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Published on: June 30, 2017
Anti-inflammatory properties of bone morphogenetic protein 4 in human adipocytes
E Baraban1, T Chavakis1,2, B S Hamilton3
1Division of Molecular Endocrinology, Medical Clinic III, Technische Universität Dresden, Dresden, Germany.
Background:
Obesity is characterized by increased adipocyte number and size as well as white adipose tissue (WAT) inflammation, which is fundamental for the development of insulin resistance and type-2 diabetes. These processes, regulated by various endocrine, paracrine and autocrine factors, are extensively studied with the hope to interfere and to inhibit weight gain and related complications in obese patients. Recent data suggest an important role of bone morphogenic protein 4 (BMP4) in the regulation of adipogenesis and development of obesity. BMP4 is a growth factor of the transforming growth factor-β superfamily. Initially, BMPs were identified as inducers of ectopic bone formation. It is now apparent, however, that these proteins have different pleiotropic developmental actions and including playing a role in white adipogenesis.
Methods And Results:
Here, we demonstrate that the expression of BMP4 in human WAT is negatively correlated to body mass index and to the expression of pro-inflammatory cytokines. In vitro, BMP4 expression in cultured human adipocytes is upregulated after induction of differentiation. Cells treated with exogenous BMP4 increased peroxisome proliferator-activated receptor γ (PPARγ) expression and significantly reduced the expression of pro-inflammatory cytokines including tumor necrosis factor α (TNF-α) and monocyte chemoattractant protein 1. TNF-α treatment of fully differentiated adipocytes resulted in downregulation of the expression of adipogenic genes and elevated expression of pro-inflammatory cytokines. Exogenous BMP4 addition significantly reduced the negative effect of TNF-α on the expression profile of adipocytes. Finally, treatment of human adipocytes with exogenous BMP4 reduced the adipocytes' chemoattractant potential and the migration of monocytes toward adipocyte-conditioned medium.
Conclusions:
These results indicate that BMP4 is an important anti-inflammatory molecule, which may act through PPARγ and reduces TNF-α-mediated pro-inflammatory cytokine production in human adipocytes. Through its anti-inflammatory potential, BMP4 may serve as a protective factor for inflammation-related diseases such as insulin-tolerance or type-2 diabetes.
Insights
Bone morphogenic protein 4 (BMP4) acts as an anti-inflammatory agent in human white adipose tissue, reducing inflammatory markers and protecting against obesity-related diseases like type-2 diabetes.
Area of Science:
- Endocrinology and Metabolism
- Molecular Biology
- Adipose Tissue Biology
Background:
- Obesity is linked to white adipose tissue (WAT) inflammation, contributing to insulin resistance and type-2 diabetes.
- Bone morphogenic protein 4 (BMP4) is implicated in adipogenesis and obesity development.
- BMP4 is a growth factor within the transforming growth factor-β superfamily with diverse developmental roles.
Purpose of the Study:
- To investigate the role of BMP4 in human white adipose tissue.
- To determine BMP4's effect on adipocyte inflammation and differentiation.
- To explore BMP4's potential as a therapeutic target for obesity-related complications.
Main Methods:
- Correlation analysis of BMP4 expression with BMI and inflammatory markers in human WAT.
- In vitro studies using cultured human adipocytes treated with BMP4 and tumor necrosis factor α (TNF-α).
- Assessment of gene expression, adipogenic markers, and monocyte chemoattractant potential.
Main Results:
- BMP4 expression in human WAT negatively correlates with BMI and pro-inflammatory cytokines.
- Exogenous BMP4 upregulates peroxisome proliferator-activated receptor γ (PPARγ) and reduces pro-inflammatory cytokines (TNF-α, MCP-1) in adipocytes.
- BMP4 mitigates TNF-α-induced negative effects on adipocytes and reduces monocyte migration.
Conclusions:
- BMP4 exhibits significant anti-inflammatory properties in human adipocytes, potentially via PPARγ.
- BMP4 reduces TNF-α-mediated inflammation and adipocyte chemoattractant potential.
- BMP4 may serve as a protective factor against inflammation-related diseases like insulin resistance and type-2 diabetes.
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