Nurr1基因修饰人脐血间充质干细胞源性多巴胺能 神经元移植治疗帕金森病
【目的】 探讨Nurr1基因修饰的人脐血间充质干细胞(HUCB-MSC)源性的多巴胺能神经元移植对帕金森病(PD)模型鼠的治疗作用.【方法】 SD大鼠PD模型随机分为假手术组(A组)?单纯HUCB-MSC组(B组)、Nurr1基因修饰HUCB-MSC组(C组)。将HUCB-MSC及Nurr1基因修饰后的HUCB-MSC体外分化为多巴胺能神经元,并通过立体定向的手段将其移植入毁损侧纹状体,观察移植前后PD模型大鼠旋转行为的变化和脑内多巴胺(DA)含量的改变,以及纹状体区酪氨酸羟化酶 (TH) 表达的变化。【
doaj
[Human umbilical cord mesenchymal stem cells protect against neonatal white matter injury by activating the Nrf2/Keap1/HO-1 signaling pathway]. [PDF]
Wang C, Wang MX, Zhu YP.
europepmc +1 more source
[Chitosan hydrogel loaded with human umbilical cord mesenchymal stem cell-derived exosomes promotes healing of chronic diabetic wounds in rats]. [PDF]
Qiu X, Wang M, Tang J, Zhou J, Jin C.
europepmc +1 more source
[Human umbilical cord mesenchymal stem cell grafting alleviates inflammatory response in type 1 diabetic mice by suppressing M1 macrophage polarization through Chi3l1]. [PDF]
Liu X, Xu Y, Sheng H, Liu H.
europepmc +1 more source
[Application of umbilical cord mesenchymal stem cells in the treatment of severe immune-mediated thrombocytopenia after allogeneic hematopoietic stem cell transplantation in children]. [PDF]
Zhang B, Luan Z, Tang XF, Wu NH.
europepmc +1 more source
[Role of the nuclear factor-kappa B signaling pathway in the repair of white matter injury in neonatal rats through human umbilical cord mesenchymal stem cell transplantation]. [PDF]
Zhang SJ +4 more
europepmc +1 more source
[Immunomodulatory mechanism of umbilical cord mesenchymal stem cells modified by miR-125b-5p in systemic lupus erythematosus]. [PDF]
Wu Z +8 more
europepmc +1 more source
[Repair effect of different doses of human umbilical cord mesenchymal stem cells on white matter injury in neonatal rats]. [PDF]
Zhang J +5 more
europepmc +1 more source
[Successful treatment of a hepatitis B-related acute-on-chronic liver failure patient with adefovir dipivoxil combined with artificial liver and human umbilical mesenchymal stem cells]. [PDF]
Niu JJ, Wang F, Xin YN, Chen LZ.
europepmc +1 more source
Human umbilical cord mesenchymal stem cells attenuate diabetic nephropathy through the IGF1R-CHK2-p53 signalling axis in male rats with type 2 diabetes mellitus. [PDF]
Zhang H +16 more
europepmc +1 more source

