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作 者:李书坛 黄纯兰 LI Shutan;HUANG Chunlan(Department of Hematology, the Affiliated Hospital of Southwestern Medical University, Sichuan Province, Luzhou 646000, Chin)
出 处:《中国医药导报》2018年第12期4-7,24,181,共6页China Medical Herald
基 金:国家自然基金资助项目(81450030);四川省教育厅重大培育项目(14CZ0017)
摘 要:目的研究BMP-2联合人骨髓间充质干细胞(MSC)造血干细胞(HSC)体外增殖的影响。方法培养MSC至第三代,磁珠分选仪分选HSC,并用流式细胞术鉴定MSC与HSC。将获得的MSC与HSC利用Transwell非接触共培养,100 ng/mL的骨形态发生蛋白(BMP-2)干预,即实验分四组:HSC组、HSC+BMP2组、HSC+MSC组、HSC+MSC+BMP2组。培养3 d后比较不同培养条件下HSC计数、RNA浓度的不同,并通过实时荧光定量PCR法及免疫荧光方法检测HSC的Ki67的mRNA及蛋白的表达。结果 HSC的计数、总RNA含量、Ki67的表达在HSC+BMP2组高于HSC组、HSC+MSC组高于HSC组、HSC+MSC+BMP2组高于HSC+MSC组(P<0.05)。结论 MSC协同BMP-2蛋白可促进HSC的增殖。Objective To explore the proliferation effect of bone morphogenetic protein(BMP)-2 on hematopoietic stem cell(HSC) cocultured with mesenchymal stem cell(MSC). Methods MSCs were expanded to the third passage(P3) in the plastic dish; CD34-+cells were sorted by MACS Miltenyi Biotec. MSCs(P3) and HSCs were identified by FCM separately, and then MSC(P3) and HSC were co-cultured in the Transwell interfered with BMP-2 protein, four groups in the study: HSC group, HSC+BMP2 group, HSC+MSC group, HSC+MSC+BMP2 group. Cells were collected after 3 d to test HSC proliferation using the following methods:counting of the number, detecting of the total RNA, the m RNA and protein expression of Ki67 were detected by fluorescence q RT-PCR and immunofluorescence methods. Results The number of HSC, totel RNA, Ki67 expression of the HSC +BMP2 group was higher than HSC group, HSC +MSC group was higher than HSC group, HSC+MSC+BMP2 group was higher than HSC+MSC group(P 〈 0.05). Conclusion MSCs synergistic with BMP-2 can enhance MSC proliferation effect on HSC.
分 类 号:R331.2[医药卫生—人体生理学]
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