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Chronic inflammation in high-fat diet-fed mice: Unveiling the early pathogenic connection between liver and adipose tissue

  1. Author:
    Bae, Heekyong R
    Shin, Su-Kyung
    Yoo, Ji-Hyeon
    Kim, Suntae
    Young,Howard
    Kwon, Eun-Young
  2. Author Address

    Department of Food Science and Nutrition, Kyungpook National University, Daegu, 41566, Republic of Korea; Center for Food and Nutritional Genomics, Kyungpook National University, Daegu, 41566, Republic of Korea., Omixplus, LLC., Gaithersburg, MD, 20850, USA., Cancer Innovation Laboratory, Center for Cancer Research, National Cancer Institute, Frederick, MD, 21702, USA., Department of Food Science and Nutrition, Kyungpook National University, Daegu, 41566, Republic of Korea; Center for Food and Nutritional Genomics, Kyungpook National University, Daegu, 41566, Republic of Korea. Electronic address: eykwon@knu.ac.kr.,
    1. Year: 2023
    2. Date: Aug 16
    3. Epub Date: 2023 08 16
  1. Journal: Journal of Autoimmunity
    1. 139
    2. Pages: 103091
  2. Type of Article: Article
  3. Article Number: 103091
  1. Abstract:

    Obesity-induced chronic inflammation has been linked to several autoimmune diseases, including rheumatoid arthritis, type 1 diabetes, and multiple sclerosis. The underlying mechanisms are not yet fully understood, but it is believed that chronic inflammation in adipose tissue can lead to the production of pro-inflammatory cytokines and chemokines, which can trigger immune responses and contribute to the development of autoimmune diseases. However, the underlying mechanisms that lead to the infiltration of immune cells into adipose tissue are not fully understood. In this study, we observed a time-dependent response to a high-fat diet in the liver and epididymal white adipose tissue using gene set enrichment analysis. Our findings revealed a correlation between early abnormal innate immune responses in the liver and late inflammatory response in the adipose tissue, that eventually leads to systemic inflammation. Specifically, our data suggest that the dysregulated NADH homeostasis in the mitochondrial matrix, interacting with the mitochondrial translation process, could serve as a sign marking the transition from liver inflammation to adipose tissue inflammation. Taken together, our study provides valuable insights into the molecular mechanisms underlying the development of chronic inflammation and associated autoimmune diseases in obesity. Copyright © 2023 The Authors. Published by Elsevier Ltd.. All rights reserved.

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External Sources

  1. DOI: 10.1016/j.jaut.2023.103091
  2. PMID: 37595410
  3. PII : S0896-8411(23)00100-2

Library Notes

  1. Fiscal Year: FY2022-2023
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