The Third Military Medical University, Department of Hematology, Xinqiao Hospital, Chongqing, China.
Int J Radiat Biol. 2010 Mar;86(3):230-7. doi: 10.3109/09553000903422555.
PURPOSE: There is mounting evidence demonstrating that stromal cell derived factor-1 (SDF-1) plays an important role in homing of hematopoietic progenitor cells to bone marrow. This study was aimed to assess whether bone marrow mesenchymal stem cells overexpressing exogenous SDF-1 could synergistically promote the homing of CD34(+) (Cluster of Differentiation [CD]) cells to bone marrow of lethally irradiated severe combined immunodeficiency (SCID) mice. METHODS: Human SDF-1 complementary Deoxyribonucleic acid (cDNA) was transfected into bone marrow-derived mesenchymal stem cells with recombinant lentiviral vector. The expression of SDF-1 was detected by real-time Polymerase Chain Reaction (PCR) and Enzyme-Linked Immunosorbent Assay (ELISA), and the ex vivo chemotaxis function on CD34(+) cells was measured by coculture system and Transwell system. SDF-1 gene-modified mesenchymal stem cell (MSC) and CD34(+) cells were infused into lethally irradiated SCID mice and the hematopoietic reconstitution in the recipient mice was examined. RESULTS: Messenger ribonucleic acid (mRNA) and protein of SDF-1 in infected MSC were significantly higher than that of the non-infected control MSC (p < 0.05). The infected MSC have significant chemotaxis effect on CD34(+) cells in vitro and promote hematopoietic reconstitution after CD34(+) cell transplantation in vivo. CONCLUSION: MSC with high-level expression of SDF-1 can synergistically promote hematopoietic reconstitution after CD34(+) cell transplantation in lethally irradiated SCID mice.
目的:越来越多的证据表明基质细胞衍生因子-1(SDF-1)在造血祖细胞归巢到骨髓中起着重要作用。本研究旨在评估过表达外源性 SDF-1 的骨髓间充质干细胞是否能协同促进 CD34+(分化群[CD])细胞归巢到致死性辐射严重联合免疫缺陷(SCID)小鼠的骨髓。
方法:用人 SDF-1 互补脱氧核糖核酸(cDNA)转染到重组慢病毒载体的骨髓来源的间充质干细胞。通过实时聚合酶链反应(PCR)和酶联免疫吸附试验(ELISA)检测 SDF-1 的表达,并通过共培养系统和 Transwell 系统检测对 CD34+细胞的体外趋化功能。将 SDF-1 基因修饰的间充质干细胞(MSC)和 CD34+细胞注入致死性辐射的 SCID 小鼠中,检测受体小鼠的造血重建情况。
结果:感染 MSC 的信使核糖核酸(mRNA)和 SDF-1 蛋白明显高于未感染对照 MSC(p<0.05)。感染的 MSC 对 CD34+细胞具有明显的体外趋化作用,并在体内 CD34+细胞移植后促进造血重建。
结论:高表达 SDF-1 的 MSC 可协同促进致死性辐射 SCID 小鼠 CD34+细胞移植后的造血重建。
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