Summary
We describe a technique using normal and diabetic (dbdb) mice to establish primary pancreatic cultures that spread and assume a characteristic epithelial morphology. These cultures contain 4 to 7% beta cells, secrete insulin in response to stimuli for 10 to 14 d, contain few fibroblasts, and have a cell viability that is greater than 95%. The cells attach firmly to glass cover slips and are ideal for the study of insulin secretory granules or contractile proteins using indirect immunofluorescence.
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Bolton, W.E., Terrell, S.P., Andrews, K.L. et al. Preparation of primary monolayer cultures of mouse pancreatic epithelial cells. Journal of Tissue Culture Methods 7, 39–42 (1982). https://doi.org/10.1007/BF01666879
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DOI: https://doi.org/10.1007/BF01666879