| Title: |
Human alpha cell transcriptomic signatures of types 1 and 2 diabetes highlight disease-specific dysfunction pathways |
| Authors: |
Bosi, E; Marchetti, P; Rutter, GA; Eizirik, DL |
| Contributors: |
Medical Research Council; Wellcome Trust |
| Publisher Information: |
Cell Press |
| Publication Year: |
2022 |
| Collection: |
Imperial College London: Spiral |
| Subject Terms: |
Biological sciences; bioinformatics; transcriptomics |
| Subject Geographic: |
United States |
| Description: |
Although glucagon secretion is perturbed in both T1D and T2D, the pathophysiological changes in individual pancreatic alpha cells are still obscure. Using recently curated single-cell RNASeq data from T1D or T2D donors and their controls, we identified alpha cell transcriptomic alterations consistent with both common and discrete pathways. Although alterations in alpha cell identity gene (ARX, MAFB) expression were conserved, cytokine-regulated genes and genes involved in glucagon biosynthesis and processing were up-regulated in T1D. Conversely, mitochondrial genes associated with ROS (COX7B, NQO2) were dysregulated in T2D. Additionally, T1D alpha cells displayed altered expression of autoimmune-induced ER stress genes (ERLEC1, HSP90), whilst those from T2D subjects showed modified glycolytic and citrate cycle gene (LDHA?, PDHB, PDK4) expression. Thus, despite conserved alterations related to loss of function, alpha cells display disease-specific gene signatures which may be secondary to the main pathogenic events in each disease, namely immune- or metabolism-mediated-stress, in T1D and T2D, respectively. |
| Document Type: |
article in journal/newspaper |
| Language: |
English |
| Relation: |
iScience; http://hdl.handle.net/10044/1/99962; MR/R022259/1 (2018 – 2023); 212625/Z/18/Z |
| DOI: |
10.1016/j.isci.2022.105056 |
| Availability: |
http://hdl.handle.net/10044/1/99962; https://doi.org/10.1016/j.isci.2022.105056 |
| Rights: |
© 2022 The Authors. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/) ; http://creativecommons.org/licenses/by-nc-nd/4.0/ |
| Accession Number: |
edsbas.DE0D96A8 |
| Database: |
BASE |