Cab45G trafficking through the insulin secretory pathway is altered in human type 2 diabetes

In type 2 diabetes (T2D), the rate of insulin secretory granule biogenesis can limit insulin secretion from pancreatic β-cells. Using rat insulinoma INS1 β-cells, we show that the soluble Ca<sup>2+</sup>-binding/trafficking protein, Cab45G, serves as a non-essential chaperone for insulin granule biogenesis. In β-cells, Cab45G is stored within a <i>cis</i>-Golgi reservoir. Cab45G deletion dysregulates Ca<sup>2+</sup> homeostasis and leads to secretory abnormality, but insulin granule biogenesis remains intact. Increasing Cab45G biosynthesis leads to anterograde trafficking into insulin granules, stimulating their production. Using human donor islets, we identify increased anterograde Cab45G trafficking in obese humans with and without T2D, consistent with the heightened demand for granule biogenesis. However, humans with T2D demonstrate decreased Golgi Cab45G localization and increased granule Cab45G localization compared to those without T2D. Our study provides the first insight into Cab45G function in specialized secretory cells and opens avenues of investigation into mechanisms associated with β-cell compensation and failure.

Authors

Institutions

Publication Details

Journal
iScience
Published
2024-12-30
DOI
https://doi.org/10.1016/j.isci.2024.111719
Primary Topic
Pancreatic function and diabetes
Type
article
Field-Weighted Citation Impact
0.00

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Cab45G trafficking through the insulin secretory pathway is altered in human type 2 diabetes

Matthew Taper, Jason Tong, Alexis Díaz‐Vegas, Jérôme Cattin‐Ortolá et al.
iScience
Pancreatic function and diabetes
article

Cab45G trafficking through the insulin secretory pathway is altered in human type 2 diabetes

Matthew Taper, Jason Tong, Alexis Díaz‐Vegas, Jérôme Cattin‐Ortolá, Helen E. Thomas, Elise J. Needham, Mark Larance, Melkam A. Kebede, Belinda Yau, A. Gabrielle J. van der Kraan, Sheyda Naghiloo, Mark Germanos, Peter Thorn, Amy L. Wilson, Kitty Sun, Cédric S. Asensio, Yousun An, Michael Ailion, Howard W. Blume, Thomas Loudovaris, Cara Yeoman, Drew Masler
article en

Abstract

In type 2 diabetes (T2D), the rate of insulin secretory granule biogenesis can limit insulin secretion from pancreatic β-cells. Using rat insulinoma INS1 β-cells, we show that the soluble Ca<sup>2+</sup>-binding/trafficking protein, Cab45G, serves as a non-essential chaperone for insulin granule biogenesis. In β-cells, Cab45G is stored within a <i>cis</i>-Golgi reservoir. Cab45G deletion dysregulates Ca<sup>2+</sup> homeostasis and leads to secretory abnormality, but insulin granule biogenesis remains intact. Increasing Cab45G biosynthesis leads to anterograde trafficking into insulin granules, stimulating their production. Using human donor islets, we identify increased anterograde Cab45G trafficking in obese humans with and without T2D, consistent with the heightened demand for granule biogenesis. However, humans with T2D demonstrate decreased Golgi Cab45G localization and increased granule Cab45G localization compared to those without T2D. Our study provides the first insight into Cab45G function in specialized secretory cells and opens avenues of investigation into mechanisms associated with β-cell compensation and failure.

iScienceVol. 28(2)
The University of Sydney (AU), University of Denver (US), University of Washington (US), Yale University (US)
University of Sydney, National Institutes of Health, Medical Research Council, National Health and Medical Research Council
Gender equality
Openalex Percentile: Top 55%
Pancreatic function and diabetes
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.