Posted by Our bodies can maintain body temperature in cold environments. However, the detailed mechanism remains unclear. Researchers from University of Tsukuba elucidated the molecular mechanism by which macrophages, a type of immune cells, control heat production in brown adipose tissue to increase the body temperature in response to cold.
Maintaining body temperature in cold environments is critical for survival. However, the detailed mechanisms remain elusive. The body employs two methods for heat production: shivering-mediated heat production by skeletal muscle and non-shivering thermogenesis by brown adipose tissue. The latter is particularly significant for long-term adaptation to cold.
Recently, researchers investigated the role of the transcription factor MAFB in macrophages — an immune cell type involved in non-shivering thermogenesis within brown adipose tissue. This tissue can generate heat to increase the body temperature in response to cold, primarily regulated by the sympathetic nervous system. Therefore, the researchers bred Mafb-deficient mice and exposed them to cold conditions, monitoring their body temperature changes. They found that heat production by brown adipose tissue was reduced in Mafb-deficient mice, leading to a decrease in body temperature. Additionally, the density of sympathetic nerve fibers in the brown adipose tissue of Mafb-deficient mice was notably lower than that in wild-type mice. Further analysis revealed that MAFB inhibits the expression of the inflammatory cytokine IL-6, consequently reducing the expression of nerve growth factor in brown adipose tissue and impairing the development of sympathetic nerve fibers. These results suggest that MAFB-mediated regulation of sympathetic nerve fiber density plays a key role in the thermogenic capacity of brown adipose tissue.
These findings contribute to a novel understanding of how body temperature maintenance is associated with macrophages, with potential implications for health preservation in cold climates and obesity treatment through enhanced energy expenditure.
This work was supported by the Ministry of Education and Sports of Japan (MEXT); the Ministry of Education, Culture, Sports, Science and Technology of Japan under grants No. 26221004, 25860205, 23118504, 16K18398, 19K07499, and 19H00966, 23K05586, 19K07499; the Uehara Memorial Foundation; the Takeda Science Foundation; the Takamatsunomiya Cancer Foundation under grant No. 15-24724 (M. Hamada); and the World Premier International Research Center Initiative (WPI), MEXT, Japan.