LLTH induces white adipose tissue browning via NF κB inhibition in ATM

This study aimed to explore the role of macrophage polarization and TLR4/NF-κB pathway in promoting browning of white adipose tissue through different hypoxic exercises. (1) Fifty obese female rats were selected after 16 weeks of high-fat diet feeding and randomly divided into normoxic sedentary (NC), normoxic exercise (NE), hypoxic sedentary (HC), Living-High Training-High (HH), and Living-Low Training-High (LH) groups. Four weeks of hypoxic and exercise interventions were conducted to investigate changes in the expression of the TLR4/NF-κB pathway and inflammatory factors in obese rat adipose tissue and the expression of genes and proteins related to adipose tissue browning. (2) After the 4-week intervention, adipose tissue macrophages (ATM) were isolated from HH and LH groups, activated with NF-κB activator, and co-cultured with adipocyte-induced adipose-derived stem cells to explore the role of the TLR4/NF-κB pathway in promoting browning of white adipose tissue by inducing changes in macrophage polarization through different hypoxic exercise. (1) After 4 weeks of different hypoxic interventions, the proportion of M1 macrophages decreased (p < 0.01), and HH intervention increased the proportion of M2 macrophages (p < 0.05). The protein expression levels of TLR4, NF-κB, p-NF-κB, and MyD88 in ATM of the HH and LH groups were significantly lower than those of the NC group (p < 0.01). Four weeks of LH intervention significantly upregulated the protein expression levels of CIDEA, C/EBP-β, PPAR-γ, PGC-1α, PRDM-16, and UCP-1 in rat adipose tissue (p < 0.01). (2) NF-κB activator intervention for 24 h significantly upregulated the protein expression levels of TLR4, p-NF-κB, and MyD88 in adipose tissue of HH and LH group rats (p < 0.01). NF-κB activator intervention for 24 h downregulated the protein expression levels of CIDEA, C/EBP-β, PPAR-γ, PGC-1α, PRDM-16, and UCP-1 in co-cultured adipocytes for 48 h in ATM of the LH group rats (p < 0.05). Four weeks of HH and LH interventions could reduce M1 polarization of ATM, downregulate the expression levels of the TLR4-NF-κB pathway in ATM, and promote browning of white adipose tissue. The TLR4-NF-κB pathway plays a more critical role in promoting the browning of white adipose tissue by regulating macrophage polarization in LH intervention.

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Publication Details

Journal
Scientific Reports
Published
2025-10-28
DOI
https://doi.org/10.1038/s41598-025-21537-x
Citations
2
Primary Topic
Adipose Tissue and Metabolism
Type
article
Field-Weighted Citation Impact
2.33
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article

LLTH induces white adipose tissue browning via NF κB inhibition in ATM

Lianshi Feng, Yingli Lu, Jie Qiu, Junpeng Feng et al.
2 citations
Scientific Reports
Adipose Tissue and Metabolism
2.33
article

LLTH induces white adipose tissue browning via NF κB inhibition in ATM

Lianshi Feng, Yingli Lu, Jie Qiu, Junpeng Feng, Yi Yan
article en
2 citations

Abstract

This study aimed to explore the role of macrophage polarization and TLR4/NF-κB pathway in promoting browning of white adipose tissue through different hypoxic exercises. (1) Fifty obese female rats were selected after 16 weeks of high-fat diet feeding and randomly divided into normoxic sedentary (NC), normoxic exercise (NE), hypoxic sedentary (HC), Living-High Training-High (HH), and Living-Low Training-High (LH) groups. Four weeks of hypoxic and exercise interventions were conducted to investigate changes in the expression of the TLR4/NF-κB pathway and inflammatory factors in obese rat adipose tissue and the expression of genes and proteins related to adipose tissue browning. (2) After the 4-week intervention, adipose tissue macrophages (ATM) were isolated from HH and LH groups, activated with NF-κB activator, and co-cultured with adipocyte-induced adipose-derived stem cells to explore the role of the TLR4/NF-κB pathway in promoting browning of white adipose tissue by inducing changes in macrophage polarization through different hypoxic exercise. (1) After 4 weeks of different hypoxic interventions, the proportion of M1 macrophages decreased (p < 0.01), and HH intervention increased the proportion of M2 macrophages (p < 0.05). The protein expression levels of TLR4, NF-κB, p-NF-κB, and MyD88 in ATM of the HH and LH groups were significantly lower than those of the NC group (p < 0.01). Four weeks of LH intervention significantly upregulated the protein expression levels of CIDEA, C/EBP-β, PPAR-γ, PGC-1α, PRDM-16, and UCP-1 in rat adipose tissue (p < 0.01). (2) NF-κB activator intervention for 24 h significantly upregulated the protein expression levels of TLR4, p-NF-κB, and MyD88 in adipose tissue of HH and LH group rats (p < 0.01). NF-κB activator intervention for 24 h downregulated the protein expression levels of CIDEA, C/EBP-β, PPAR-γ, PGC-1α, PRDM-16, and UCP-1 in co-cultured adipocytes for 48 h in ATM of the LH group rats (p < 0.05). Four weeks of HH and LH interventions could reduce M1 polarization of ATM, downregulate the expression levels of the TLR4-NF-κB pathway in ATM, and promote browning of white adipose tissue. The TLR4-NF-κB pathway plays a more critical role in promoting the browning of white adipose tissue by regulating macrophage polarization in LH intervention.

Scientific ReportsVol. 15(1)
General Administration of Sport of China (CN), China Institute of Sport Science (CN), Beijing Sport University (CN)
Openalex Percentile: Top 10%
Adipose Tissue and Metabolism
2.33
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