Functional expression of glucose-dependent insulinotropic polypeptide receptors is coupled to differentiation in a human adipocyte model
Abstract
Objective To establish that human adipocytes express functional glucose-dependent insulinotropic peptide (GIP) receptors and in particular the regulation of GIP receptor (GIPR) expression in the context of the dynamic process of adipocyte differentiation. Design A combination of semiquantitative real-time PCR and measurement of GIP-stimulated cAMP accumulation was used to establish the expression and functional coupling of GIPRs during in vitro differentiation of human Simpson-Golabi-Behmel syndrome (SGBS) preadipocytes. Results Semiquantitative real-time PCR revealed that GIPR expression was substantially increased by day 4 of differentiation, reaching a maximum around 6-8 days (approximately 200-fold increase above undifferentiated cells, n=2). We also analysed the expression of the adipocyte fatty acid binding protein (FABP4) to relate GIPR expression to a molecular differentiation marker of adipogenesis. FABP4 expression was barely detectable in undifferentiated cells. However, following exposure to adipogenic medium, FABP4 expression gradually increased, with a maximal expression level around 10 days (approximately 1,600,000-fold increase above undifferentiated cells, n=2). Thus, the increases in GIPR mRNA during adipogenesis occur earlier than FABP4, suggesting that it might represent a gene expressed early in terminal differentiation and thus plays a role in fat droplet formation. A unit of 1 microM GIP failed to raise intracellular cAMP levels above basal levels in un…
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In human adipocytes, GIP receptors are present and functionally active.
“In human adipocytes, GIP receptors are present and functionally active [23‐25].”
From Tirzepatide as monotherapy improved markers of beta-cell function and insulin sensitivity in type 2 diabetes (SURPASS-1). (2023) · cites this paper as [25]
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Self-citationASSOCIATION BETWEEN GIP GENE POLYMORPHISM AND OBESE ADULTS IN BABYLON GOVERNORATE, IRAQ
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- Authors
- Weaver, R. E., Donnelly, D., Wabitsch, M., Grant, P. J., & Balmforth, A. J.
- Affiliations
- University of Leeds (GB)
- Universität Ulm (DE)
- Corresponding author
- Balmforth, A J
- Venue
- International Journal of Obesity
- Published
- 2008-09-09
- Volume
- 32
- Issue
- 11
- Pages
- 1705-1711
- ISSN
- 0307-0565 (ISSN-L)
- 1476-5497
- OpenAlex
- W1983641973
- Cited by
- 63
- References
- 39
- Citations by year
- 2026: 3 · 2025: 7 · 2024: 5 · 2023: 3 · 2022: 8 · 2021: 3 · 2020: 3 · 2019: 4 · 2018: 1 · 2016: 3 · 2015: 2 · 2014: 1 · 2013: 1 · 2012: 5
- FWCI
- 3.17
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- www.springer.com/tdm (tdm)
- Locations
- International Journal of Obesity (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Biotechnology and Biological Sciences Research Council
- Topics
- Health Sciences › Medicine › Physiology › Adipose Tissue and Metabolism
- Health Sciences › Medicine › Epidemiology › Adipokines, Inflammation, and Metabolic Diseases
- Health Sciences › Medicine › Surgery › Pancreatic function and diabetes
- Keywords
- glucose-dependent insulinotropic polypeptide, GIP receptor, adipogenesis, FABP4, cAMP accumulation, fat deposition
- MeSH terms
- Cell Differentiation, Cell Line, Cells, Cultured, Gastric Inhibitory Polypeptide, Humans, Receptors, Gastrointestinal Hormone, RNA, Messenger, Gene Expression, Adipocytes, Insulin-Secreting Cells
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