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Insulin secretion assays in an engineered MIN6 cell line

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 measur...

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Detalles Bibliográficos
Autores principales: Yang, Liu, Chen, Wenbiao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9883224/
https://www.ncbi.nlm.nih.gov/pubmed/36718202
http://dx.doi.org/10.1016/j.mex.2023.102029
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author Yang, Liu
Chen, Wenbiao
author_facet Yang, Liu
Chen, Wenbiao
author_sort Yang, Liu
collection PubMed
description 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. • A highly glucose responsive beta cell reporter line (MIN6-6) with multiple engineered functionalities. • Allows for CRISPR/Cas9 mutagenesis, quantification of bulk insulin secretion by a straightforward nanoLuc assay and visualization of intracellular insulin granules. • Allows for en masse quantification of insulin granule exocytosis in individual cells under multiple conditions.
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spelling pubmed-98832242023-01-29 Insulin secretion assays in an engineered MIN6 cell line Yang, Liu Chen, Wenbiao MethodsX Method Article 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. • A highly glucose responsive beta cell reporter line (MIN6-6) with multiple engineered functionalities. • Allows for CRISPR/Cas9 mutagenesis, quantification of bulk insulin secretion by a straightforward nanoLuc assay and visualization of intracellular insulin granules. • Allows for en masse quantification of insulin granule exocytosis in individual cells under multiple conditions. Elsevier 2023-01-20 /pmc/articles/PMC9883224/ /pubmed/36718202 http://dx.doi.org/10.1016/j.mex.2023.102029 Text en © 2023 The Authors. Published by Elsevier B.V. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Method Article
Yang, Liu
Chen, Wenbiao
Insulin secretion assays in an engineered MIN6 cell line
title Insulin secretion assays in an engineered MIN6 cell line
title_full Insulin secretion assays in an engineered MIN6 cell line
title_fullStr Insulin secretion assays in an engineered MIN6 cell line
title_full_unstemmed Insulin secretion assays in an engineered MIN6 cell line
title_short Insulin secretion assays in an engineered MIN6 cell line
title_sort insulin secretion assays in an engineered min6 cell line
topic Method Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9883224/
https://www.ncbi.nlm.nih.gov/pubmed/36718202
http://dx.doi.org/10.1016/j.mex.2023.102029
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