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Updated: Apr 16, 2026

Mechanism of Regulation of Adipocyte Numbers in Adult Organisms Through Differentiation and Apoptosis Homeostasis
Published on: June 3, 2016
Biphasic effects of FGF2 on adipogenesis
Sooho Kim1, Chihoon Ahn2, Naeun Bong1
1Laboratory of Genome to Drug Medicine, joint Center for Biosciences, Incheon, Korea.
Fibroblast Growth Factor 2 (FGF2) has a dual role in fat cell development (adipogenesis). Low concentrations promote it, while high concentrations inhibit it by affecting the ERK pathway.
Area of Science:
- Biochemistry
- Cell Biology
- Stem Cell Research
Background:
- Conflicting reports exist on Fibroblast Growth Factor 2's (FGF2) role in adipogenesis.
- Previous studies on FGF2's effect on adipogenesis in vitro have yielded inconsistent results.
Purpose of the Study:
- To investigate the concentration-dependent effects of FGF2 on in vitro adipogenesis.
- To elucidate the molecular mechanisms underlying FGF2's influence on adipogenesis and adipose tissue development.
Main Methods:
- Utilized human adipose-derived stem cells (hASCs) for in vitro culture.
- Investigated the role of FGF2 at varying concentrations (low < 2 ng/ml, high > 10 ng/ml).
- Analyzed the activation of the ERK signaling pathway and its regulation by FGF2.
Main Results:
- FGF2 at low concentrations (< 2 ng/ml) enhanced hASC adipogenesis.
- FGF2 at high concentrations (> 10 ng/ml) suppressed adipogenesis by sustaining ERK phosphorylation.
- High FGF2 concentrations acted as a dominant negative factor against BMP ligands.
- Lower FGF2 expression was observed in fat tissues of obese mice compared to normal mice.
Conclusions:
- FGF2 exhibits a concentration-dependent biphasic effect on adipogenesis.
- FGF2's dominant-negative effect on BMP ligands contributes to its inhibitory role.
- Findings provide a mechanistic understanding of FGF2's role in adipogenesis and fat tissue regulation.
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