Molecular phenotyping of single pancreatic islet leader beta cells by "Flash-Seq"

Aims: Spatially-organized increases in cytosolic Ca2+ within pancreatic beta cells in the pancreatic islet underlie the stimulation of insulin secretion by high glucose. Recent data have revealed the existence of subpopulations of beta cells including “leaders” which initiate Ca2+ waves. Whether lea...

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Main Authors: Chabosseau, Pauline, Yong, Fiona, Delgadillo-Silva, Luis F., Lee, Eun Young, Melhem, Rana, Li, Shiying, Gandhi, Nidhi, Wastin, Jules, Noriega, Livia Lopez, Leclerc, Isabelle, Ali, Yusuf, Hughes, Jing W., Sladek, Robert, Martinez-Sanchez, Aida, Rutter, Guy A.
Other Authors: Lee Kong Chian School of Medicine (LKCMedicine)
Format: Article
Language:English
Published: 2023
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Online Access:https://hdl.handle.net/10356/171807
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spelling sg-ntu-dr.10356-1718072023-11-12T15:37:47Z Molecular phenotyping of single pancreatic islet leader beta cells by "Flash-Seq" Chabosseau, Pauline Yong, Fiona Delgadillo-Silva, Luis F. Lee, Eun Young Melhem, Rana Li, Shiying Gandhi, Nidhi Wastin, Jules Noriega, Livia Lopez Leclerc, Isabelle Ali, Yusuf Hughes, Jing W. Sladek, Robert Martinez-Sanchez, Aida Rutter, Guy A. Lee Kong Chian School of Medicine (LKCMedicine) Science::Medicine Diabetes Beta Cell Aims: Spatially-organized increases in cytosolic Ca2+ within pancreatic beta cells in the pancreatic islet underlie the stimulation of insulin secretion by high glucose. Recent data have revealed the existence of subpopulations of beta cells including “leaders” which initiate Ca2+ waves. Whether leader cells possess unique molecular features, or localisation, is unknown. Main methods: High speed confocal Ca2+ imaging was used to identify leader cells and connectivity analysis, running under MATLAB and Python, to identify highly connected “hub” cells. To explore transcriptomic differences between beta cell sub-groups, individual leaders or followers were labelled by photo-activation of the cryptic fluorescent protein PA-mCherry and subjected to single cell RNA sequencing (“Flash-Seq”). Key findings: Distinct Ca2+ wave types were identified in individual islets, with leader cells present in 73 % (28 of 38 islets imaged). Scale-free, power law-adherent behaviour was also observed in 29 % of islets, though “hub” cells in these islets did not overlap with leaders. Transcripts differentially expressed (295; padj < 0.05) between leader and follower cells included genes involved in cilium biogenesis and transcriptional regulation. Providing some support for these findings, ADCY6 immunoreactivity tended to be higher in leader than follower cells, whereas cilia number and length tended to be lower in the former. Finally, leader cells were located significantly closer to delta, but not alpha, cells in Euclidian space than were follower cells. Significance: The existence of both a discrete transcriptome and unique localisation implies a role for these features in defining the specialized function of leaders. These data also raise the possibility that localised signalling between delta and leader cells contributes to the initiation and propagation of islet Ca2+ waves. Published version G.R. was supported by a Wellcome Trust Investigator (212625/Z/ 18/Z) Award, MRC Programme grant (MR/R022259/1), and Diabetes UK (BDA/11/0004210, BDA/15/0005275, BDA 16/0005485) grants, start-up funds from the CRCHUM and a John R. Evans Leaders Award from Innovation Canada. This project has received funding from the European Union's Horizon 2020 research and innovation programme via the Innovative Medicines Initiative 2 Joint Undertaking under grant agreement No. 115881 (RHAPSODY) to G.R. I.L. was supported by a project grant from Diabetes UK (16/0005485). E.L. and J.H. were supported by NIH grants DK115795 and DK127748. 2023-11-08T05:10:52Z 2023-11-08T05:10:52Z 2023 Journal Article Chabosseau, P., Yong, F., Delgadillo-Silva, L. F., Lee, E. Y., Melhem, R., Li, S., Gandhi, N., Wastin, J., Noriega, L. L., Leclerc, I., Ali, Y., Hughes, J. W., Sladek, R., Martinez-Sanchez, A. & Rutter, G. A. (2023). Molecular phenotyping of single pancreatic islet leader beta cells by "Flash-Seq". Life Sciences, 316, 121436-. https://dx.doi.org/10.1016/j.lfs.2023.121436 0024-3205 https://hdl.handle.net/10356/171807 10.1016/j.lfs.2023.121436 36706832 2-s2.0-85147277582 316 121436 en Life Sciences © 2023 The Authors. Published by Elsevier Inc. This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). application/pdf
institution Nanyang Technological University
building NTU Library
continent Asia
country Singapore
Singapore
content_provider NTU Library
collection DR-NTU
language English
topic Science::Medicine
Diabetes
Beta Cell
spellingShingle Science::Medicine
Diabetes
Beta Cell
Chabosseau, Pauline
Yong, Fiona
Delgadillo-Silva, Luis F.
