 ,输入去除T细胞的供体骨髓 (1× 1 0 7/鼠 )的同时输入骨髓基质细胞QXMSC1IL 3/IL 6(5× 1 0 5/鼠 )。在骨髓移植后 2 0和 40天 ,分别检测骨髓移植小鼠外周血RBC ,WBC和骨髓有核细胞数及骨髓中CFU S ,CFU GM ,CFU E和CFU GEMM数。结果 :异基因骨髓移植共输入QXMSC1IL 3/IL 6基质细胞系可使异基因骨髓移植小鼠外周血RBC ,WBC数明显恢复 ,骨髓中有核细胞数 ,CFU S ,CFU GM ,CFU E和CFU GEMM明显增加。基质细胞系QXMSC1可作为有效的基因载体促进骨髓移植后造血功能重建。结论 :基质细胞转入细胞因子IL 3或IL 6基因可以进一步促进骨髓移植后造血功能重建 ,联合转导IL 3和IL 展开更多
关键词 骨髓基质细胞 双基因转导 白细胞介素—3 白细胞介素—6 异基因骨髓移植 造血机能
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人参总皂甙诱导IL-3基因表达的实验研究
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作者 王璐 王亚平 《重庆医科大学学报》 CAS CSCD 2004年第1期31-33,40,共4页
目的 :研究人参总皂甙 (TSPG)对人早期造血生长因子IL - 3基因表达的影响。方法 :采用逆转录聚合酶链反应(RT -PCR)、核酸分子原位杂交方法。结果 :未经诱导的人T淋巴瘤细胞株—Jurkat细胞RNA提取物的RT -PCR扩增产物中未见IL - 3条带 ... 目的 :研究人参总皂甙 (TSPG)对人早期造血生长因子IL - 3基因表达的影响。方法 :采用逆转录聚合酶链反应(RT -PCR)、核酸分子原位杂交方法。结果 :未经诱导的人T淋巴瘤细胞株—Jurkat细胞RNA提取物的RT -PCR扩增产物中未见IL - 3条带 ,而经TSPG诱导后Jurkat细胞RNA提取物的RT -PCR扩增产物中出现IL - 3条带。核酸分子原位杂交显示经TSPG诱导的胎儿胸腺细胞、脾细胞IL - 3mRNA表达的阳性率及阳性强度较对照组均有显著提高。结论 :人参总皂甙能诱导人淋巴细胞表达IL - 3mRNA ,从而促进人早期血细胞发生。 展开更多
关键词 人参总皂甙 造血生长因子 白细胞介素—3 基因表达
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Regulatory effects of moxibustion on ubiquitin and NLRP3 proteins in colon of ulcerative colitis rats 被引量:3
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作者 Li Xi-ying Yang Guang +10 位作者 Wu Li-jie Hong Jue Zhao Yue Liu Jie Kong Xie-he Dong Xiao-qing Zhi Fang-yuan Ma Xiao-peng Yang Ling Zhang Dan Yang Yan-ping 《Journal of Acupuncture and Tuina Science》 CSCD 2020年第2期96-104,共9页
Objective:To observe the effects of moxibustion on colonic inflammation,and the expressions of ubiquitin and nucleotide-binding oligomerization domain(Nod)-Iike receptor protein 3(NLRP3)proteins in rats with ulcerativ... Objective:To observe the effects of moxibustion on colonic inflammation,and the expressions of ubiquitin and nucleotide-binding oligomerization domain(Nod)-Iike receptor protein 3(NLRP3)proteins in rats with ulcerative colitis(UC),and to explore the anti-inflammatory mechanism of moxibustion in the UC treatment.Methods:Clean grade male Sprague-Dawley(SD)rats were randomly divided into a normal group(NG),a model group(MG),a moxa-stick moxibustion group(MSMG)and a Western medicine group(WMG).UC model was prepared by freely drinking 35 g/L d ext ran sulfate sodium(DSS)solution.Bilateral Tianshu(ST 25)were selected for mild moxibustion treatment in the MSMG;mesalazine solution was intragastrically administrated in the WMG.Rats in the NG and MG were only grasped and fixed as in the MSMG without any treatment.After treatment,hematoxylin-eosin(HE)staining was performed to observe and score the colonic pathological damage under light microscope;immunofluorescence method was used to determine the expression of colonic ubiquitin protein;immunohistochemical method was used to detect the expressions of colonic interleukin(IL)-1β and NLRP3 proteins.Results:The colon tissue was severely injured,and the pathological score was significantly increased in the MG than in the NG(P<0.01),and the protein expressions of ubiquitin,NLRP3 and IL-1β in the colon were significantly increased(all P<0.01).Compared with the MG,the colonic damage was repaired,the inflammation and pathological scores were reduced,and the ubiquitin,NLRP3 and IL-1β protein expressions were decreased in the MSMG and WMG(all P<0.01).Correlation analysis revealed that the ubiquitin protein expression was correlated with the colonic pathological score and the NLRP3 protein expression(r=0.677,P<0.01;r=0.536,P<0.05).Conclusion:Moxibustion can down-regulate the protein expressions of ubiquitin,NLRP3 and IL-1β in the colon of UC rats,which may be one of the mechanisms to promote the repair of colonic inflammatory lesions and exert anti-inflammatory effects. 展开更多
关键词 Moxibustion Therapy Moxa Stick Moxibustion Point Tianshu(ST 25) Colitis ULCERATIVE UBIQUITIN NLRP3 Protein Interleukin-lbeta RATS
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