The effects of beta-cell mass and function, intercellular coupling, and islet synchrony on $\textrm{Ca}^{2+}$ dynamics

TL;DR

This study uses a comprehensive electrophysiological model to explore how beta-cell mass, intercellular coupling, and islet synchrony influence calcium dynamics and insulin secretion in the context of type 2 diabetes, highlighting electrical coupling's critical role.

Contribution

The paper introduces a detailed electrophysiological model of human beta-cell clusters to analyze the impact of cell mass, coupling, and synchrony on calcium dynamics and insulin secretion in T2D.

Findings

Beta-cell mass defect impairs intra-islet synchrony and alters calcium oscillations.

Electrical coupling plays a more significant role than metabolic coupling in islet function.

Modulating potassium channel conductance affects calcium oscillations and insulin secretion.

Abstract

Type 2 diabetes (T2D) is a challenging metabolic disorder characterized by a substantial loss of $\beta$-cell mass and alteration of $\beta$-cell function in the islets of Langerhans, disrupting insulin secretion and glucose homeostasis. The mechanisms for deficiency in $\beta$-cell mass and function during the hyperglycemia development and T2D pathogenesis are complex. To study the relative contribution of $\beta$-cell mass to $\beta$-cell function in T2D, we make use of a comprehensive electrophysiological model of human $\beta$-cell clusters. We find that defect in $\beta$-cell mass causes a functional decline in single $\beta$-cell, impairment in intra-islet synchrony, and changes in the form of oscillatory patterns of membrane potential and intracellular $\textrm{Ca}^{2+}$ concentration, which can lead to changes in insulin secretion dynamics and in insulin levels. The model demonstrates a good correspondence between suppression of synchronizing electrical activity and published experimental measurements. We then compare the role of gap junction-mediated electrical coupling with both $\beta$-cell synchronization and metabolic coupling in the behavior of $\textrm{Ca}^{2+}$ concentration dynamics within human islets. Our results indicate that inter-$\beta$-cellular electrical coupling depicts a more important factor in shaping the physiological regulation of islet function and in human T2D. We further predict that varying the whole-cell conductance of delayed rectifier $\textrm{K}^{+}$ channels modifies oscillatory activity patterns of $\beta$-cell population lacking intercellular coupling, which significantly affect $\textrm{Ca}^{2+}$ concentration and insulin secretion.