Literature DB >> 11812743

Overexpression of the Na/Ca exchanger shapes stimulus-induced cytosolic Ca(2+) oscillations in insulin-producing BRIN-BD11 cells.

Françoise Van Eylen1, Oscar Diaz Horta, Aurore Barez, Adama Kamagate, Peter R Flatt, Regina Macianskiene, Kanigula Mubagwa, André Herchuelz.   

Abstract

In response to glucose, mouse beta-cells display slow oscillations of the membrane potential and cytosolic free Ca(2+) concentration ([Ca(2+)](i)), whereas rat beta-cells display a staircase increase in these parameters. Mouse and rat islet cells differ also by their level of Na/Ca exchanger (NCX) activity. The view that the inward current generated by Na/Ca exchange shapes stimulus-induced electrical activity and [Ca(2+)](i) oscillations in pancreatic beta-cells was examined in insulin-producing BRIN-BD11 cells overexpressing the Na/Ca exchanger. BRIN-BD11 cells were stably transfected with NCX1.7, one of the exchanger isoforms identified in the beta-cell. Overexpression could be assessed at the mRNA and protein level. Appropriate targeting to the plasma membrane could be assessed by microfluorescence and the increase in Na/Ca exchange activity. In response to K(+), overexpressing cells showed a more rapid increase in [Ca(2+)](i) on membrane depolarization as well as a more rapid decrease of [Ca(2+)](i) on membrane repolarization. In response to glucose and tolbutamide, control BRIN cells showed large amplitude [Ca(2+)](i) oscillations. In contrast, overexpressing cells showed a staircase increase in [Ca(2+)](i) without such large oscillations. Diazoxide-induced membrane hyperpolarization restored large amplitude [Ca(2+)](i) oscillations in overexpressing cells. The present data confirm that Na/Ca exchange plays a significant role in the rat beta-cell [Ca(2+)](i) homeostasis, the exchanger being a versatile system allowing both Ca(2+) entry and outflow. Our data suggest that the current generated by the exchanger shapes stimulus-induced membrane potential and [Ca(2+)](i) oscillations in insulin-secreting cells, with the difference in electrical activity and [Ca(2+)](i) behavior seen in mouse and rat beta-cells resulting in part from a difference in Na/Ca exchange activity between these two cells.

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Year:  2002        PMID: 11812743     DOI: 10.2337/diabetes.51.2.366

Source DB:  PubMed          Journal:  Diabetes        ISSN: 0012-1797            Impact factor:   9.461


  5 in total

1.  Pancreatic β-cell Na+ channels control global Ca2+ signaling and oxidative metabolism by inducing Na+ and Ca2+ responses that are propagated into mitochondria.

Authors:  Iulia I Nita; Michal Hershfinkel; Chase Kantor; Guy A Rutter; Eli C Lewis; Israel Sekler
Journal:  FASEB J       Date:  2014-04-09       Impact factor: 5.191

2.  Inhibition of beta-cell sodium-calcium exchange enhances glucose-dependent elevations in cytoplasmic calcium and insulin secretion.

Authors:  Kevin S C Hamming; Daniel Soliman; Nicola J Webster; Gavin J Searle; Laura C Matemisz; David A Liknes; Xiao-Qing Dai; Thomas Pulinilkunnil; Michael J Riedel; Jason R B Dyck; Patrick E Macdonald; Peter E Light
Journal:  Diabetes       Date:  2010-04-22       Impact factor: 9.461

3.  Splice variant-dependent regulation of beta-cell sodium-calcium exchange by acyl-coenzyme As.

Authors:  Kevin S C Hamming; Michael J Riedel; Daniel Soliman; Laura C Matemisz; Nicola J Webster; Gavin J Searle; Patrick E MacDonald; Peter E Light
Journal:  Mol Endocrinol       Date:  2008-07-17

4.  Overexpression of the malate-aspartate NADH shuttle member Aralar1 in the clonal beta-cell line BRIN-BD11 enhances amino-acid-stimulated insulin secretion and cell metabolism.

Authors:  Katrin Bender; Pierre Maechler; Neville H McClenaghan; Peter R Flatt; Philip Newsholme
Journal:  Clin Sci (Lond)       Date:  2009-09-01       Impact factor: 6.124

Review 5.  Roles of Na+/Ca2+ exchanger 1 in digestive system physiology and pathophysiology.

Authors:  Qiu-Shi Liao; Qian Du; Jun Lou; Jing-Yu Xu; Rui Xie
Journal:  World J Gastroenterol       Date:  2019-01-21       Impact factor: 5.742

  5 in total

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