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Published on: June 3, 2016
Adipocyte C1QTNF5 expression is BMI-dependently related to early adipose tissue dysfunction and systemic CTRP5 serum
J T Schwartze1, K Landgraf1,2, U Spielau2
1Department of Women's and Child Health, Center for Pediatric Research Leipzig (CPL), University Hospital for Children &Adolescents, University of Leipzig, Leipzig, Germany.
Insights
Adipocyte C1QTNF5 expression in children increases with obesity and correlates with metabolic dysfunction. This adipocytokine is linked to adipose tissue alterations and is regulated by TNFα, suggesting a role in childhood obesity-related metabolic issues.
Area of Science:
- Endocrinology
- Metabolic Research
- Adipose Tissue Biology
Background:
- C1QTNF5 (CTRP5) inhibits insulin signaling in adipocytes.
- Its role in childhood obesity and metabolic dysfunction is unknown.
Purpose of the Study:
- To investigate the correlation between adipocyte C1QTNF5 expression and obesity in children.
- To examine associations with systemic CTRP5 levels and adipose tissue (AT) alterations.
Main Methods:
- Quantitative real-time PCR and ELISA were used to assess C1QTNF5 expression in subcutaneous AT and serum.
- Samples were collected from lean and overweight/obese children.
Main Results:
- Adipocyte C1QTNF5 expression positively correlated with BMI SDS, body fat percentage, and adipocyte number.
- Expression was linked to obesity-related AT alterations (e.g., crown-like structures) and metabolic markers (insulin, leptin).
- Tumor necrosis factor-alpha (TNFα) induced C1QTNF5 in adipocytes in vitro.
Conclusions:
- Adipocyte C1QTNF5 expression is strongly associated with obesity degree in children.
- It correlates with AT alterations, systemic CTRP5 levels, and metabolic disease markers.
- TNFα positively regulates C1QTNF5 expression in adipocytes.
Background/Objectives:
The recently identified adipocytokine C1QTNF5 (encodes for CTRP5) has been demonstrated to inhibit pro-metabolic insulin signaling in adipocytes. We hypothesized that adipocyte C1QTNF5 expression in subcutaneous (sc) adipose tissue (AT) would correlate with the degree of obesity, systemic CTRP5 serum levels, and early AT and metabolic dysfunction in children.
Subjects/Methods:
Sc AT samples were obtained from 33 healthy Caucasian lean children aged 10.06±4.84 years and 42 overweight and obese children aged 13.34±3.12 years. C1QTNF5 expression in sc AT as well as in investigated cell lines was assessed by quantitative real-time PCR. Systemic CTRP5 levels were assessed by ELISA.
Results:
C1QTNF5 expression in sc adipocytes increased with body mass index (BMI) standard deviation score (SDS; R=0.48, P<0.001), body fat percentage (R=0.4, P=0.004), adipocyte number (R=0.69, P<0.001) and systemic CTRP5 serum levels (R=0.28, P=0.025) whereas expression in the stromal vascular fraction (SVF) was inversely correlated with BMI SDS (R=-0.24, P=0.04). Multiple regression analysis confirmed that BMI SDS was the strongest independent predictor for C1QTNF5 expression in sc adipocytes. SVF C1QTNF5 levels strongly correlated with SVF CD31 expression (R=0.54, P<0.001) indicating expression by endothelial cells. Primary human endothelial cells demonstrated stronger expression compared with human Simpson-Golahbi-Behmel syndrome pre-adipocytes and adipocytes. Adipocyte C1QTNF5 expression levels were BMI-dependently related to fasting insulin (R=0.3, P=0.03) and leptin serum levels (R=0.5, P<0.001). Sc AT samples containing crown-like structures (CLS) demonstrated increased adipocyte C1QTNF5 expression compared to CLS-negative samples (P=0.03). Functionally, tumor necrosis factor (TNF)α caused a fourfold induction of C1QTNF5 in human adipocytes (P<0.001) and a 50% reduction in primary human endothelial cells (P<0.001).
Conclusions:
In children adipocyte C1QTNF5 expression is already strongly related to the degree of obesity and is associated with obesity-related AT alterations, systemic CTRP5 serum levels as well as circulating markers of metabolic disease and is positively regulated by TNFα in vitro.
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