State key laboratory of bioelectronics, School of biological science & medical engineering, Southeast University, Nanjing, 210096, China.
State key laboratory of bioelectronics, School of biological science & medical engineering, Southeast University, Nanjing, 210096, China.
Gene. 2019 May 15;696:10-20. doi: 10.1016/j.gene.2019.02.017. Epub 2019 Feb 12.
Human umbilical cord (UC) and cord blood (CB) provide attractive sources of mesenchymal stem cells (MSCs) for cell therapy. Both UCMSCs and CBMSCs have been demonstrated to play prominent roles in clinical therapy. However, little is known about their functional differences in clinical application. Our transcriptome analysis uncovered high activity of insulin secretion related signaling pathways for CBMSCs and cell adhesion related signaling pathways for UCMSCs. Expression of a large number of immune related signaling pathways also showed the difference in both cells, implying their distinct immune modulatory functions. As the therapeutic effects of MSCs mainly dependent on the cytokines and growth factors produced by transplanted MSCs, we further compared the cytokine profiles of UCMSCs and CBMSCs using antibody array. By evaluating the expression of 106 cytokines, we found both MSCs abundantly secreted TSP-1, TSG-14, TIMP-1, IL-8, IL-6, CXCL1, GIF and IGFBP3. However, the expression of CCL2 in UCMSCs showed significantly higher than CBMSCs. IGFBP1 and IGFBP2 were secreted by CBMSCs with higher abundance than UCMSCs. Overall, these results suggest that UCMSCs and CBMSCs preserve different functional potentials, which have to be carefully considered before clinical treatment.
人类脐带(UC)和脐带血(CB)为细胞治疗提供了有吸引力的间充质干细胞(MSCs)来源。UCMSCs 和 CBMSCs 均已被证明在临床治疗中发挥重要作用。然而,对于它们在临床应用中的功能差异知之甚少。我们的转录组分析揭示了 CBMSCs 中胰岛素分泌相关信号通路和 UCMSCs 中细胞黏附相关信号通路的高活性。大量免疫相关信号通路的表达也表明了两种细胞之间的差异,暗示了它们不同的免疫调节功能。由于 MSC 的治疗效果主要取决于移植的 MSC 产生的细胞因子和生长因子,我们使用抗体阵列进一步比较了 UCMSCs 和 CBMSCs 的细胞因子谱。通过评估 106 种细胞因子的表达,我们发现两种 MSC 都大量分泌 TSP-1、TSG-14、TIMP-1、IL-8、IL-6、CXCL1、GIF 和 IGFBP3。然而,UCMSCs 中 CCL2 的表达明显高于 CBMSCs。IGFBP1 和 IGFBP2 由 CBMSCs 分泌,其丰度高于 UCMSCs。总的来说,这些结果表明 UCMSCs 和 CBMSCs 具有不同的功能潜力,在临床治疗前必须仔细考虑。