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:2022:10.1101/2022.08.26.505442,
author = {Chabosseau, P and Yong, F and Delgadillo-Silva, LF and Lee, EY 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 = {10.1101/2022.08.26.505442},
title = {Molecular phenotyping of single pancreatic islet leader beta cells by “Flash-Seq”},
url = {http://dx.doi.org/10.1101/2022.08.26.505442},
year = {2022}
}

RIS format (EndNote, RefMan)

TY  - JOUR
AB - <jats:title>Abstract</jats:title><jats:sec><jats:title>Aims</jats:title><jats:p>Spatially-organised increases in cytosolic Ca<jats:sup>2+</jats:sup>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 Ca<jats:sup>2+</jats:sup>waves. Whether leader cells possess unique molecular features, or localisation, is unknown.</jats:p></jats:sec><jats:sec><jats:title>Main methods</jats:title><jats:p>High speed confocal Ca<jats:sup>2+</jats:sup>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”).</jats:p></jats:sec><jats:sec><jats:title>Key findings</jats:title><jats:p>Distinct Ca<jats:sup>2+</jats:sup>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. Functionally validating these findings, cilia number and length tended to be lower in leader<jats:italic>vs</jats:italic>follower cells. Leader cells were also located significantly closer to delta cells in Euclidian space than were follower cells.</jats:p>
AU - Chabosseau,P
AU - Yong,F
AU - Delgadillo-Silva,LF
AU - Lee,EY
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 - 10.1101/2022.08.26.505442
PY - 2022///
TI - Molecular phenotyping of single pancreatic islet leader beta cells by “Flash-Seq”
UR - http://dx.doi.org/10.1101/2022.08.26.505442
ER -