Volume-sensitive amino acid efflux from a pancreatic β-cell line

2000 ◽  
Vol 162 (1-2) ◽  
pp. 201-208 ◽  
Author(s):  
A.C.G. Grant ◽  
J. Thomson ◽  
V.A. Zammit ◽  
D.B. Shennan
2011 ◽  
Vol 16 (5) ◽  
pp. 608-616 ◽  
Author(s):  
Manami Oya ◽  
Hideyuki Suzuki ◽  
Yuichiro Watanabe ◽  
Moritoshi Sato ◽  
Takashi Tsuboi

2013 ◽  
Vol 30 (1) ◽  
pp. 178-187 ◽  
Author(s):  
Marie Shinohara ◽  
Hiroshi Kimura ◽  
Kevin Montagne ◽  
Kikuo Komori ◽  
Teruo Fujii ◽  
...  

2013 ◽  
Vol 394 (7) ◽  
pp. 909-918 ◽  
Author(s):  
Srividya Vasu ◽  
Neville H. McClenaghan ◽  
Jane T. McCluskey ◽  
Peter R. Flatt

Abstract The novel insulin-secreting human pancreatic β-cell line, 1.1B4, demonstrates stability in culture and many of the secretory functional attributes of human pancreatic β-cells. This study investigated the cellular responses of 1.1B4 cells to lipotoxicity. Chronic 18-h exposure of 1.1B4 cells to 0.5 mm palmitate resulted in decreased cell viability and insulin content. Secretory responses to classical insulinotropic agents and cellular Ca2+ handling were also impaired. Palmitate decreased glucokinase activity and mRNA expression of genes involved in secretory function but up-regulated mRNA expression of HSPA5, EIF2A, and EIF2AK3, implicating activation of the endoplasmic reticulum stress response. Palmitate also induced DNA damage and apoptosis of 1.1B4 cells. These responses were accompanied by increased gene expression of the antioxidant enzymes SOD1, SOD2, CAT and GPX1. This study details molecular mechanisms underlying lipotoxicity in 1.1B4 cells and indicates the potential value of the novel β-cell line for future research.


1996 ◽  
Vol 71 ◽  
pp. 158
Author(s):  
Yasufimi Fukano ◽  
Tsuyoshi Azuma ◽  
Koichiro Ozawa ◽  
Jun-ichi Miyazaki ◽  
Tuntomu Masujima

1989 ◽  
Vol 1012 (1) ◽  
pp. 107-115 ◽  
Author(s):  
Jean-François Geschwind ◽  
Marcia Hiriart ◽  
Major C. Glennon ◽  
Habiba Najafi ◽  
Barbara E. Corkey ◽  
...  

Islets ◽  
2013 ◽  
Vol 5 (4) ◽  
pp. 170-177 ◽  
Author(s):  
Srividya Vasu ◽  
Neville H McClenaghan ◽  
Jane T McCluskey ◽  
Peter R Flatt

Cells ◽  
2020 ◽  
Vol 9 (5) ◽  
pp. 1129
Author(s):  
Chi Woo Yoon ◽  
Nan Sook Lee ◽  
Kweon Mo Koo ◽  
Sunho Moon ◽  
Kyosuk Goo ◽  
...  

In glucose-stimulated insulin secretion (GSIS) of pancreatic β-cells, the rise of free cytosolic Ca2+ concentration through voltage-gated calcium channels (VGCCs) triggers the exocytosis of insulin-containing granules. Recently, mechanically induced insulin secretion pathways were also reported, which utilize free cytosolic Ca2+ ions as a direct regulator of exocytosis. In this study, we aimed to investigate intracellular Ca2+ responses on the HIT-T15 pancreatic β-cell line upon low-intensity pulsed ultrasound (LIPUS) stimulation and found that ultrasound induces two distinct types of intracellular Ca2+ oscillation, fast-irregular and slow-periodic, from otherwise resting cells. Both Ca2+ patterns depend on the purinergic signaling activated by the rise of extracellular ATP or ADP concentration upon ultrasound stimulation, which facilitates the release through mechanosensitive hemichannels on the plasma membrane. Further study demonstrated that two subtypes of purinergic receptors, P2X and P2Y, are working in a competitive manner depending on the level of glucose in the cell media. The findings can serve as an essential groundwork providing an underlying mechanism for the development of a new therapeutic approach for diabetic conditions with further validation.


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