Effects of multi-organ crosstalk on the physiology and pathology of adipose tissue

Front Endocrinol (Lausanne). 2023 Jun 13:14:1198984. doi: 10.3389/fendo.2023.1198984. eCollection 2023.

Abstract

In previous studies, adipocytes were found to play an important role in regulating whole-body nutrition and energy balance, and are also important in energy metabolism, hormone secretion, and immune regulation. Different adipocytes have different contributions to the body, with white adipocytes primarily storing energy and brown adipocytes producing heat. Recently discovered beige adipocytes, which have characteristics in between white and brown adipocytes, also have the potential to produce heat. Adipocytes interact with other cells in the microenvironment to promote blood vessel growth and immune and neural network interactions. Adipose tissue plays an important role in obesity, metabolic syndrome, and type 2 diabetes. Dysfunction in adipose tissue endocrine and immune regulation can cause and promote the occurrence and development of related diseases. Adipose tissue can also secrete multiple cytokines, which can interact with organs; however, previous studies have not comprehensively summarized the interaction between adipose tissue and other organs. This article reviews the effect of multi-organ crosstalk on the physiology and pathology of adipose tissue, including interactions between the central nervous system, heart, liver, skeletal muscle, and intestines, as well as the mechanisms of adipose tissue in the development of various diseases and its role in disease treatment. It emphasizes the importance of a deeper understanding of these mechanisms for the prevention and treatment of related diseases. Determining these mechanisms has enormous potential for identifying new targets for treating diabetes, metabolic disorders, and cardiovascular diseases.

Keywords: adipocyte; adipose tissue; crosstalk; diabetes; obesity; organs.

Publication types

  • Review
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adipocytes, Brown
  • Adipose Tissue
  • Cell Physiological Phenomena
  • Diabetes Mellitus, Type 2*
  • Humans
  • Nutritional Status

Grants and funding

This work was supported by National Natural Science Foundation of China (81971329) and Natural Science Foundation of Guangdong Province (2021A1515012236). Scientific Cooperation Project of Clinic Plus of Affiliated Hospital of GDMU (CLP2021B011).