Insulin secretion from pancreatic beta cells is crucial for maintaining glucose homeostasis. The murine insulinoma derived MIN6 cell line is commonly used as a model for insulin secretion studies. However, its glucose responsiveness wanes with passaging, and insulin secretion is traditionally measured by expensive and time-consuming RIA or ELISA. We have developed a MIN6 subclone (MIN6-6) that allows for high throughput assay of insulin secretion in both population and single cells. In addition, MIN6-6 also expresses Cas9, permitting genome wide CRISPR screen of insulin secretion using a pooled sgRNA library. Here we provide methods for assaying insulin secretion both in bulk and in single cells in MIN6-6 cells, as well as for CRISPR screen of insulin secretion.â¢A highly glucose responsive beta cell reporter line (MIN6-6) with multiple engineered functionalities.â¢Allows for CRISPR/Cas9 mutagenesis, quantification of bulk insulin secretion by a straightforward nanoLuc assay and visualization of intracellular insulin granules.â¢Allows for en masse quantification of insulin granule exocytosis in individual cells under multiple conditions.
Insulin secretion assays in an engineered MIN6 cell line.
在工程化MIN6细胞系中进行胰岛素分泌测定
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作者:Yang Liu, Chen Wenbiao
| 期刊: | MethodsX | 影响因子: | 1.900 |
| 时间: | 2023 | 起止号: | 2023 Jan 20; 10:102029 |
| doi: | 10.1016/j.mex.2023.102029 | 研究方向: | 细胞生物学 |
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