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A Systems Biology Approach to Understand the Association between Gut MIcrobiota and Malnutrition

机译:理解肠道微生物群与营养不良之间关联的系统生物学方法

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Liver tissue demand is escalating due to the greatly increasing incidence of liver disease.We hypothesize that the structures and cues that initiate 3D liver formation can be mimicked with human pluripotent stem cells(hPSC).Thus we aimed to engineer an in vitro model of the liver diverticulum(LD),a key structure that: 1)arises in mouse development(E9.5)and human development(d26)and 2)forms the 3D liver.From inside the gut to outside,the LD is composed of a single layer of hepatic endoderm(HE),encased by a single layer of endothelial cells,and surrounded by the septum transversum mesenchyme(STM).3D liver formation starts when the hepatic endoderm(HE)delaminates,joins with the endothelial cells,and migrates into the STM.We first determined the appropriate LD dimensions with an online mouse database.
机译:由于肝脏疾病的发生率大大增加,肝组织需求升高。我们假设启动3D肝脏形成的结构和提示可以用人多能干细胞(HPSC)模仿.Thus我们的目标是工程师的体外模型 肝憩室(LD),一个关键结构:1)在小鼠开发(E9.5)中出现(E9.5)和人类发展(D26)和2)形成3D肝脏。从肠道内部到外部,LD由单个组成 由单层内皮细胞包封的肝内胚层(HE)层,并被隔膜跨越间能(STM).3D肝脏形成开始,当肝内胚层(HE)分层,与内皮细胞连接并迁移到 STM.WE首先使用在线鼠标数据库确定适当的LD维度。

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