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不同来源骨髓间充质干细胞对CD34+细胞增殖的影响**
引用本文:王 荣,刘瑞风,张永翠,潘智慧,李 欣,刘小民,尹国华,张 静,张开明. 不同来源骨髓间充质干细胞对CD34+细胞增殖的影响**[J]. 中国组织工程研究, 2012, 16(6): 973-976. DOI: 10.3969/j.issn.1673-8225.2012.06.005
作者姓名:王 荣  刘瑞风  张永翠  潘智慧  李 欣  刘小民  尹国华  张 静  张开明
作者单位:1山西医科大学第二临床医学院,山西省太原市 030001;太原市中心医院,2皮肤科,4心内科,山西省太原市  030009;3中北大学医院大内科,山西省太原市030051
基金项目:国家自然科学基金(30972657),项目名称:银屑病患者骨髓造血干细胞定向分化为T细胞过程Notch信号转导通路的动态研究;山西省自然科学基金(2008011082-2),项目名称:系统性红斑狼疮患者骨髓CD34+细胞体外定向分化的T细胞活性研究。
摘    要:背景:作者前期研究显示,银屑病患者与正常人骨髓间充质干细胞的生物学特性、免疫学反应及抗原提呈功能有明显差异,而与流产胎儿骨髓间充质干细胞无明显差异。目的:观察不同来源骨髓间充质干细胞对正常人骨髓CD34+细胞增殖的影响。方法:密度梯度离心法分离银屑病患者和流产胎儿骨髓单一核细胞并培养、传代,传至第2代72 h后收集培养上清液,流式细胞仪鉴定骨髓CD34+细胞及骨髓间充质干细胞纯度。倒置显微镜下观察培养细胞的生长状态,细胞磁珠分选仪分选出的正常人骨髓CD34+细胞加入骨髓间充质干细胞培养上清液培养24 h 后,四甲基偶氮唑盐比色法检测骨髓CD34+细胞的增殖活性。结果与结论:CD34+细胞加入银屑病患者和流产胎儿骨髓间充质干细胞培养上清培养24 h后,细胞形态无差别。银屑病患者和流产胎儿骨髓间充质干细胞培养上清液对正常人骨髓CD34+细胞增殖的影响差异无显著性意义(P > 0.05)。

关 键 词:银屑病  CD34+细胞  骨髓间充质干细胞  增殖活性  
收稿时间:2011-07-16

Effect of different sources of bone mesenchymal stem cells on CD34+ cell proliferation
Wang Rong,Liu Rui-feng,Zhang Yong-cui,Pan Zhi-hui,Li Xin,Liu Xiao-min,Yin Guo-hua,Zhang Jing,Zhang Kai-ming. Effect of different sources of bone mesenchymal stem cells on CD34+ cell proliferation[J]. Chinese Journal of Tissue Engineering Research, 2012, 16(6): 973-976. DOI: 10.3969/j.issn.1673-8225.2012.06.005
Authors:Wang Rong  Liu Rui-feng  Zhang Yong-cui  Pan Zhi-hui  Li Xin  Liu Xiao-min  Yin Guo-hua  Zhang Jing  Zhang Kai-ming
Affiliation:1Second Clinical Medical College of Shanxi Medical University, Taiyuan  030001, Shanxi Province, China; 2Department of Dermatology, Taiyuan Central Hospital, Taiyuan  030009, Shanxi Province, China; 3Department of Inter Medicine, Hospital of Zhongbei University, Taiyuan 030051, Shanxi Province, China; 4Department of Cardiology, Taiyuan Central Hospital, Taiyuan  030009, Shanxi Province, China
Abstract:BACKGROUND: There are some significant differences of biological characteristics, immunological reaction and antigen presentation between bone mesenchymal stem cells (BMSCs) from psoriasis vulgaris (PV) patients and normal health. But there are no more differences between PV patients and aborted fetus. OBJECTIVE: To study the effect of different sources of BMSCs on CD34+ cell proliferation. METHODS: Mononuclear cells were separated from bone marrow in PV patients and aborted fetus by density gradient centrifugation method, then the cells were cultivated and generated. The cultured supernatant was collected until 72 hours later by spreading to the second generation. The purity of CD34+ cells and BMSCs was detected by flow cytometry. Cells growth was observed under inverted microscope. CD34+ cells from normal human bone marrow were selected by magnetic cell sorting method, and then the cells were cultured in the BMSCs culture supernatant for 24 hours. MTT was used to detect the proliferative activity of CD34+ cells.RESULTS AND CONCLUSION: There was no statistic difference on the morphology of CD34+ cells after cultured in the BMSCs culture supernatant derived from PV patients and aborted fetus for 24 hours. There is no significantly effect of BMSCs culture supernatant derived from PV patients and aborted fetus on the proliferation of CD34+ cells (P > 0.05). 
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