AKT signaling in hepatocytes rapidly increases glucose phosphorylation and contribution to glycogen without affecting metabolite pool sizes or glycogen breakdown

Together, these results demonstrate that AKT acutely regulates glucose contribution to glycogen and its upstream precursors, suggesting a transcription-independent, glucokinase-centered mechanism for glycogen synthesis through the direct pathway.

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Publication Details

Journal
bioRxiv (Cold Spring Harbor Laboratory)
Published
2025-12-03
DOI
https://doi.org/10.64898/2025.12.01.691331
Primary Topic
Glycogen Storage Diseases and Myoclonus
Type
article
Field-Weighted Citation Impact
0.00
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article

AKT signaling in hepatocytes rapidly increases glucose phosphorylation and contribution to glycogen without affecting metabolite pool sizes or glycogen breakdown

Joseph A. Baur, Paul M. Titchenell, Joshua D. Rabinowitz, Megan Stefkovich et al.
bioRxiv (Cold Spring Harbor Laboratory)
Glycogen Storage Diseases and Myoclonus
article

AKT signaling in hepatocytes rapidly increases glucose phosphorylation and contribution to glycogen without affecting metabolite pool sizes or glycogen breakdown

Joseph A. Baur, Paul M. Titchenell, Joshua D. Rabinowitz, Megan Stefkovich, Won Dong Lee, Talia Coopersmith
article en

Abstract

Together, these results demonstrate that AKT acutely regulates glucose contribution to glycogen and its upstream precursors, suggesting a transcription-independent, glucokinase-centered mechanism for glycogen synthesis through the direct pathway.

bioRxiv (Cold Spring Harbor Laboratory)
Yonsei University (KR), Ludwig Cancer Research (BE), Princeton University (US), University of the Arts (US), Penn Center for AIDS Research (US), Ludwig Cancer Research (US), University of Pennsylvania (US)
Openalex Percentile: Top 45%
Glycogen Storage Diseases and Myoclonus
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