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DUOC‐01, a Cell Therapy Product Derived from Human Cord Blood, Accelerates Remyelination

机译:Duoc-01,源自人脐带血的细胞疗法产品,加速重新髓鞘

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We developed a cell therapy product, DUOC-01, derived frombanked human umbilical cord blood, to treat demyelinatingconditions in the central nervous system. Previously, we demonstratedthat DUOC-01 increased myelination and decreasedgliosis and cellular infiltration in the corpus callosum ofimmune-incompetent mice treated with cuprizone. To investigatethe mechanism and test whether DUOC-01 will be efficaciousin other models of demyelination, we tested DUOC-01in lysophosphatidylcholine (LPC) demyelinated murine organotypiccerebellar brain slices and a mouse model of experimentalautoimmune encephalomyelitis (EAE). In the cerebellarbrain slice culture model, we found that DUOC-01 treatmentenhanced remyelination of LPC-mediated demyelinated neuronscompared with the untreated control samples. Thesedata demonstrate that DUOC-01 is capable of accelerating theremyelination of neurons by reducing gliosis and promotingoligodendrocyte proliferation and promoting myelin debrisclearance. Currently, we are testing the ability of DUOC-01 tolimit inflammation in EAE. Also, we are analyzing single cellsequencing data to determine various populations present inDUOC-01 cultures and to understand the functional pathwaysresponsible for promoting remyelination. Overall, our datasuggest that DUOC-01 could be beneficial in treating demyelinatingconditions.
机译:我们开发了一种细胞疗法产品,Duoc-01,源自营养的人脐血,以治疗中枢神经系统的脱霉素。以前,我们证明了Duoc-01增加了用Cupune-Themuntodent小鼠的胼calloSum中的髓鞘导出和减少凝集和细胞浸润。对调查机制和测试是否将DuoC-01脱髓脱髓鞘的其他模型,我们测试了Duoc-01荧光磷脂酰胆碱(LPC)脱髓鞘鼠有机型细胞脑切片和实验性造影脑膜炎(EAE)的小鼠模型。在小脑切片培养模型中,我们发现Duoc-01治疗LPC介导的脱髓鞘神经元与未处理的对照样品的治疗结果。 TheseData表明Duoc-01通过降低神经症和促进oligodendrocyte细胞增殖并促进髓鞘脱核来加速神经元的特征。目前,我们正在测试Duoc-01 Tolimit炎症在EAE中的能力。此外,我们正在分析单个细胞序列数据以确定各种群体呈现Induoc-01培养物,并了解促进核髓的功能性途径。总的来说,我们的Duoc-01可以有利于治疗DemyelinationConditions。

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