Transcription regulators and hormones involved in the development of brown fat and white fat browning: transcriptional and hormonal control of brown/beige fat development
Language English Country Czech Republic Media print-electronic
Document type Journal Article, Review
PubMed
29527907
DOI
10.33549/physiolres.933650
PII: 933650
Knihovny.cz E-resources
- MeSH
- Adipose Tissue, White cytology physiology MeSH
- Cell Differentiation MeSH
- Adipose Tissue, Brown cytology growth & development MeSH
- Hormones metabolism MeSH
- Humans MeSH
- Gene Expression Regulation MeSH
- Transcription Factors metabolism MeSH
- Animals MeSH
- Check Tag
- Humans MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Review MeSH
- Names of Substances
- Hormones MeSH
- Transcription Factors MeSH
The high prevalence of obesity and related metabolic complications has inspired research on adipose tissues. Three kinds of adipose tissues are identified in mammals: brown adipose tissue (BAT), beige or brite adipose tissue and white adipose tissue (WAT). Beige adipocytes share some characteristics with brown adipocytes such as the expression of UCP1. Beige adipocytes can be activated by environmental stimuli or pharmacological treatment, and this change is accompanied by an increase in energy consumption. This process is called white browning, and it facilitates the maintenance of a lean and healthy phenotype. Thus, promoting beige adipocyte development in WAT shows promise as a new strategy in treating obesity and related metabolic consequences. In this review, we summarized the current understanding of the regulators and hormones that participate in the development of brown fat and white fat browning.
References provided by Crossref.org
Fibroblast growth factor 21 (FGF21) in children and adolescents with chronic kidney disease