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间充质干细胞作为饲养层可防止脐血来源的扩增造血干细胞发生凋亡。

Mesenchymal stem cells as a feeder layer can prevent apoptosis of expanded hematopoietic stem cells derived from cord blood.

作者信息

Mehrasa Roya, Vaziri Hamidreza, Oodi Arezoo, Khorshidfar Mona, Nikogoftar Mahin, Golpour Monireh, Amirizadeh Naser

机构信息

University of Guilan, Rasht, Iran.

Blood Transfusion Research center, High institute for Research and Education in Transfusion Medicine,Tehran, Iran.

出版信息

Int J Mol Cell Med. 2014 Winter;3(1):1-10.

Abstract

Umbilical cord blood (UCB) has been used for transplantation in the treatment of hematologic disorders as a source of hematopoietic stem cells (HSCs). Because of insufficient number of cord blood CD34(+) cells, the expansion of these cells seems to be important for clinical application. Mesenchymal stromal cells (MSCs), playing an important role in HSCs maintenance, were used as feeder layer. Apoptosis and cell cycle distribution of expanded cells were analyzed in MSCs co-culture and cytokine conditions and results were compared. Three culture conditions of cord blood HSCs were prepared ex-vivo for 14 days: cytokines (SCF, TPO and Flt3L) with MSCs feeder layer, cytokines without MSCs feeder layer and co-culture with MSCs without cytokines. Expansion was followed by measuring the total nucleated cells (TNCs), CD34(+) (‏) cells and colony-forming unit (CFU) output. Flow cytometry analysis of stained cells by annexin V and propidium iodide was performed for detection of apoptosis rate and cell cycle distribution in expanded cells. Maximum cord blood CD34(+) cells expansion was observed in day 10. The mean fold change of TNCs and CD34+ cells at day 10 in the co-culture system with cytokines was significantly higher than the cytokine culture without MSCs feeder layer and co-culture system without cytokines (n=6, p=0.023). The highest apoptosis rate and the least number of cells in Go/G1 phase were observed in cytokine culture without feeder layer (p=0.041). The expansion of cord blood HSCs on MSCs as a feeder layer resulted in higher proliferation and reduction in apoptosis rate.

摘要

脐带血(UCB)已作为造血干细胞(HSCs)的来源用于血液系统疾病的移植治疗。由于脐带血CD34(+)细胞数量不足,这些细胞的扩增对于临床应用似乎很重要。在HSCs维持中起重要作用的间充质基质细胞(MSCs)被用作饲养层。分析了在MSCs共培养和细胞因子条件下扩增细胞的凋亡和细胞周期分布,并比较了结果。在体外制备脐带血HSCs的三种培养条件,持续14天:含有MSCs饲养层的细胞因子(SCF、TPO和Flt3L)、不含MSCs饲养层的细胞因子以及不含细胞因子的与MSCs共培养。通过测量总核细胞(TNCs)、CD34(+)(‏)细胞和集落形成单位(CFU)产量来跟踪扩增情况。对用膜联蛋白V和碘化丙啶染色的细胞进行流式细胞术分析,以检测扩增细胞中的凋亡率和细胞周期分布。在第10天观察到脐带血CD34(+)细胞的最大扩增。在含有细胞因子的共培养系统中,第10天TNCs和CD34+细胞的平均变化倍数显著高于不含MSCs饲养层的细胞因子培养和不含细胞因子的共培养系统(n = 6,p = 0.023)。在没有饲养层的细胞因子培养中观察到最高的凋亡率和处于G0/G1期的细胞数量最少(p = 0.041)。以MSCs作为饲养层对脐带血HSCs进行扩增导致更高的增殖和凋亡率降低

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d44/3927388/3265da948d99/ijmcm-3-001-g002.jpg

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