CAJ | 학술논문

目的探讨脐血源间充质干细胞联合外源性细胞因子对脐血单个核细胞体外扩增的支持作用.方法从脐血中分离、培养出间充质干细胞并检测其细胞表面抗原;以此间充质干细胞作为细胞滋养层.将脐血单个核细胞接种于无血清培养体系中培养18天,在第0、7、10、14及18天检测有核细胞总数、CD34+、CDl33+细胞数、集落形成单位数和(G2+M+S)期细胞含量变化.结果 ①从脐血中分离、培养出的间充质干细胞能稳定表达CD29、CD105和CD44,但不表达CD34和CD133;②外源性细胞因子及脐血源间充质下细胞均支持脐血间充质干细胞扩增,但以细胞因子联合脐血源间充质干细胞组效果最好,在第10天上述榆测指标达到峰值,分别为第0天的(6.91±1.91)、(7.75±1.24)、(6.49±1.33)、(15.62±1.29)和(28.26±6.58)倍,且维持造血至少18天.结论 ①从脐血巾能成功分离、培养出间充质下细胞,并完成细胞表型的初步鉴定;②外源性细胞因子联合脐血源间允质干细胞可有效扩增脐血单个核细胞.
목적 탐토제혈원간충질간세포연합외원성세포인자대제혈단개핵세포체외확증적지지작용.방법 종제혈중분리、배양출간충질간세포병검측기세포표면항원;이차간충질간세포작위세포자양층.장제혈단개핵세포접충우무혈청배양체계중배양18천,재제0、7、10、14급18천검측유핵세포총수、CD34+、CDl33+세포수、집락형성단위수화(G2+M+S)기세포함량변화.결과 ①종제혈중분리、배양출적간충질간세포능은정표체CD29、CD105화CD44,단불표체CD34화CD133;②외원성세포인자급제혈원간충질하세포균지지제혈간충질간세포확증,단이세포인자연합제혈원간충질간세포조효과최호,재제10천상술유측지표체도봉치,분별위제0천적(6.91±1.91)、(7.75±1.24)、(6.49±1.33)、(15.62±1.29)화(28.26±6.58)배,차유지조혈지소18천.결론 ①종제혈건능성공분리、배양출간충질하세포,병완성세포표형적초보감정;②외원성세포인자연합제혈원간윤질간세포가유효확증제혈단개핵세포.
Objective To explore the effects on umbilical cord blood mesenchymal stem cells (UCB-MSCs) combined with exogenous cytokines in supporting the expansion of umbilical cord blood mononuclear cells(UCB MNCs). Methods Mesenchymal stem cells (MSCs) were isolated from umbilical cord blood, and then were detected the cellular surface antigens. The UCB-MNCs were euhured in a serum-free system for 18 days. On day 0, 7, 10, 14 and 18, total mononuclear cells、CD34 cells、CD133 cells、cellular cycle and isolated and cultured from umbilical cord blood were negative for CD34 and CD133, but positive for CD29, The expansion combined with UCB-MSCs and exogenous cytokines had better effect than another groups. The above parameters reached the peak values on day 10. The culture system could maintain at least 18 efficiently support the expansion of UCB-MNCs.