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Updated: Feb 26, 2026

Mechanism of Regulation of Adipocyte Numbers in Adult Organisms Through Differentiation and Apoptosis Homeostasis
Published on: June 3, 2016
Adamts1 responds to systemic cues and gates adipogenesis
Janica C Wong1, Brian J Feldman1,2
1a Department of Pediatrics/Endocrinology , Stanford University School of Medicine , Stanford , CA , USA.
Excess calories expand fat tissue via adipocyte precursor cell (APC) differentiation. Our study identifies Adamts1 as a key regulator in this diet-responsive process, crucial for understanding fat tissue growth.
Area of Science:
- Metabolism and Endocrinology
- Cell Biology
- Molecular Biology
Background:
- Excess caloric intake leads to adipose tissue expansion.
- Adipose tissue expansion occurs via adipocyte hypertrophy and new adipocyte generation from adipocyte precursor cells (APCs).
- The precise signals controlling APC differentiation (adipogenesis) in response to diet are not fully understood.
Purpose of the Study:
- To identify novel regulators of adipogenesis.
- To investigate the role of Adamts1 in diet-induced adipose tissue expansion.
- To monitor endogenous APC activity in vivo during high-fat diet exposure.
Main Methods:
- Ex vivo studies of adipogenesis.
- Identification of Adamts1 as a glucocorticoid and diet-responsive factor.
- Application of sensitive tools for monitoring endogenous APC activity in vivo.
Main Results:
- Adamts1 acts as a regulator of an extracellular relay system.
- This system modulates the initiation of the intracellular adipogenesis program in APCs.
- Early in vivo response to high-fat diet in APCs was successfully monitored.
Conclusions:
- Adamts1 is a key signaling molecule linking systemic cues (diet, glucocorticoids) to local APC differentiation.
- Understanding Adamts1's role provides insights into adipose tissue expansion mechanisms.
- Novel tools enable real-time monitoring of APCs, facilitating further research into metabolic diseases.
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