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Reconstruction of Hematopoietic Inductive Microenvironment after Transplantation of VCAM-1-Modified Human Umbilical Cord Blood Stromal Cells

机译:移植VCam-1修饰人脐血基质细胞造血后诱导微环境的重建

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摘要

The hematopoietic inductive microenvironment (HIM) is where hematopoietic stem/progenitor cells grow and develop. Hematopoietic stromal cells were the key components of the HIM. In our previous study, we had successfully cultured and isolated human cord blood–derived stromal cells (HUCBSCs) and demonstrated that they could secret hemopoietic growth factors such as GM-CSF, TPO, and SCF. However, it is still controversial whether HUCBSCs can be used for reconstruction of HIM. In this study, we first established a co-culture system of HUCBSCs and cord blood CD34+ cells and then determined that using HUCBSCs as the adherent layer had significantly more newly formed colonies of each hematopoietic lineage than the control group, indicating that HUCBSCs had the ability to promote the proliferation of hematopoietic stem cells/progenitor cells. Furthermore, the number of colonies was significantly higher in vascular cell adhesion molecule-1 (VCAM-1)-modified HUCBSCs, suggesting that the ability of HUCBSCs in promoting the proliferation of hematopoietic stem cells/progenitor cells was further enhanced after having been modified with VCAM-1. Next, HUCBSCs were infused into a radiation-damaged animal model, in which the recovery of hematopoiesis was observed. The results demonstrate that the transplanted HUCBSCs were “homed in” to bone marrow and played roles in promoting the recovery of irradiation-induced hematopoietic damage and repairing HIM. Compared with the control group, the HUCBSC group had significantly superior effectiveness in terms of the recovery time for hemogram and myelogram, CFU-F, CFU-GM, BFU-E, and CFU-Meg. Such differences were even more significant in VCAM-1-modified HUCBSCs group. We suggest that HUCBSCs are able to restore the functions of HIM and promote the recovery of radiation-induced hematopoietic damage. VCAM-1 plays an important role in supporting the repair of HIM damage.
机译:造血诱导微环境(他)是造血干燥/祖细胞生长和发展的影响。造血基质细胞是他的关键组成部分。在我们以前的研究中,我们成功地培养和分离出人脐带血源性基质细胞(HUCBSC)并证明它们可以抵抗血液发作生长因子,如GM-CSF,TPO和SCF。然而,它仍然存在争议,无论HUCBSC是否可用于重建他。在这项研究中,我们首先建立了Hucbscs和脐带血CD34 + 细胞的共培养系统,然后确定使用Hucbscs作为粘附层的每种造血谱系的菌落明显多于控制组,表明Hucbscs具有促进造血干细胞/祖细胞的增殖的能力。此外,血管细胞粘附分子-1(VCAM-1) - 制定的HUCBSC中菌落的数量显着较高,表明HucBSC在改变后进一步提高了培养皿在促进造血干细胞/祖细胞的增殖中的能力vcam-1。接下来,HucBSC被注入到辐射受损的动物模型中,其中观察到血缺陷的回收率。结果表明将移植的HucBSC“归还”骨髓,并在促进辐照造血损伤和修复他的作用方面发挥作用。与对照组相比,HUCBSC组在血液图和髓正面,CFU-F,CFU-GM,BFU-E和CFU-MEG的恢复时间方面具有显着优越的效果。在VCAM-1改性的HUCBSCS组中,这种差异甚至更显着。我们建议Hucbscs能够恢复他的功能,并促进辐射诱导的造血损伤的复苏。 VCAM-1在支持他的修复方面发挥着重要作用。

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