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Published on: February 17, 2021
Using neonatal skin to study the developmental programming of aging
Leryn J Reynolds1, Brett J Dickens1, Benjamin B Green2
1Department of Pharmacology and Nutritional Sciences, University of Kentucky, Lexington, KY 40536, USA.
Insights
Human neonatal foreskin offers a new way to study how early-life exposures impact obesity and diabetes risk. This research shows foreskin cells can model key processes like fat development and insulin response.
Area of Science:
- Developmental biology
- Metabolic disease research
- Human neonate studies
Background:
- Maternal exposures during pregnancy can influence offspring's risk for chronic diseases.
- Obesity and type 2 diabetes are significant age-associated diseases.
- Understanding developmental programming is crucial for preventing these conditions.
Purpose of the Study:
- To introduce human neonatal foreskin as a novel model for studying developmental programming.
- To investigate adipogenesis and insulin receptor signaling in neonatal foreskin.
- To link neonatal development to long-term risks of obesity and diabetes.
Main Methods:
- Collected neonatal foreskin tissue post-circumcision.
- Isolated primary dermal fibroblasts from the foreskin.
- Performed in vitro adipocyte differentiation and insulin stimulation assays.
Main Results:
- Human neonatal foreskin fibroblasts successfully undergo lipid uptake when stimulated for differentiation.
- Foreskin fibroblasts exhibit functional insulin receptor signaling upon insulin stimulation.
- These findings validate the foreskin model for studying metabolic processes.
Conclusions:
- Neonatal foreskin is a viable and novel human model for studying developmental programming.
- This model can be used to investigate the impact of early-life exposures on adipogenesis and insulin signaling.
- Foreskin research may provide insights into preventing neonatal obesity and diabetes.
Abstract:
Numerous studies have examined how both negative and positive maternal exposures (environmental contaminants, nutrition, exercise, etc.) impact offspring risk for age-associated diseases such as obesity, type 2 diabetes, hypertension, and others. The purpose of this study was to introduce the foreskin as a novel model to examine developmental programming in human neonates, particularly in regard to adipogenesis and insulin receptor signaling, major contributors to age-associated diseases such as obesity and diabetes. Neonatal foreskin was collected following circumcision and primary dermal fibroblasts were isolated to perform adipocyte differentiation and insulin stimulation experiments. Human neonatal foreskin primary fibroblasts take up lipid when stimulated with a differentiation cocktail and demonstrate insulin signaling when stimulated with insulin. Thus, we propose that foreskin tissue can be used to study developmental exposures and programming that occur in the neonate as it relates to age-associated diseases such as obesity and diabetes.
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