Ejtehadifar Mostafa, Shamsasenjan Karim, Akbarzadehlaleh Parvin, Zahedi Sarah, Kazemi Narjes
Hematology and Oncology Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.
Department of Pharmaceutical Biotechnology, Faculty of Pharmacy, Tabriz University of Medical Sciences, Tabriz, Iran.
Adv Pharm Bull. 2016 Dec;6(4):645-650. doi: 10.15171/apb.2016.079. Epub 2016 Dec 22.
Mesenchymal Stem Cells (MSCs) are the most important members of Bone Marrow (BM) milieu. MSCs affect different kinds of cells, particularly malignant cells of hematologic malignancies, but the effects of MSCs are unclear exactly. Here we analyzed the effects of derived Umbilical Cord Blood-MSCs on proliferation, cell death and some surface markers of U937 cell line in a Co-culture system with MSCs. Here we designed Co-culture systems as a model of BM milieu. We cultured U937 cells on UCB-MSCs and MSCs Conditioned Medium (C.M) driven and then treated U937 cells with optimum concentration of chloride cobalt (CoCl) as a hypoxia-mimetic agent. In addition, we applied suitable concentrations of HO to induce cell death. Proliferation rate, cell death rate and some surface markers of hypoxic U937 cells were analyzed by MTT assay, flow cytometry and Real Time-PCR were flown respectively. UCB-MSCs showed supportive effects on U937 proliferation rate in normoxia and hypoxia. Lethal effect of HO suppressed in the presence of UCB-MSCs in hypoxia and normoxia. Among CD11a, CD14, CD49d, CD54 and CD116 markers, CD49d was down regulated in presence of UCB-MSCs and CD116 was up regulated in hypoxia. Other markers didn't show any significant changes. This work provides evidences that MSCs play critical roles in U937 cells biology. These observations shed new light on MSCs roles and demonstrated that MSCs should be regarded as an important member of BM milieu in several clinical applications such as BM transplantation prognosis and treatment of hematologic malignancies.
间充质干细胞(MSCs)是骨髓微环境中最重要的成员。MSCs会影响不同类型的细胞,尤其是血液系统恶性肿瘤的恶性细胞,但其确切作用尚不清楚。在此,我们在与MSCs的共培养系统中分析了脐带血来源的MSCs对U937细胞系增殖、细胞死亡及一些表面标志物的影响。在此,我们设计了共培养系统作为骨髓微环境的模型。我们将U937细胞培养在脐带血间充质干细胞和间充质干细胞条件培养基(C.M)上,然后用最佳浓度的氯化钴(CoCl)作为缺氧模拟剂处理U937细胞。此外,我们应用合适浓度的HO诱导细胞死亡。分别通过MTT法、流式细胞术和实时定量PCR分析缺氧U937细胞的增殖率、细胞死亡率和一些表面标志物。脐带血间充质干细胞在常氧和缺氧条件下对U937细胞的增殖率具有支持作用。在常氧和缺氧条件下,HO的致死作用在脐带血间充质干细胞存在时受到抑制。在CD11a、CD14、CD49d、CD54和CD116标志物中,CD49d在脐带血间充质干细胞存在时下调,CD116在缺氧时上调。其他标志物未显示任何显著变化。这项工作提供了证据表明间充质干细胞在U937细胞生物学中发挥关键作用。这些观察结果为间充质干细胞的作用提供了新的见解,并表明在诸如骨髓移植预后和血液系统恶性肿瘤治疗等多种临床应用中,间充质干细胞应被视为骨髓微环境的重要成员。