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Forming cell cluster regulates glucose-stimulated insulin gene expression and promotes insulin secretion in pancreatic beta cell

机译:形成细胞聚类调节葡萄糖刺激的胰岛素基因表达,并促进胰岛素β细胞中的胰岛素分泌

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In summary, the formation of pancreatic β-cell spheroids influence the insulin gene expression. Relative to monolayer, clusters has higher stimulation-index and lower constitutive insulin release. Besides, Cx36 protein plays an important role in the regulating pathway. In low glucose condition, the RNA expressions of clusters showed that most genes previously activated in monolayers were downregulated. The expressions of Ins1, Pdx1 and MafA were further upregulated for clusters under high glucose environment. This study reveals that cell coupling regulates glucose-stimulated insulin gene expression to promote insulin secretion in mouse β-cells. Moreover, cell aggregation also enhances in vivo performance of β-cells.
机译:总之,胰腺β-细胞球体的形成影响了胰岛素基因表达。相对于单层,簇具有较高的刺激指数和较低的组成胰岛素释放。此外,CX36蛋白在调节途径中起重要作用。在低血糖条件下,簇的RNA表达表明,最先前在单层中活化的大多数基因被下调。在高葡萄糖环境下,进一步上调INS1,PDX1和MAFA的表达。本研究表明,细胞偶联调节葡萄糖刺激的胰岛素基因表达,以促进小鼠β细胞中的胰岛素分泌。此外,细胞聚集也增强了β细胞的体内性能。

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