Optogenetic β cell interrogation in vivo reveals a functional hierarchy directing the Ca 2+ response to glucose supported by vitamin B6

Author:

Delgadillo-Silva Luis Fernando123ORCID,Tasöz Emirhan12ORCID,Singh Sumeet Pal4ORCID,Chawla Prateek1,Georgiadou Eleni5,Gompf Anne1,Rutter Guy A.356ORCID,Ninov Nikolay12ORCID

Affiliation:

1. Centre for Regenerative Therapies TU Dresden, Dresden 01307, Germany.

2. Paul Langerhans Institute Dresden of the Helmholtz Center Munich at the University Hospital Carl Gustav Carus of TU Dresden, German Center for Diabetes Research (DZD e.V.), Dresden 01307, Germany.

3. Cardiometabolic Axis, CR-CHUM, and University of Montreal, Montreal, QC, Canada; 1IRIBHM, Université Libre de Bruxelles (ULB), 1070 Brussels, Belgium.

4. IRIBHM, Université Libre de Bruxelles (ULB), Brussels, Belgium.

5. Section of Cell Biology and Functional Genomics, Division of Diabetes, Endocrinology and Metabolism, Faculty of Medicine, Department of Metabolism, Digestion and Reproduction, Faculty of Medicine, Imperial College London, Hammersmith Hospital, London W12 ONN, UK.

6. Lee Kong Chian School of Medicine, Nanyang Technological College, Singapore, Singapore.

Abstract

Coordination of cellular activity through Ca 2+ enables β cells to secrete precise quantities of insulin. To explore how the Ca 2+ response is orchestrated in space and time, we implement optogenetic systems to probe the role of individual β cells in the glucose response. By targeted β cell activation/inactivation in zebrafish, we reveal a hierarchy of cells, each with a different level of influence over islet-wide Ca 2+ dynamics. First-responder β cells lie at the top of the hierarchy, essential for initiating the first-phase Ca 2+ response. Silencing first responders impairs the Ca 2+ response to glucose. Conversely, selective activation of first responders demonstrates their increased capability to raise pan-islet Ca 2+ levels compared to followers. By photolabeling and transcriptionally profiling β cells that differ in their thresholds to a glucose-stimulated Ca 2+ response, we highlight vitamin B6 production as a signature pathway of first responders. We further define an evolutionarily conserved requirement for vitamin B6 in enabling the Ca 2+ response to glucose in mammalian systems.

Publisher

American Association for the Advancement of Science (AAAS)

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