Membrane Potential and Calcium Dynamics in Beta Cells from Mouse Pancreas Tissue Slices: Theory, Experimentation, and Analysis

Sensors

Jurij Dolenšek¹  Denis Špelič²  Maša Skelin Klemen¹  Borut Žalik²  Marko Gosak¹  Marjan Slak Rupnik¹  Andraž Stožer¹ 

[1] Institute of Physiology, Faculty of Medicine, University of Maribor, SI-2000 Maribor, Slovenia; E-Mails:;Faculty of Electrical Engineering and Computer Science, University of Maribor, SI-2000 Maribor, Slovenia; E-Mails:

关键词: calcium sensors;    membrane potential sensors;    calcium imaging;    membrane potential imaging;    beta cell;    pancreas;    denoising;    patch-clamp;   

DOI  :  10.3390/s151127393

来源: mdpi

【 摘 要 】

Beta cells in the pancreatic islets of Langerhans are precise biological sensors for glucose and play a central role in balancing the organism between catabolic and anabolic needs. A hallmark of the beta cell response to glucose are oscillatory changes of membrane potential that are tightly coupled with oscillatory changes in intracellular calcium concentration which, in turn, elicit oscillations of insulin secretion. Both membrane potential and calcium changes spread from one beta cell to the other in a wave-like manner. In order to assess the properties of the abovementioned responses to physiological and pathological stimuli, the main challenge remains how to effectively measure membrane potential and calcium changes at the same time with high spatial and temporal resolution, and also in as many cells as possible. To date, the most wide-spread approach has employed the electrophysiological patch-clamp method to monitor membrane potential changes. Inherently, this technique has many advantages, such as a direct contact with the cell and a high temporal resolution. However, it allows one to assess information from a single cell only. In some instances, this technique has been used in conjunction with CCD camera-based imaging, offering the opportunity to simultaneously monitor membrane potential and calcium changes, but not in the same cells and not with a reliable cellular or subcellular spatial resolution. Recently, a novel family of highly-sensitive membrane potential reporter dyes in combination with high temporal and spatial confocal calcium imaging allows for simultaneously detecting membrane potential and calcium changes in many cells at a time. Since the signals yielded from both types of reporter dyes are inherently noisy, we have developed complex methods of data denoising that permit for visualization and pixel-wise analysis of signals. Combining the experimental approach of high-resolution imaging with the advanced analysis of noisy data enables novel physiological insights and reassessment of current concepts in unprecedented detail.

【 授权许可】

CC BY   
© 2015 by the authors; licensee MDPI, Basel, Switzerland.