Adipose Tissue: A Metabolic Regulator. Potential Implications for the Metabolic Outcome of Subjects Born Small for Gestational Age (SGA)
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Updated: Jul 9, 2026

Mechanism of Regulation of Adipocyte Numbers in Adult Organisms Through Differentiation and Apoptosis Homeostasis
Published on: June 3, 2016
Arianna Maiorana1, Chiara Del Bianco, Stefano Cianfarani
1Rina Balducci Center of Pediatric Endocrinology, Department of Public Health and Cell Biology, Tor Vergata University, 00133-Rome, Italy.
Insights
Understanding visceral adipose tissue stem cells is crucial for metabolic health. Research suggests their behavior may explain long-term risks associated with low birth weight and intrauterine growth retardation.
Area of Science:
- Metabolic regulation and stem cell biology.
Background:
- Adipose tissue regulates metabolism, energy, and immunity.
- Abdominal obesity contributes to insulin resistance via visceral adipose tissue (VAT) lipolysis and adipocytokine secretion.
- Low birth weight is linked to central adiposity and increased risk of metabolic syndrome, type 2 diabetes, and cardiovascular disease.
Purpose of the Study:
- To investigate the role of intrauterine adipogenesis in metabolic syndrome development.
- To understand the behavior of visceral adipose tissue-derived stem cells (VATSCS).
- To explore the clinical implications of VATSCS for intrauterine growth retardation (IUGR).
Main Methods:
- The study focuses on the behavior of VATSCS.
Main Results:
- VATSCS behavior is key to understanding metabolic risks in IUGR.
- Further research into VATSCS could reveal mechanisms linking fetal development to adult metabolic disease.
Conclusions:
- Studying VATSCS offers insights into metabolic alterations associated with IUGR.
- This knowledge has potential clinical applications for preventing long-term metabolic dysfunction.
Abstract:
Adipose tissue is involved in the regulation of glucose and lipid metabolism, energy balance, inflammation and immune response. Abdominal obesity plays a key role in the development of insulin resistance because of the high lipolytic rate of visceral adipose tissue and its secretion of adipocytokines. Low birth weight subjects are prone to central redistribution of adipose tissue and are at high risk of developing metabolic syndrome, type 2 diabetes and cardiovascular disease. Intrauterine adipogenesis may play a key role in the fetal origin of the pathogenesis of metabolic syndrome, type 2 diabetes and cardiovascular disease. Therefore, knowledge of the behavior of visceral adipose tissue-derived stem cells could provide a greater understanding of the metabolic risk related to intrauterine growth retardation, with potential clinical implications for the prevention of long-term metabolic alterations.
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