PDE4D and PDE3B orchestrate distinct cAMP microdomains in 3T3‐L1 adipocytes

The discovery of LD-associated cAMP as a distinct subcellular pool suggests that cAMP signalling in adipocytes is more compartmentalized than previously recognized. The distinct pathways by which FGF1 and insulin regulate adipose cell cAMP levels highlight that antilipolytic signalling is not uniform, refining our understanding of lipolysis regulation.

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Publication Details

Journal
British Journal of Pharmacology
Published
2025-10-13
DOI
https://doi.org/10.1111/bph.70216
Primary Topic
Pancreatic function and diabetes
Type
article
Field-Weighted Citation Impact
0.00

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article

PDE4D and PDE3B orchestrate distinct cAMP microdomains in 3T3‐L1 adipocytes

Andreas L. Birkenfeld, Lisa Jacob, Robert Łukowski, Johannes Krier et al.
British Journal of Pharmacology
Pancreatic function and diabetes
article

PDE4D and PDE3B orchestrate distinct cAMP microdomains in 3T3‐L1 adipocytes

Andreas L. Birkenfeld, Lisa Jacob, Robert Łukowski, Johannes Krier, Gencer Sancar, Siegfried Ussar, Judith Seigner, David Arturo Juarez Lopez, D. R. Spahn, Judith Leonie Nono
article en

Abstract

The discovery of LD-associated cAMP as a distinct subcellular pool suggests that cAMP signalling in adipocytes is more compartmentalized than previously recognized. The distinct pathways by which FGF1 and insulin regulate adipose cell cAMP levels highlight that antilipolytic signalling is not uniform, refining our understanding of lipolysis regulation.

British Journal of Pharmacology
Helmholtz Zentrum München (DE), Deutsches Diabetes-Zentrum e.V. (DE), German Center for Diabetes Research (DE), Heinrich Heine University Düsseldorf (DE), University of Tübingen (DE)
Deutsche Forschungsgemeinschaft
Openalex Percentile: Top 55%
Pancreatic function and diabetes
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PDE4D and PDE3B orchestrate distinct cAMP microdomains in 3T3‐L1 adipocytes — Andreas L. Birkenfeld, Lisa Jacob, et al. · British Journal of Pharmacology (2025) | TGRS Research Map | TGRS