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The Reparative Effects of Human Adipose-Derived Mesenchymal Stem Cells in the Chemotherapy-Damaged Thymus

机译:人脂肪衍生间充质干细胞在化疗受损胸腺中的重复效应

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Hematological patients who accept chemotherapy always develop secondary tumor or even die of severe infections. As an important central lymphoid organ, the thymus is frequently damaged during chemotherapy. Previous studies showed that the mesenchymal stem cells (MSCs) can promote the proliferation and repair of epithelial cells in thymus. The purpose of our study is to investigate the reparative effects of human adipose-derived mesenchymal stem cells (hADMSCs) in chemotherapy-treated damaged thymus. Eighty mice were randomly divided into four groups: normal group, model control group, hADMSCs untreated group, and hADMSCs treated group. The mice were injected intraperitoneally with dexamethasone sodium phosphate (Dex 20 mg/kg), except the normal group. Then, the chemotherapy models were obtained after 1 week; the treated group was infused intraperitoneally with hADMSCs, whereas the model control group was injected with equal volumes of normal saline. The hADMSC's infusion day was regarded as day 0. The mice were sacrificed at different time points (days 3, 7, 10, and 14). The pathological structure and the function of the thymus, the recovery of T-lymphocyte subpopulation, and the proportion of regulatory T (Treg) cells in spleen and peripheral blood were detected. Additionally, we transfected hADMSCs by lentivirus with green fluorescent protein (GFP) to confirm whether they home to thymus and detected the expressions of cytokines that are associated with the development of thymus in hADMSCs and thymus. The results of the study showed that the hADMSCs treated group had a more rapid recovery in terms of thymic pathological structure and function. The hADMSCs could home to the damaged thymus and secrete cytokines that played important roles in repairing damaged thymus. The results indicated that hADMSCs could repair the damaged thymus caused by chemotherapy and improve the immune microenvironment, which may be a potential treatment for hematological patients.
机译:接受化疗的血液学患者总是开发次要肿瘤甚至死于严重的感染。作为重要的中央淋巴管器官,胸腺经常在化疗期间受损。以前的研究表明,间充质干细胞(MSCs)可以促进胸腺中上皮细胞的增殖和修复。我们研究的目的是探讨人脂肪衍生的间充质干细胞(HADMSCs)在化疗处理的受损胸腺中的重复影响。将80只小鼠随机分为四组:正常组,模型对照组,HADMSCs未处理组,以及HADMSCS治疗组。除正常组外,将小鼠用磷酸钠(DEX 20mg / kg)腹膜内注射。然后,1周后获得化疗模型;治疗组用HADMSCs腹膜内注入,而模型对照组以相同的正常盐水注射。 HADMSC的输注日被认为是第0天。在不同时间点(第3,7,10和14天)处死小鼠。检测到病理结构和胸腺的函数,T淋巴细胞亚化群的回收,以及脾脏和外周血中的调节性T(Treg)细胞的比例。此外,我们通过慢病毒转染患有绿色荧光蛋白(GFP)的HADMSC,以确认它们是否回到胸腺中并检测到与哈姆森和胸腺胸腺发育相关的细胞因子的表达。该研究的结果表明,在胸腺病理结构和功能方面,HADMSCS治疗组在较快的恢复。 HADMSCs可以在家中受损胸腺和分泌细胞因子,这些细胞因子在修复受损胸腺中发挥了重要作用。结果表明,HADMSCs可以修复由化疗引起的受损胸腺,并改善免疫微环境,这可能是血液学患者的潜在治疗方法。

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