Loss of Uncoupling Protein 1 Expression in the Subcutaneous Adipose Tissue Predicts Childhood Obesity.
Katalin GyurinaMariia YarmakLászló Sasi-SzabóSarolta MolnárGábor MéhesTamás RöszerPublished in: International journal of molecular sciences (2023)
Stimulation of thermogenesis by inducing uncoupling protein 1 (UCP1) expression in adipocytes is thought to promote weight loss by increasing energy expenditure, and it is postulated that the human newborn has thermogenic subcutaneous fat depots. However, it remains unclear whether a relevant number of UCP1-expressing (UCP1 + ) adipocytes exist in the early postnatal life. Here we studied the distribution of UCP1 and the expression of thermogenic genes in the subcutaneous adipose tissues of the human fetus, infant and child. We show that the deep layer of human fetal and neonatal subcutaneous fat, particularly the abdominal wall, is rich in UCP1 + adipocytes. These adipocytes develop in the late third trimester and persist throughout childhood, expressing a panel of genes linked to mitochondrial biogenesis and thermogenesis. During the early childhood adiposity rebound-a critical phase that determines obesity risk later in life-the absence of adipose tissue UCP1 expression in children with normal body mass index (BMI) correlates with an obesity-associated gene expression signature. Finally, UCP1 expression is negatively correlated with BMI z -score and adipocyte size in infants and children. Overall, our results show that the absence of UCP1 expression in adipose tissue is an early indicator of adipose tissue expansion in children.
Keyphrases
- adipose tissue
- insulin resistance
- poor prognosis
- high fat diet
- body mass index
- weight loss
- gene expression
- endothelial cells
- weight gain
- binding protein
- young adults
- metabolic syndrome
- high fat diet induced
- bariatric surgery
- induced pluripotent stem cells
- oxidative stress
- long non coding rna
- pregnant women
- physical activity
- genome wide
- transcription factor
- small molecule
- obese patients
- preterm birth
- early life
- nitric oxide synthase