Imperial College London

ProfessorGuyRutter

Faculty of MedicineDepartment of Medicine

Visiting Professor
 
 
 
//

Contact

 

+44 (0)20 7594 3340g.rutter Website

 
 
//

Location

 

ICTEM buildingHammersmith Campus

//

Summary

 

Publications

Citation

BibTex format

@article{Chabosseau:2023:10.1016/j.lfs.2023.121436,
author = {Chabosseau, P and Yong, F and Delgadillo-Silva, LF and Lee, EY and Melhem, R and Li, S and Gandhi, N and Wastin, J and Noriega, LL and Leclerc, I and Ali, Y and Hughes, JW and Sladek, R and Martinez-Sanchez, A and Rutter, GA},
doi = {10.1016/j.lfs.2023.121436},
journal = {Life Sciences},
title = {Molecular phenotyping of single pancreatic islet leader beta cells by "Flash-Seq"},
url = {http://dx.doi.org/10.1016/j.lfs.2023.121436},
volume = {316},
year = {2023}
}

RIS format (EndNote, RefMan)

TY  - JOUR
AB - 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.
AU - Chabosseau,P
AU - Yong,F
AU - Delgadillo-Silva,LF
AU - Lee,EY
AU - Melhem,R
AU - Li,S
AU - Gandhi,N
AU - Wastin,J
AU - Noriega,LL
AU - Leclerc,I
AU - Ali,Y
AU - Hughes,JW
AU - Sladek,R
AU - Martinez-Sanchez,A
AU - Rutter,GA
DO - 10.1016/j.lfs.2023.121436
PY - 2023///
SN - 0024-3205
TI - Molecular phenotyping of single pancreatic islet leader beta cells by "Flash-Seq"
T2 - Life Sciences
UR - http://dx.doi.org/10.1016/j.lfs.2023.121436
UR - https://www.ncbi.nlm.nih.gov/pubmed/36706832
UR - http://hdl.handle.net/10044/1/103018
VL - 316
ER -