The Second Clinical Medical College, Shanxi Medical University, Taiyuan, China.
Joint Laboratory of Stem Cell Clinical Transformation and Research in Shanxi Province, Taiyuan, China.
J Cell Biochem. 2024 Jan;125(1):79-88. doi: 10.1002/jcb.30505. Epub 2023 Nov 22.
Umbilical cord blood (UCB) is a valuable source of hematopoietic stem cells (HSCs) used for transplantation; the number of cells in a single UCB is too small to quickly establish bone marrow (BM) implantation, and ex vivo expansion of HSCs has the potential to overcome this limitation. The purpose of this study is to explore the culture conditions conducive to the maintenance and expansion of hematopoietic stem and progenitor cells (HSPCs) and long-term hematopoietic stem cells (LT-HSCs) derived from human umbilical cord blood, compare the different effects of albumin (HSA) and polyvinyl alcohol (PVA), optimize the culture system using UM171 and investigate the molecular mechanism of PVA and UM171 promoting the expansion of primitive hematopoietic stem cells. CD34+ cells were purified from UCB using MacsCD34 beads, and then cultured in serum-free medium supplemented with cytokines for 12 days, with PVA or UM171 added according to experimental requirements; the relative percentage of different HSCs subsets after culture were detected by flow cytometry; CFU Assay Setup for detecting the multilineage differentiation potential of HSCs; RT-PCR detection of gene expression levels; reactive oxygen detection assessment of intracellular ROS levels. (1) The conditions of 20 ng/mlSCF, 100 ng/mlTPO, and 5% oxygen concentration are conducive to the maintenance of LT-HSCs. (2) Compared with HSA, PVA significantly increased the proportion of HSPCs and LT-HSCs, as well as dramatically promoted the expression of antioxidant enzymes and reduced the production of reactive oxygen species (ROS). (3) After adding UM171 to PVA-based medium, the proportion of HSPCs and LT-HSCs further increased, and downstream genes of Notch and Wnt pathways were selectively activated. (1) PVA may inhibit ROS production by upregulating the expression of antioxidant enzymes, which is beneficial for maintaining stemness and inhibiting differentiation of HSCs. (2) The antioxidant properties of PVA can delay differentiation, while UM171 can promote self-renewal by regulating the stem cell pathway, and the combination of them is beneficial for the maintenance and expansion of HSCs in vitro.
脐带血(UCB)是一种宝贵的造血干细胞(HSCs)来源,可用于移植;单个 UCB 中的细胞数量太少,无法快速建立骨髓(BM)植入,体外扩增 HSCs 有可能克服这一限制。本研究旨在探索有利于维持和扩增人脐带血来源的造血干/祖细胞(HSPCs)和长期造血干细胞(LT-HSCs)的培养条件,比较白蛋白(HSA)和聚乙烯醇(PVA)的不同作用,优化使用 UM171 的培养系统,并研究 PVA 和 UM171 促进原始造血干细胞扩增的分子机制。使用 MacsCD34 珠从 UCB 中纯化 CD34+细胞,然后在补充细胞因子的无血清培养基中培养 12 天,根据实验要求添加 PVA 或 UM171;通过流式细胞术检测培养后不同 HSCs 亚群的相对百分比;CFU 测定用于检测 HSCs 的多谱系分化潜能;RT-PCR 检测基因表达水平;活性氧检测评估细胞内 ROS 水平。(1)20ng/mlSCF、100ng/mlTPO 和 5%氧浓度的条件有利于维持 LT-HSCs。(2)与 HSA 相比,PVA 显著增加了 HSPCs 和 LT-HSCs 的比例,同时显著促进了抗氧化酶的表达并减少了活性氧物质(ROS)的产生。(3)在添加 UM171 到基于 PVA 的培养基中后,HSPCs 和 LT-HSCs 的比例进一步增加,Notch 和 Wnt 途径的下游基因被选择性激活。(1)PVA 可能通过上调抗氧化酶的表达来抑制 ROS 的产生,这有利于维持 HSCs 的干性并抑制其分化。(2)PVA 的抗氧化特性可以延迟分化,而 UM171 可以通过调节干细胞途径促进自我更新,两者的结合有利于体外维持和扩增 HSCs。