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Human mesenchymal stem cells differentiate to epithelial cells when cultured on thick collagen gel

机译:在厚胶原蛋白凝胶上培养时,人间充质干细胞分化为上皮细胞

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摘要

The stem cell niche is crucial to the control of stem cell fate determination in vitro as well as in vivo, and an understanding of these niches is required for the progression of stem cell and tissue engineering. The goal of our study was to commit human mesenchymal stem cells (hMSCs) to the epithelial lineage. To do this, we cultured bone marrow-derived mesenchymal stem cells (MSCs) on plates coated with type I collagen gel with or without 10 muM dll-trans retinoic acid (ATRA).We found depth-dependent differentiation of hMSCs to the epithelial lineage, with the thick collagen gel (1900 um) generating more than 80% cytokeratin-18 (CK-18)-positive cells, whereas the thin collagen gel (100 mum) generated significantly fewer CK-18-positive cells. In addition, we found that supplementation of 10 muM ATRA enhanced CK-18 expression and induced cluster-formation in cells grown on the thick collagen gel. The effect of gel depth on hMSC differentiation appears to be caused by partial cytoskeletal disruption.These results suggest that ATRA and a collagen extracellular matrix may have a synergistic effect on differentiation of human mesenchymal stem cells to epithelial lineage.
机译:干细胞的生态位对于控制体内和体外干细胞命运的决定至关重要,因此对干细胞和组织工程的进展需要了解这些壁ni。我们研究的目的是将人间充质干细胞(hMSCs)提交上皮细胞系。为此,我们在涂有或不带有10μMdll-反式视黄酸(ATRA)的I型胶原凝胶包被的板上培养骨髓源性间充质干细胞(MSCs)。我们发现hMSCs向上皮细胞系的深度依赖性分化,厚胶原蛋白凝胶(1900 um)产生80%的细胞角蛋白18(CK-18)阳性细胞,而薄胶原蛋白凝胶(100 mum)产生的CK-18阳性细胞明显更少。此外,我们发现,在厚胶原凝胶上生长的细胞中,添加10μMATRA可以增强CK-18表达并诱导簇形成。凝胶深度对hMSC分化的影响似乎是由部分细胞骨架破坏引起的。这些结果表明ATRA和胶原细胞外基质可能对人间充质干细胞向上皮细胞的分化具有协同作用。

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