Phosphoproteomics Reveals the GSK3-PDX1 Axis as a Key Pathogenic Signaling Node in Diabetic Islets

Research output: Contribution to journal › Journal article › Research › peer-review

Standard

Phosphoproteomics Reveals the GSK3-PDX1 Axis as a Key Pathogenic Signaling Node in Diabetic Islets. / Sacco, Francesca; Seelig, Anett; Humphrey, Sean J; Krahmer, Natalie; Volta, Francesco; Reggio, Alessio; Marchetti, Piero; Gerdes, Jantje; Mann, Matthias.

In: Cell Metabolism, 07.03.2019.

Research output: Contribution to journal › Journal article › Research › peer-review

Harvard

Sacco, F, Seelig, A, Humphrey, SJ, Krahmer, N, Volta, F, Reggio, A, Marchetti, P, Gerdes, J & Mann, M 2019, 'Phosphoproteomics Reveals the GSK3-PDX1 Axis as a Key Pathogenic Signaling Node in Diabetic Islets', Cell Metabolism. https://doi.org/10.1016/j.cmet.2019.02.012

APA

Sacco, F., Seelig, A., Humphrey, S. J., Krahmer, N., Volta, F., Reggio, A., Marchetti, P., Gerdes, J., & Mann, M. (2019). Phosphoproteomics Reveals the GSK3-PDX1 Axis as a Key Pathogenic Signaling Node in Diabetic Islets. Cell Metabolism. https://doi.org/10.1016/j.cmet.2019.02.012

Vancouver

Sacco F, Seelig A, Humphrey SJ, Krahmer N, Volta F, Reggio A et al. Phosphoproteomics Reveals the GSK3-PDX1 Axis as a Key Pathogenic Signaling Node in Diabetic Islets. Cell Metabolism. 2019 Mar 7. https://doi.org/10.1016/j.cmet.2019.02.012

Author

Sacco, Francesca ; Seelig, Anett ; Humphrey, Sean J ; Krahmer, Natalie ; Volta, Francesco ; Reggio, Alessio ; Marchetti, Piero ; Gerdes, Jantje ; Mann, Matthias. / Phosphoproteomics Reveals the GSK3-PDX1 Axis as a Key Pathogenic Signaling Node in Diabetic Islets. In: Cell Metabolism. 2019.

Bibtex

@article{952dde372acf486696b5c1455a968352,
title = "Phosphoproteomics Reveals the GSK3-PDX1 Axis as a Key Pathogenic Signaling Node in Diabetic Islets",
abstract = "Progressive decline of pancreatic beta cell function is central to the pathogenesis of type 2 diabetes. Protein phosphorylation regulates glucose-stimulated insulin secretion from beta cells, but how signaling networks are remodeled in diabetic islets in vivo remains unknown. Using high-sensitivity mass spectrometry-based proteomics, we quantified 6,500 proteins and 13,000 phosphopeptides in islets of obese diabetic mice and matched controls, revealing drastic remodeling of key kinase hubs and signaling pathways. Integration with a literature-derived signaling network implicated GSK3 kinase in the control of the beta cell-specific transcription factor PDX1. Deep phosphoproteomic analysis of human islets chronically treated with high glucose demonstrated a conserved glucotoxicity-dependent role of GSK3 kinase in regulating insulin secretion. Remarkably, the ability of beta cells to secrete insulin in response to glucose was rescued almost completely by pharmacological inhibition of GSK3. Thus, our resource enables investigation of mechanisms and drug targets in type 2 diabetes.",
author = "Francesca Sacco and Anett Seelig and Humphrey, {Sean J} and Natalie Krahmer and Francesco Volta and Alessio Reggio and Piero Marchetti and Jantje Gerdes and Matthias Mann",
note = "Copyright {\textcopyright} 2019 Elsevier Inc. All rights reserved.",
year = "2019",
month = mar,
day = "7",
doi = "10.1016/j.cmet.2019.02.012",
language = "English",
journal = "Cell Metabolism",
issn = "1550-4131",
publisher = "Cell Press",

}

RIS

TY - JOUR

T1 - Phosphoproteomics Reveals the GSK3-PDX1 Axis as a Key Pathogenic Signaling Node in Diabetic Islets

AU - Sacco, Francesca

AU - Seelig, Anett

AU - Humphrey, Sean J

AU - Krahmer, Natalie

AU - Volta, Francesco

AU - Reggio, Alessio

AU - Marchetti, Piero

AU - Gerdes, Jantje

AU - Mann, Matthias

N1 - Copyright © 2019 Elsevier Inc. All rights reserved.

PY - 2019/3/7

Y1 - 2019/3/7

N2 - Progressive decline of pancreatic beta cell function is central to the pathogenesis of type 2 diabetes. Protein phosphorylation regulates glucose-stimulated insulin secretion from beta cells, but how signaling networks are remodeled in diabetic islets in vivo remains unknown. Using high-sensitivity mass spectrometry-based proteomics, we quantified 6,500 proteins and 13,000 phosphopeptides in islets of obese diabetic mice and matched controls, revealing drastic remodeling of key kinase hubs and signaling pathways. Integration with a literature-derived signaling network implicated GSK3 kinase in the control of the beta cell-specific transcription factor PDX1. Deep phosphoproteomic analysis of human islets chronically treated with high glucose demonstrated a conserved glucotoxicity-dependent role of GSK3 kinase in regulating insulin secretion. Remarkably, the ability of beta cells to secrete insulin in response to glucose was rescued almost completely by pharmacological inhibition of GSK3. Thus, our resource enables investigation of mechanisms and drug targets in type 2 diabetes.

AB - Progressive decline of pancreatic beta cell function is central to the pathogenesis of type 2 diabetes. Protein phosphorylation regulates glucose-stimulated insulin secretion from beta cells, but how signaling networks are remodeled in diabetic islets in vivo remains unknown. Using high-sensitivity mass spectrometry-based proteomics, we quantified 6,500 proteins and 13,000 phosphopeptides in islets of obese diabetic mice and matched controls, revealing drastic remodeling of key kinase hubs and signaling pathways. Integration with a literature-derived signaling network implicated GSK3 kinase in the control of the beta cell-specific transcription factor PDX1. Deep phosphoproteomic analysis of human islets chronically treated with high glucose demonstrated a conserved glucotoxicity-dependent role of GSK3 kinase in regulating insulin secretion. Remarkably, the ability of beta cells to secrete insulin in response to glucose was rescued almost completely by pharmacological inhibition of GSK3. Thus, our resource enables investigation of mechanisms and drug targets in type 2 diabetes.

U2 - 10.1016/j.cmet.2019.02.012

DO - 10.1016/j.cmet.2019.02.012

M3 - Journal article

C2 - 30879985

JO - Cell Metabolism

JF - Cell Metabolism

SN - 1550-4131

ER -

ID: 216015461