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TGF-β1 在 Notch 1 敲低兔骨髓间充质干细胞中诱导出类髓核细胞表型。

TGF-β1 induces a nucleus pulposus-like phenotype in Notch 1 knockdown rabbit bone marrow mesenchymal stem cells.

机构信息

Tongji Medical College, Union Hospital, Huazhong University of Science and Technology, Wuhan 430022, China.

出版信息

Cell Biol Int. 2013 Aug;37(8):820-5. doi: 10.1002/cbin.10109. Epub 2013 Apr 18.

Abstract

We have investigated the effects of Notch1 knockdown and treatment with TGF-β1 on the regulation of the directional differentiation of mesenchymal stem cells (MSCs). MSCs were isolated from the femur bone of New Zealand rabbits and purified by using discontinuous gradient density centrifugation. Notch1 siRNAs were designed, synthesised and transiently transfected into these MSCs, and treated with TGF-β1. The MSCs were examined for morphology, stained with toluidine blue for proteoglycan analysis and gene and protein expression were measured with qRT-PCR and Western blotting respectively. They had an ellipse or fusiform shape and gathered in nests or swirls after being cultured for 7 days. Notch1 expression was knocked down with Notch1 siRNA (the silence rate was 47%; P < 0.001). After knockdown and TGF-β1 treatment, MSCs expressed more proteoglycan (P < 0.01), and higher levels of collagen II mRNA and protein than control cells (P < 0.001). Thus knockdown of Notch1 expression in MSCs may be useful in the treatment of intervertebral disc degeneration.

摘要

我们研究了 Notch1 敲低和 TGF-β1 处理对间充质干细胞(MSCs)定向分化调控的影响。MSCs 从新西兰兔股骨中分离出来,并通过不连续梯度密度离心进行纯化。设计、合成 Notch1 siRNA 并瞬时转染到这些 MSCs 中,并进行 TGF-β1 处理。观察 MSCs 的形态,甲苯胺蓝染色进行蛋白聚糖分析,并用 qRT-PCR 和 Western blot 分别测量基因和蛋白表达。培养 7 天后,它们呈椭圆形或梭形,并聚集在巢或漩涡中。Notch1 siRNA 敲低 Notch1 表达(沉默率为 47%;P<0.001)。敲低 Notch1 表达和 TGF-β1 处理后,MSCs 表达更多的蛋白聚糖(P<0.01),以及更高水平的 II 型胶原 mRNA 和蛋白(P<0.001),与对照组细胞相比。因此,MSCs 中 Notch1 表达的敲低可能有助于治疗椎间盘退变。

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