Darvish Maryam, Payandeh Zahra, Soleimanifar Fatemeh, Taheri Behnaz, Soleimani Masoud, Islami Maryam
Department of Medical Biotechnology, Faculty of Medicine, Arak University of Medical Science, Arāk, Iran.
Immunology Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.
J Cell Biochem. 2019 Jul;120(7):12018-12026. doi: 10.1002/jcb.28487. Epub 2019 Feb 25.
Umbilical cord blood (UCB) hematopoietic stem cells (HSCs) transplantation (HSCTs) is considered as a therapeutic strategy for malignant and nonmalignant hematologic disorders. Nevertheless, the low number of HSCs obtained from each unit of UCB can be a major challenge for using these cells in adults. In addition, UCB is a rich source of mesenchymal stem cells (MSCs) creating hopes for nonaggressive and painless treatment in tissue engineering compared with bone marrow MSCs. This study was designed to evaluate the effects of UCB-MSCs application in UCB-HSCs expansion on the nanoscaffold that mimics the cell's natural niche. To achieve this goal, after flow cytometry confirmation of isolated HSCs from UCB, they were expanded on three-dimensional (3D) poly-l-lactic acid (PLLA) scaffolds fabricated by electrospinning and two-dimensional (2D)-culture systems, such as (1) HSCs-MSCs culturing on the scaffold, (2) HSCs culturing on the scaffold, (3) HSCs-MSCs culturing on 2D, and (4) HSCs culturing on 2D. After 7 days, real-time polymerase chain reaction (PCR) was performed to evaluate the CXCR4 gene expression in the mentioned groups. Moreover, for the next validation, the number of total HSCs, 3-(4,5-dimethylthiazol-2-yl)-2,5 diphenyl tetrazolium bromide assay, scanning electron microscopy imaging, and colony-forming unit assay were evaluated as well. The results of the study indicated that UCB-MSCs interaction with HSCs in 3D-culture systems led to the highest expansion of UCB-HSCs on day 7. Flow cytometry results showed the highest purity of HSCs cocultured with MSCs. Real-time PCR showed a significant increase in gene expression of CXCR4 in the mentioned group. The highest viability and clonogenicity were detected in the mentioned group too. Considered together, our results suggest that UCB-HSCs and MSCs coculturing on PLLA scaffold could provide a proper microenvironment that efficiently promotes UCB-HSCs expansion and UCB-MSCs can also be considered as a promising candidate for UCB-HSCTs.
脐带血(UCB)造血干细胞(HSCs)移植(HSCTs)被视为治疗恶性和非恶性血液系统疾病的一种治疗策略。然而,从每个单位的脐带血中获得的造血干细胞数量较少,这可能是在成人中使用这些细胞的一个主要挑战。此外,脐带血是间充质干细胞(MSCs)的丰富来源,与骨髓间充质干细胞相比,为组织工程中的非侵袭性和无痛治疗带来了希望。本研究旨在评估脐带血间充质干细胞在模仿细胞天然微环境的纳米支架上应用于脐带血造血干细胞扩增的效果。为实现这一目标,在通过流式细胞术确认从脐带血中分离出造血干细胞后,将它们在通过静电纺丝制造的三维(3D)聚左旋乳酸(PLLA)支架和二维(2D)培养系统上进行扩增,例如(1)造血干细胞 - 间充质干细胞在支架上共培养,(2)造血干细胞在支架上培养,(3)造血干细胞 - 间充质干细胞在二维培养,以及(4)造血干细胞在二维培养。7天后,进行实时聚合酶链反应(PCR)以评估上述组中CXCR4基因的表达。此外,为了进一步验证,还评估了总造血干细胞数量、3 -(4,5 - 二甲基噻唑 - 2 - 基)- 2,5 - 二苯基溴化四氮唑试验、扫描电子显微镜成像和集落形成单位试验。研究结果表明,在三维培养系统中脐带血间充质干细胞与造血干细胞的相互作用导致第7天脐带血造血干细胞的扩增最高。流式细胞术结果显示与间充质干细胞共培养的造血干细胞纯度最高。实时PCR显示上述组中CXCR4的基因表达显著增加。在上述组中也检测到最高的活力和克隆形成能力。综合考虑,我们的结果表明,在PLLA支架上脐带血造血干细胞和间充质干细胞共培养可以提供一个合适的微环境,有效地促进脐带血造血干细胞的扩增,并且脐带血间充质干细胞也可被视为脐带血造血干细胞移植的一个有前景的候选者。