Iron: The silent culprit in your adipose tissue

• Published in: Obesity reviews Vol. 25; no. 1; pp. e13647 - n/a
• Main Authors: Moreno‐Navarrete, José María, Fernández‐Real, José Manuel
• Format: Journal Article
• Language: English
• Published: England Wiley Subscription Services, Inc 01.01.2024
• Subjects: aconitate hydratase; Adipogenesis; Adipose tissue; Adipose tissue (brown); Biological activity; blood serum; Body fat; brown adipose tissue; Ferritin; Homeostasis; inflammation; Insulin resistance; Iron; iron homeostasis; liver; Macrophages; mitochondria; Modulators; Obesity; phenotype; Phenotypes; Skeletal muscle; therapeutics; adipose tissue; iron homeostasis; inflammation; mitochondria
• ISSN: 1467-7881; 1467-789X; 1467-789X
• DOI: 10.1111/obr.13647

Summary Iron plays a vital role in essential biological processes and requires precise regulation within the body. Dysregulation of iron homeostasis, characterized by increased serum ferritin levels and excessive accumulation of iron in the liver, adipose tissue, and skeletal muscle, is associated with obesity and insulin resistance. Notably, iron excess in adipose tissue promotes adipose tissue dysfunction. As optimal adipose tissue function is crucial for maintaining a healthy phenotype in obesity, a comprehensive understanding of iron homeostasis in adipose tissue is imperative for designing new therapeutic approaches to improve and prevent adipose tissue dysfunction. Here, we conducted a review of relevant studies, focusing on and providing valuable insights into the intricate interplay between iron and adipose tissue. It sheds light on the impact of iron on adipogenesis and the physiology of both white and brown adipose tissue. Furthermore, we highlight the critical role of key modulators, such as cytosolic aconitase, mitochondria, and macrophages, in maintaining iron homeostasis within adipose tissue.