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Published in: Diabetologia 8/2022

Open Access 28-04-2022 | Type 2 Diabetes | Review

Lessons from single-cell RNA sequencing of human islets

Authors: Mtakai Ngara, Nils Wierup

Published in: Diabetologia | Issue 8/2022

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Abstract

Islet dysfunction is central in type 2 diabetes and full-blown type 2 diabetes develops first when the beta cells lose their ability to secrete adequate amounts of insulin in response to raised plasma glucose. Several mechanisms behind beta cell dysfunction have been put forward but many important questions still remain. Furthermore, our understanding of the contribution of each islet cell type in type 2 diabetes pathophysiology has been limited by technical boundaries. Closing this knowledge gap will lead to a leap forward in our understanding of the islet as an organ and potentially lead to improved treatments. The development of single-cell RNA sequencing (scRNAseq) has led to a breakthrough for characterising the transcriptome of each islet cell type and several important observations on the regulation of cell-type-specific gene expression have been made. When it comes to identifying type 2 diabetes disease mechanisms, the outcome is still limited. Several studies have identified differentially expressed genes, although there is very limited consensus between the studies. As with all new techniques, scRNAseq has limitations; in addition to being extremely expensive, genes expressed at low levels may not be detected, noise may not be appropriately filtered and selection biases for certain cell types are at hand. Furthermore, recent advances suggest that commonly used computational tools may be suboptimal for analysis of scRNAseq data in small-scale studies. Fortunately, development of new computational tools holds promise for harnessing the full potential of scRNAseq data. Here we summarise how scRNAseq has contributed to increasing the understanding of various aspects of islet biology as well as type 2 diabetes disease mechanisms. We also focus on challenges that remain and propose steps to promote the utilisation of the full potential of scRNAseq in this area.

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Appendix
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Literature
68.
go back to reference Alumets J, Hakanson R, Sundler F (1983) Ontogeny of endocrine cells in porcine gut and pancreas. An immunocytochemical study. Gastroenterology 85(6):1359–1372CrossRef Alumets J, Hakanson R, Sundler F (1983) Ontogeny of endocrine cells in porcine gut and pancreas. An immunocytochemical study. Gastroenterology 85(6):1359–1372CrossRef
Metadata
Title
Lessons from single-cell RNA sequencing of human islets
Authors
Mtakai Ngara
Nils Wierup
Publication date
28-04-2022
Publisher
Springer Berlin Heidelberg
Keyword
Type 2 Diabetes
Published in
Diabetologia / Issue 8/2022
Print ISSN: 0012-186X
Electronic ISSN: 1432-0428
DOI
https://doi.org/10.1007/s00125-022-05699-1

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