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Conditioned Medium from Human Tonsil-Derived Mesenchymal Stem Cells Enhances Bone Marrow Engraftment via Endothelial Cell Restoration by Pleiotrophin

机译:来自人扁桃体衍生的间充质干细胞的调节培养基通过肺炎素通过内皮细胞恢复增强骨髓植入

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摘要

Cotransplantation of mesenchymal stem cells (MSCs) with hematopoietic stem cells (HSCs) has been widely reported to promote HSC engraftment and enhance marrow stromal regeneration. The present study aimed to define whether MSC conditioned medium could recapitulate the effects of MSC cotransplantation. Mouse bone marrow (BM) was partially ablated by the administration of a busulfan and cyclophosphamide (Bu-Cy)-conditioning regimen in BALB/c recipient mice. BM cells (BMCs) isolated from C57BL/6 mice were transplanted via tail vein with or without tonsil-derived MSC conditioned medium (T-MSC CM). Histological analysis of femurs showed increased BM cellularity when T-MSC CM or recombinant human pleiotrophin (rhPTN), a cytokine readily secreted from T-MSCs with a function in hematopoiesis, was injected with BMCs. Microstructural impairment in mesenteric and BM arteriole endothelial cells (ECs) were observed after treatment with Bu-Cy-conditioning regimen; however, T-MSC CM or rhPTN treatment restored the defects. These effects by T-MSC CM were disrupted in the presence of an anti-PTN antibody, indicating that PTN is a key mediator of EC restoration and enhanced BM engraftment. In conclusion, T-MSC CM administration enhances BM engraftment, in part by restoring vasculature via PTN production. These findings highlight the potential therapeutic relevance of T-MSC CM for increasing HSC transplantation efficacy.
机译:已普遍据报道,利用造血干细胞(HSCs)与造血干细胞(HSC)的COTAspAlantation促进HSC植入并增强骨髓基质再生。本研究旨在定义MSC条件培养基是否可以重新承载MSCCOTα的影响。小鼠骨髓(BM)通过施用BASULFAN和环磷酰胺(BU-CY) - 在BALB / C受体小鼠中的方案的施用部分消融。将从C57BL / 6小鼠分离的BM细胞(BMC)通过尾静脉移植,具有或不含扁桃体衍生的MSC调节培养基(T-MSC CM)。当T-MSC cm或重组人类磷酸盐蛋白(RHPTN),从血液缺陷功能中的T-MSC分泌的细胞因子,用BMC注入时,股骨组织学分析显示出增加的BM细胞性增加。在用Bu-Cy调理方案治疗后观察Mesenteric和BM血管内皮细胞(ECS)的微观结构损伤;然而,T-MSC CM或RHPTN处理恢复了缺陷。在抗PTN抗体存在下,通过T-MSC CM的这些效果被破坏,表明PTN是EC恢复和增强的BM植入的关键介体。总之,T-MSC CM施用增强了BM植入,部分通过PTN生产恢复脉管系统。这些发现突出了T-MSC cm对增加HSC移植疗效的潜在治疗相关性。

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