Abstract

The Ca2+ modulated pulsatile glucagon and insulin secretions by pancreatic α and β cells play a crucial role in glucose homeostasis. However, how α and β cells coordinate to produce various Ca2+ oscillation patterns is still elusive. Using a microfluidic device and transgenic mice, we recorded Ca2+ signals from islet α and β cells, and observed heterogeneous Ca2+ oscillation patterns intrinsic to each islet. After a brief period of glucose stimulation, α and β cells’ oscillations were globally phase-locked. While the activation of α cells displayed a fixed time delay of ~20 s to that of β cells, β cells activated with a tunable period. Moreover, islet α cell number correlated with oscillation frequency. We built a mathematical model of islet Ca2+ oscillation incorporating paracrine interactions, which quantitatively agreed with the experimental data. Our study highlights the importance of cell-cell interaction in generating stable but tunable islet oscillation patterns.

The Ca2+ modulated pulsatile glucagon and insulin secretions by pancreatic α and β cells are critical in glucose homeostasis. Here the authors show that the Ca2+ oscillations of α and β cells are phase-locked, and that the oscillation pattern is tuned by paracrine interactions between α and β cells.

Details

Title
Pancreatic α and β cells are globally phase-locked
Author
Ren, Huixia 1   VIAFID ORCID Logo  ; Li, Yanjun 2 ; Han, Chengsheng 3 ; Yu, Yi 4 ; Shi, Bowen 5 ; Peng, Xiaohong 3 ; Zhang, Tianming 6 ; Wu, Shufang 4 ; Yang, Xiaojing 1 ; Kim, Sneppen 7   VIAFID ORCID Logo  ; Chen, Liangyi 8   VIAFID ORCID Logo  ; Tang, Chao 1   VIAFID ORCID Logo 

 Peking University, Center for Quantitative Biology, Beijing, China (GRID:grid.11135.37) (ISNI:0000 0001 2256 9319); Peking University, Peking-Tsinghua Center for Life Sciences, Beijing, China (GRID:grid.11135.37) (ISNI:0000 0001 2256 9319) 
 Peking University, Center for Quantitative Biology, Beijing, China (GRID:grid.11135.37) (ISNI:0000 0001 2256 9319); Peking University, Institute of Molecular Medicine, School of Future Technology, National Biomedical Imaging Center, Beijing, China (GRID:grid.11135.37) (ISNI:0000 0001 2256 9319) 
 Peking University, Institute of Molecular Medicine, School of Future Technology, National Biomedical Imaging Center, Beijing, China (GRID:grid.11135.37) (ISNI:0000 0001 2256 9319) 
 Peking University, Center for Quantitative Biology, Beijing, China (GRID:grid.11135.37) (ISNI:0000 0001 2256 9319) 
 Peking University, Peking-Tsinghua Center for Life Sciences, Beijing, China (GRID:grid.11135.37) (ISNI:0000 0001 2256 9319) 
 Peking University, Yuanpei College, Beijing, China (GRID:grid.11135.37) (ISNI:0000 0001 2256 9319) 
 University of Copenhagen, Niels Bohr Institute, Copenhagen, Denmark (GRID:grid.5254.6) (ISNI:0000 0001 0674 042X) 
 Peking University, Peking-Tsinghua Center for Life Sciences, Beijing, China (GRID:grid.11135.37) (ISNI:0000 0001 2256 9319); Peking University, Institute of Molecular Medicine, School of Future Technology, National Biomedical Imaging Center, Beijing, China (GRID:grid.11135.37) (ISNI:0000 0001 2256 9319) 
Publication year
2022
Publication date
2022
Publisher
Nature Publishing Group
e-ISSN
20411723
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
2681635211
Copyright
© The Author(s) 2022. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.