Cellular communication and heterogeneity in pancreatic islet insulin secretion dynamics

被引:109
作者
Benninger, Richard K. P. [1 ,2 ]
Piston, David W. [3 ]
机构
[1] Univ Colorado, Dept Bioengn, Aurora, CO 80045 USA
[2] Univ Colorado, Barbara Davis Ctr, Aurora, CO USA
[3] Vanderbilt Univ, Dept Mol Physiol & Biophys, Nashville, TN 37235 USA
关键词
islet of Langerhans; microscopy; fluorescence; computer modeling; calcium waves; MOUSE BETA-CELLS; PULSATILE INSULIN; B-CELLS; LIMITED COORDINATION; CYTOPLASMIC CA2+; GAP-JUNCTIONS; GLUCOSE; OSCILLATIONS; LANGERHANS; RELEASE;
D O I
10.1016/j.tem.2014.02.005
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Coordinated pulses of electrical activity and insulin secretion are a hallmark of the islet of Langerhans. These coordinated behaviors are lost when beta cells are dissociated, which also leads to increased insulin secretion at low glucose levels. Islets without gap junctions exhibit asynchronous electrical activity similar to dispersed cells, but their secretion at low glucose levels is still clamped off, putatively by a juxtacrine mechanism. Mice lacking beta cell gap junctions have near-normal average insulin levels, but are glucose intolerant due to reduced first-phase and pulsatile insulin secretion, illustrating the importance of temporal dynamics. Here, we review the quantitative data on islet synchronization and the current mathematical models that have been developed to explain these behaviors and generate greater understanding of the underlying mechanisms.
引用
收藏
页码:399 / 406
页数:8
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