Therapeutic targeting of white adipose tissue metabolic dysfunction in obesity: mechanisms and opportunities.
Zi-Han YangFang-Zhou ChenYi-Xiang ZhangMin-Yi OuPoh-Ching TanXue-Wen XuQing-Feng LiShuang-Bai ZhouPublished in: MedComm (2024)
White adipose tissue is not only a highly heterogeneous organ containing various cells, such as adipocytes, adipose stem and progenitor cells, and immune cells, but also an endocrine organ that is highly important for regulating metabolic and immune homeostasis. In individuals with obesity, dynamic cellular changes in adipose tissue result in phenotypic switching and adipose tissue dysfunction, including pathological expansion, WAT fibrosis, immune cell infiltration, endoplasmic reticulum stress, and ectopic lipid accumulation, ultimately leading to chronic low-grade inflammation and insulin resistance. Recently, many distinct subpopulations of adipose tissue have been identified, providing new insights into the potential mechanisms of adipose dysfunction in individuals with obesity. Therefore, targeting white adipose tissue as a therapeutic agent for treating obesity and obesity-related metabolic diseases is of great scientific interest. Here, we provide an overview of white adipose tissue remodeling in individuals with obesity including cellular changes and discuss the underlying regulatory mechanisms of white adipose tissue metabolic dysfunction. Currently, various studies have uncovered promising targets and strategies for obesity treatment. We also outline the potential therapeutic signaling pathways of targeting adipose tissue and summarize existing therapeutic strategies for antiobesity treatment including pharmacological approaches, lifestyle interventions, and novel therapies.
Keyphrases
- insulin resistance
- adipose tissue
- high fat diet induced
- high fat diet
- metabolic syndrome
- polycystic ovary syndrome
- endoplasmic reticulum stress
- weight loss
- induced apoptosis
- low grade
- oxidative stress
- type diabetes
- skeletal muscle
- cardiovascular disease
- signaling pathway
- high grade
- epithelial mesenchymal transition
- climate change
- body mass index
- drug delivery
- cell cycle arrest
- combination therapy
- liver fibrosis