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Characterization of a novel glucose-responsive insulin-secreting cell line, BRIN-BD11, produced by electrofusion

Biomedical Sciences Research Institute Computer Science Research Institute Environmental Sciences Research Institute Nanotechnology & Advanced Materials Research Institute

McClenaghan, Neville, Barnett, CR, AhSing, E, Abdel-Wahab, Yasser, O'Harte, Finbarr, Yoon, TW, SwanstonFlatt, SK and Flatt, Peter (1996) Characterization of a novel glucose-responsive insulin-secreting cell line, BRIN-BD11, produced by electrofusion. DIABETES, 45 (8). pp. 1132-1140. [Journal article]

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Abstract

A novel insulin-secreting cell line (BRIN-BD11) was established after electrofusion of RINm5F cells with New England Deaconess Hospital rat pancreatic islet cells, Wells of cell fusion mixture with insulin output 5-10 times greater than parent RINm5F cells were subcultured with eventual establishment of clones, including BRIN-BD11, Morphological studies established that these cells grow as monolayers with epithelioid characteristics, maintaining stability in tissue culture for >50 passages, Culture of these cells for 24 h at 5.6-33.3 mmol/l glucose revealed a 1.8- to 2.0-fold increase of insulin output compared with 1.4 mmol/l glucose, Dynamic insulin release was recorded in response to 16.7 mmol/l glucose, resulting in a rapid threefold insulin secretory peak followed by a sustained output slightly above basal, In acute 20-min tests, 4.2-16.7 mmol/l glucose evoked a stepwise two-to threefold stimulation of insulin release, 3-Isobutyl-1-methylxanthine (1 mmol/l) served to increase basal and glucose-stimulated insulin release, shifting the threshold from 4.4 to 1.1 mmol/l glucose, Stimulation of insulin secretion with 16.7 mmol/l glucose was abolished by manno-heptulose or diazoxide (15 or 0.5 mmol/l), In contrast, glyceraldehyde (10 mmol/l) and 25 mmol/l K+ evoked 1.7- to 9.0-fold insulin responses, L-Alanine (10 mmol/l) evoked a twofold secretory response, which was potentiated 1.4-fold by increasing the Ca2+ concentration from 1.28 to 7.68 mmol/l, Forskolin (25 mu mol/l) and phorbol 12-myristate 13-acetate (10 nmol/l) both increased insulin secretion in the presence of L-alanine (1.4- and 1.8-fold, respectively), Western blotting confirmed that BRIN-BD11 cells expressed the GLUT2 glucose transporter, This, coupled with a high glucokinase/hexokinase ratio in the cells, confirms an intact glucose sensing mechanism, High-performance liquid chromatography analysis demonstrated that insulin was the major product secreted under stimulatory conditions, Collectively, these data indicate that the BRIN-BD11 cell line represents an important stable glucose-responsive insulin secreting beta-cell line for future studies.

Item Type:Journal article
Faculties and Schools:Faculty of Life and Health Sciences
Faculty of Life and Health Sciences > School of Biomedical Sciences
Research Institutes and Groups:Biomedical Sciences Research Institute
Biomedical Sciences Research Institute > Diabetes
ID Code:3158
Deposited By:Professor Peter Flatt
Deposited On:08 Jan 2010 13:35
Last Modified:15 Jun 2011 11:10

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