Lee, Eun Young
Melhem, Rana
Li, Shiying
Gandhi, Nidhi
Wastin, Jules
Noriega, Livia Lopez
Leclerc, Isabelle
Ali, Yusuf
Hughes, Jing W.
Sladek, Robert
Martinez-Sanchez, Aida
Rutter, Guy A.
Molecular phenotyping of single pancreatic islet leader beta cells by "Flash-Seq"
description Aims: Spatially-organized increases in cytosolic Ca2+ within pancreatic beta cells in the pancreatic islet underlie the stimulation of insulin secretion by high glucose. Recent data have revealed the existence of subpopulations of beta cells including “leaders” which initiate Ca2+ waves. Whether leader cells possess unique molecular features, or localisation, is unknown. Main methods: High speed confocal Ca2+ imaging was used to identify leader cells and connectivity analysis, running under MATLAB and Python, to identify highly connected “hub” cells. To explore transcriptomic differences between beta cell sub-groups, individual leaders or followers were labelled by photo-activation of the cryptic fluorescent protein PA-mCherry and subjected to single cell RNA sequencing (“Flash-Seq”). Key findings: Distinct Ca2+ wave types were identified in individual islets, with leader cells present in 73 % (28 of 38 islets imaged). Scale-free, power law-adherent behaviour was also observed in 29 % of islets, though “hub” cells in these islets did not overlap with leaders. Transcripts differentially expressed (295; padj < 0.05) between leader and follower cells included genes involved in cilium biogenesis and transcriptional regulation. Providing some support for these findings, ADCY6 immunoreactivity tended to be higher in leader than follower cells, whereas cilia number and length tended to be lower in the former. Finally, leader cells were located significantly closer to delta, but not alpha, cells in Euclidian space than were follower cells. Significance: The existence of both a discrete transcriptome and unique localisation implies a role for these features in defining the specialized function of leaders. These data also raise the possibility that localised signalling between delta and leader cells contributes to the initiation and propagation of islet Ca2+ waves.
author2 Lee Kong Chian School of Medicine (LKCMedicine)
author_facet Lee Kong Chian School of Medicine (LKCMedicine)
Chabosseau, Pauline
Yong, Fiona
Delgadillo-Silva, Luis F.
Lee, Eun Young
Melhem, Rana
Li, Shiying
Gandhi, Nidhi
Wastin, Jules
Noriega, Livia Lopez
Leclerc, Isabelle
Ali, Yusuf
Hughes, Jing W.
Sladek, Robert
Martinez-Sanchez, Aida
Rutter, Guy A.
format Article
author Chabosseau, Pauline
Yong, Fiona
Delgadillo-Silva, Luis F.
Lee, Eun Young
Melhem, Rana
Li, Shiying
Gandhi, Nidhi
Wastin, Jules
Noriega, Livia Lopez
Leclerc, Isabelle
Ali, Yusuf
Hughes, Jing W.
Sladek, Robert
Martinez-Sanchez, Aida
Rutter, Guy A.
author_sort Chabosseau, Pauline
title Molecular phenotyping of single pancreatic islet leader beta cells by "Flash-Seq"
title_short Molecular phenotyping of single pancreatic islet leader beta cells by "Flash-Seq"
title_full Molecular phenotyping of single pancreatic islet leader beta cells by "Flash-Seq"
title_fullStr Molecular phenotyping of single pancreatic islet leader beta cells by "Flash-Seq"
title_full_unstemmed Molecular phenotyping of single pancreatic islet leader beta cells by "Flash-Seq"
title_sort molecular phenotyping of single pancreatic islet leader beta cells by "flash-seq"
publishDate 2023
url https://hdl.handle.net/10356/171807
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