Cell-cell crosstalk between fat cells and immune cells.
adipose tissue
cytokines
immune cells
obesity
thermogenesis
Journal
American journal of physiology. Endocrinology and metabolism
ISSN: 1522-1555
Titre abrégé: Am J Physiol Endocrinol Metab
Pays: United States
ID NLM: 100901226
Informations de publication
Date de publication:
31 Jul 2024
31 Jul 2024
Historique:
medline:
31
7
2024
pubmed:
31
7
2024
entrez:
31
7
2024
Statut:
aheadofprint
Résumé
Obesity is a metabolic disorder with pandemic-like implications, lacking viable pharmaceutical treatments currently. Thermogenic adipose tissues, including brown and beige adipose tissues, play an essential role in regulating systemic energy homeostasis and have emerged as appealing therapeutic targets for the treatment of obesity and obesity-related diseases. The function of adipocytes is subject to the complex regulation by a cellular network of immune signaling pathways in response to environmental signals. However, the specific regulatory roles of immune cells in thermogenesis and relevant involving mechanisms are still not well understood. Here, we concentrate on our present knowledge of the interaction between thermogenic adipocytes and immune cells, present an overview of cellular and molecular mechanisms underlying immunometabolism in adipose tissues. We discuss cytokines, especially interleukins, which are originated from widely variable sources and their impacts on the development and function of thermogenic adipocytes. Moreover, we summarize the neuro-immune regulation in heat production and expand a new mode of intercellular communication mediated by mitochondrial transfer. The crosstalk between immune cells and adipocytes achieves adipose tissue homeostasis and systemic energy balance. A deep understanding of this intricate interaction would provide evidence on improving thermogenic efficiency by remodeling the immune microenvironment. Interventions based on these factors show high potential to prevent adverse metabolic outcomes in obese patients.
Identifiants
pubmed: 39082899
doi: 10.1152/ajpendo.00024.2024
doi:
Types de publication
Journal Article
Review
Langues
eng
Sous-ensembles de citation
IM
Subventions
Organisme : MOST | National Natural Science Foundation of China (NSFC)
ID : 82070859
Organisme : MOST | National Natural Science Foundation of China (NSFC)
ID : 82270910
Organisme : Tongji Hospital (TJH)
ID : 2201103295